Deck 14: Dna Structure, Replication, and Organization

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Question
The T2 bacteriophages used in the Hershey and Chase experiment contain ____.

A) DNA only
B) RNA and protein
C) protein, phospholipid, and DNA
D) DNA and protein
E) protein, phospholipid, DNA, and RNA
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Question
The genome of an organism contains 30% adenine. Based on this, you would predict that this organism's genome also contains 30% ____.

A) thymine
B) cytosine
C) each of cytosine and guanine
D) each of thymine and guanine
E) guanine
Question
The genetic material of all living organisms is ____.

A) protein
B) deoxyribonucleic acid
C) ribonucleic acid
D) glycoprotein
E) polypeptide
Question
In the Hershey and Chase experiment,32P was used to label ____ and35S was used to label ____.

A) RNA; protein
B) protein; DNA
C) phospholipids; protein
D) protein; phospholipids
E) DNA; protein
Question
If a stretch of human double-stranded DNA contains 47% G and C bases, then ____.

A) it contains 47% A and T bases
B) there are more pyrimidines than purines
C) there are more purines than pyrimidines
D) it contains 53% A and T bases
E) there are no genes in this stretch of DNA
Question
The transforming principle described by Griffith in his work with Streptococcus pneumoniae was later shown by Avery, MacLeod, and McCarty to be ____.

A) a polysaccharide capsule
B) a phospholipid
C) protein
D) RNA
E) DNA
Question
James Watson, Francis Crick, Rosalind Franklin, and Maurice Wilkins are recognized for their contributions to the discovery of the ____.

A) presence of nuclein (DNA) in white blood cells
B) role of DNA in cells
C) chemical components of DNA
D) three-dimensional structure of DNA
E) location of DNA in cells
Question
What happens when living R strain Streptococcus pneumoniae bacteria are mixed with heat-killed S strain Streptococcus pneumoniae bacteria?

A) The S strain bacteria come back to life.
B) The R strain bacteria are killed, and the S strain bacteria remain dead.
C) The R strain bacteria are transformed into S strain bacteria.
D) The S strain bacteria are transformed into R strain bacteria.
E) The R strain bacteria are killed, and the S strain bacteria come back to life.
Question
Adjacent nucleotides on a strand of DNA are connected to each other by a(n) ____.

A) hydrophobic interaction
B) phosphodiester bond
C) hydrogen bond
D) peptide bond
E) ionic bond
Question
In the Hershey and Chase experiment, phage-infected bacteria and viral progeny were radioactive following bacterial infection with32P-labeled viruses. Why?

A) Bacteria had incorporated radioactive proteins into their DNA.
B) Phage DNA labeled with32P had entered the bacteria and appeared in progeny phages.
C) Viral progeny had used the32P to build new viral proteins.
D) Bacteria had incorporated radioactive proteins into their cell membranes.
E)32P was left outside the cell during viral infection.
Question
Avery, MacLeod, and McCarty continued Griffith's work with S. pneumoniae and concluded that DNA was the hereditary material. If protein were the hereditary material instead of DNA, what would happen to mice after injection of heat-killed virulent bacteria mixed with live non-virulent bacteria after treatment with protease?

A) The mice would live.
B) The mice would die.
C) The mice would get sick, but recover.
D) The mice would grow tumors.
E) The mice would degrade the protein.
Question
Prior to the 1940s, many biologists believed ____, which is composed of 20 different types of ____, was most likely the genetic material.

A) protein; amino acids
B) DNA; amino acids
C) protein; nucleotides
D) DNA; nucleotides
E) RNA; nucleotides
Question
Nucleic acids are long chains of ____.

A) amino acids
B) lipids
C) nucleotides
D) sugars
E) peptides
Question
The genome of an organism contains 14% guanine; therefore, its genome also contains ____% thymine and ____% cytosine.

A) 86; 14
B) 14; 36
C) 36; 36
D) 14; 86
E) 36; 14
Question
When Hershey and Chase labeled viruses with radioactive phosphorus, they concluded that the virus injects DNA and not protein into its host because ____.

A) most of the radioactive protein was inside the bacteria
B) most of the radioactive DNA, but little protein ,was inside the bacteria
C) both radioactive DNA and protein were inside the bacteria
D) neither radioactive DNA nor protein was inside the bacteria
E) entire viruses were inside the bacteria
Question
Each DNA nucleotide is composed of ____.

A) a six-carbon sugar, a phosphate group, and one of twenty amino acids
B) a five-carbon sugar, a nitrogenous base, and one of twenty amino acids
C) a five-carbon sugar, a phosphate group, and one of four nitrogenous bases
D) a six-carbon sugar, a nitrogenous base, and one of four amino acids
E) a five-carbon sugar, a phosphate group, and one of four amino acids
Question
The alteration of a cell's hereditary type by the uptake of DNA released by the breakdown of another cell is called ____.

A) replication
B) transformation
C) crossing-over
D) excision repair
E) ligation
Question
Suppose that you performed a version of the Hershey and Chase experiment, this time using32P-labeled viruses that insert their double-stranded DNA into the DNA of the cells that they infect. The viral DNA is then treated as part of the cell's own DNA and is replicated during DNA replication and passed onto daughter cells when the cell divides. You infect a population of cells with the32P-labeled viruses, and then let the infected cells go through two generations of cell divisions. If you then examine the cells, you should find32P-labeled DNA in ____ of the cells.

A) none
B)  about 1/4
C) about 1/2
D) about 3/4
E) all
Question
In their experiments to identify the transforming principle, Avery, MacLeod, and McCarty used enzymes that break down ____.

A) protein, DNA, and RNA
B) protein and RNA only
C) DNA only
D) protein, lipids, and RNA
E) lipids and DNA only
Question
Purines and pyrimidines are ____.

A) Okazaki fragments
B) pentose-phosphate backbones
C) nucleic acids
D) phosphate bases
E) nitrogenous bases
Question
The width of a DNA double helix ____.

A) is constant
B) is narrower where adenine is present than where cytosine is present
C) is wider where purines are present than where pyrimidines are present
D) varies randomly
E) is wider where pyrimidines are present than where purines are present
Question
The active site of DNA polymerase is similar in ____.

A) archaea and bacteria only
B) archaea, bacteria, and eukaryotes
C) archaea and eukaryotes only
D) none of these groups
E) bacteria and eukaryotes only
Question
In DNA, the pyrimidines are ____.

A) thymine and cytosine
B) adenine and cytosine
C) adenine and guanine
D) thymine and adenine
E) guanine and thymine
Question
Why is DNA ligase most active on the lagging strand during DNA replication?

A) The lagging strands contain more short DNA segments, which are joined together by DNA ligase, than the leading strand.
B) The lagging strand is synthesized more slowly, and DNA ligase speeds up the DNA polymerase.
C) The lagging strand synthesizes DNA in the 3' ->5' direction.
D) The lagging strand requires DNA ligase to couple the RNA primer to the Okazaki fragments.
E) DNA ligase performs the function of RNA primase on the lagging strand.
Question
The polynucleotide chain of DNA has polarity: the 5' end has a bound ____, while the 3' end has a bound ____.

A) deoxyribose sugar, ribose sugar
B) adenine, thymine
C) cytosine, guanine
D) hydroxyl group, phosphate group
E) phosphate group, hydroxyl group
Question
DNA polymerase ____.

A) synthesizes a short RNA segment to begin DNA replication
B) adds nucleotides to the 5' end of an existing strand to synthesize a new DNA strand
C) adds nucleotides to the 3' end of an existing strand to synthesize a new DNA strand
D) seals nicks between adjacent segments of DNA
E) unwinds the DNA double helix at the origin of replication
Question
How are purines distinguished from pyrimidines?

A) Purines are derived from a pair of fused C-N rings, while pyrimidines are derived from a single C-N ring.
B) Pyrimidines are derived from a pair of fused C-N rings, while purines are derived from a single C-N ring.
C) Purines have a carbon-containing ring, while pyrimidines have a nitrogenous ring.
D) Pyrimidines have a carbon-containing ring, while purines have a nitrogenous ring.
E) Purines are found only in DNA, while pyrimidines are found only in RNA.
Question
Topoisomerase functions by ____.

A) creating cuts in the DNA to relieve over-twisting and strain ahead of the replication fork
B) binding DNA polymerase to hold it tightly to the template DNA
C) unwinding the DNA double helix to expose the template strands for replication
D) binding the newly synthesized DNA to re-twist it into a double helix after replication
E) reading the DNA template and synthesizing a complementary strand of DNA
Question
<strong>  Figure 14.1 The accompanying figure depicts the result of an experiment to determine how DNA replication occurs. Based on these results, it appears that after replication, each new DNA molecule contains ____.</strong> A) either entirely old DNA strands or entirely new DNA strands B) one old DNA strand and one new DNA strand C) entirely new DNA D) some DNA helix regions from old DNA alternating with some DNA regions from new DNA E) two strands that are each a mix of old and new DNA <div style=padding-top: 35px> Figure 14.1
The accompanying figure depicts the result of an experiment to determine how DNA replication occurs. Based on these results, it appears that after replication, each new DNA molecule contains ____.

A) either entirely old DNA strands or entirely new DNA strands
B) one old DNA strand and one new DNA strand
C) entirely new DNA
D) some DNA helix regions from old DNA alternating with some DNA regions from new DNA
E) two strands that are each a mix of old and new DNA
Question
Helicase ____.

A) proofreads the newly synthesized DNA
B) relieves over-twisting ahead of the DNA replication fork
C) rewinds the newly synthesized DNA strands into a double-stranded helix
D) unwinds the double-stranded DNA helix
E) binds DNA polymerase to the template strand
Question
A DNA double helix has two strands that are held together by ____.

A) hydrogen bonds
B) ionic bonds
C) hydrophobic interactions
D) phosphodiester bonds
E) covalent bonds
Question
DNA replication is said to be semiconservative because ____.

A) the number of nucleotides within genes remains constant
B) half of the DNA in a cell comes from one parent, and the other half from the other parent.
C) the same process of DNA replication is used by all organisms
D) the total amount of DNA within an individual remains the same
E) each new DNA molecule is composed of one old strand and one new strand
Question
Which nucleotide sequence is complementary to the DNA sequence 5'-GACGTT-3'?

A) 5'-TCATGG-3'
B) 3'-TCATGG-5'
C) 3'-CTGCAA-5'
D) 3'-AGTACC-5'
E) 5'-TTGCAG-3'
Question
DNA ligase closes nicks between ____ by forming ____ bonds.

A) nitrogenous bases; hydrogen
B) RNA fragments; noncovalent
C) DNA and RNA fragments; covalent
D) DNA fragments; peptide
E) DNA fragments; covalent
Question
In the Meselson-Stahl experiment, bacterial DNA was labeled completely with heavy nitrogen (15N) and then grown in the presence of light nitrogen (14N). When only mixed DNA was observed after ONE generation of growth in14N, what was the conclusion?

A) DNA replication is semiconservative
B) DNA replication is conservative
C) DNA replication is dispersive
D) DNA replication is either semiconservative or dispersive
E) DNA replication is either semiconservative or conservative
Question
The two strands of a DNA double helix are said to be antiparallel. This means that ____.

A) the 5' end of one strand is directly paired with the 5' end of the other strand
B) since the double helix twists, it is not perfectly parallel
C) one strand has a negative charge, and the other strand has a positive charge
D) the 5' end of one strand is directly paired with the 3' end of the other strand
E) both strands have a negative charge
Question
A short RNA chain is synthesized as the first nucleotides in a new DNA strand by the enzyme ____ to provide a ____ for DNA elongation.

A) topoisomerase; 3' hydroxyl group
B) primase; 3' hydroxyl group
C) primase; 5' hydroxyl group
D) DNA polymerase; 5' phosphate group
E) DNA polymerase; 3' hydroxyl group
Question
Which statement correctly describes DNA base pairing?

A) Two hydrogen bonds bind A and T; three hydrogen bonds bind G and C.
B) Two hydrogen bonds bind A and C; three hydrogen bonds bind T and G.
C) Two hydrogen bonds bind G and C; three hydrogen bonds bind A and T.
D) Two hydrogen bonds bind A and T, and two hydrogen bonds bind G and C.
E) Three hydrogen bonds bind A and C, and three hydrogen bonds bind T and G.
Question
In DNA, the purines are ____.

A) thymine and cytosine
B) adenine and cytosine
C) adenine and guanine
D) thymine and adenine
E) guanine and thymine
Question
Wilkins and Franklin studied the structure of DNA using ____.

A) molecular scale models of nucleotides
B) X-ray diffraction
C) computer-assisted graphics
D) electron microscopy
E) light microscopy
Question
During DNA replication, nucleosomes must ____ ahead of the replication fork and ____ after DNA is replicated.

A) disassemble; reassemble
B) reassemble; disassemble
C) unwind DNA; disassociate
D) synthesize primers; proofread
E) cut DNA; ligate DNA
Question
In humans, telomerase ____.

A) adds telomere repeats in some human cells
B) removes telomere repeats in all human cells
C) adds telomere repeats in all human cells
D) removes telomere repeats in some human cells
E) transcribes telomere repeats in some human cells
Question
During normal DNA replication, part of the sequence at the ends of linear chromosomes is not copied into the new DNA strands because ____.

A) DNA ligase cannot join pieces at the end of a chromosome
B) RNA primers at the beginning of a new strand cannot be replaced with DNA
C) those ends are Okazaki fragments that are lost
D) cells do not need the DNA at the ends of chromosomes
E) the ends of chromosomes are made of protein, not DNA
Question
Reiji Okazaki discovered what are now called "Okazaki fragments" produced during DNA replication. These fragments are ____.

A) short lengths of new DNA on the leading strand
B) RNA primers on the lagging strand
C) RNA primers on both the lagging and leading strand
D) short lengths of new DNA on the lagging strand
E) RNA primers on the leading strand
Question
Proofreading by ____ corrects errors that occur during DNA replication.

A) DNA polymerase
B) primase
C) telomerase
D) DNA ligase
E) helicase
Question
The nucleosome core particle consists of ____.

A) two chromosomes linked together
B) RNA wrapped around an eight-protein histone complex
C) DNA wrapped around an eight-protein histone complex
D) DNA associated with the nuclear envelope
E) DNA replication enzymes associating to form the replisome
Question
Individuals with xeroderma pigmentosum inherit a faulty DNA repair mechanism. As a consequence, ____.

A) they are sterile
B) their cells have no proofreading abilities during DNA replication
C) Okazaki fragments produced during DNA replication cannot be joined
D) they easily develop skin cancer when exposed to sunlight
E) their telomeres are shorter than average
Question
The energy to form the new bonds between nucleotides in a growing DNA strand is provided primarily by ____.

A) unwinding of the DNA double helix
B) hydrolysis of pyrophosphate
C) breaking hydrogen bonds between base pairs
D) DNA helicase
E) forming hydrogen bonds between base pairs
Question
Imagine that a cell contains a genetic mutation in the gene encoding the primase enzyme, rendering it unable to synthesize RNA strands. Assuming that all of the other enzymes directly involved in DNA replication are still functional in these cells, how much of the DNA replication process would you expect to see in these cells?

A) The leading strand would be synthesized, but not the lagging strand.
B) No part of the DNA replication process could occur.
C) The DNA helix would be unwound by helicase, but no new strands will be produced.
D) Both the leading and lagging strand would be synthesized, but pieces of discontinuous strands would not be joined together.
E) DNA replication would still proceed completely since RNA strands are not part of the final product of DNA replication.
Question
Telomeres are found ____.

A) in the middle of chromosomes
B) at replication origins
C) where DNA strands are joined together
D) within genes
E) at the ends of chromosomes
Question
Adding nucleotides onto a growing DNA strand during DNA replication in cells occurs in ____.

A) the 5' ->3' direction for the leading strand and the 3' ->5' direction on the lagging strand
B) either the 5' ->3' direction or the 3' ->5' direction on both strands, depending on where replication begins
C) the 5' ->3' direction only
D) the 3' ->5' direction for the leading strand and the 5' ->3' direction on the lagging strand
E) the 3' ->5' direction only
Question
Nucleosomes are best described as ____.

A) prokaryotic DNA associated with nonhistone proteins
B) eukaryotic DNA associated with histone proteins
C) prokaryotic DNA associated with histone proteins
D) eukaryotic DNA associated with nonhistone proteins
E) associated histone and nonhistone proteins
Question
When DNA is replicated, ____.

A) parental histones are degraded and entirely replaced by new histones
B) DNA is permanently freed from histone binding
C) new histone proteins are also produced
D) new histone proteins are not needed
E) the number of histones that bind to each DNA molecule is halved
Question
In eukaryotes, the DNA molecule that comprises a chromosome is ____ and has ____ replication origin.

A) circular, one
B) circular, more than one
C) linear, more than one
D) linear, one
E) linear, no
Question
The components of nucleosomes is(are) ____.

A) DNA only
B) DNA, RNA, and protein
C) DNA and RNA
D) RNA and protein
E) DNA and protein
Question
Without proofreading, the rate of DNA replication errors in bacteria and eukaryotes is as high as one for every ____ nucleotides assembled.

A) 10 to 100
B) 100,000 to 1,000,000
C) 1,000 to 10,000
D) 10,000,000 to 100,000,000
E) 100,000,000 to 1,000,000,000
Question
After DNA repair enzymes remove an incorrect nucleotide resulting from a replication error, ____ is/are needed to complete the repair.

A) primase, DNA polymerase, and DNA ligase
B) DNA polymerase
C) DNA polymerase and DNA ligase
D) primase and DNA ligase
E) primase and DNA polymerase
Question
In prokaryotes, the DNA molecule that makes up a chromosome is ____ and has ____ replication origin.

A) circular; one
B) circular; more than one
C) linear; more than one
D) linear; one
E) linear; no
Question
Suppose you take a cell from an adult cow and attempt to use it to produce a clone of that cow. If telomerase is not functioning in that cell or in any of the cell's progeny, what would you expect to happen to your clone?

A) The clone will be unable to grow.
B) When the clone matures, it will most likely have cancer.
C) The clone's cells may divide, but after a certain number of generations, cell division will stop.
D) The lack of telomerase should have no effect on the clone.
E) When the clone matures, it will most likely be sterile.
Question
During DNA replication, the ____ strand is assembled in the ____ direction as helix unwinding and is synthesized by ____ replication.

A) leading; opposite; continuous
B) lagging; same; discontinuous
C) leading; same; discontinuous
D) lagging; opposite; continuous
E) leading; same; continuous
Question
Match between columns
Point at which the double helix begins unwinding
leading strand
Point at which the double helix begins unwinding
replication fork
Point at which the double helix begins unwinding
origin of replication
Point at which the double helix begins unwinding
replisome
Point at which the double helix begins unwinding
replication bubble
Point at which the double helix begins unwinding
lagging strand
Point at which the double helix begins unwinding
double helix
The strand synthesized in the opposite direction to the movement of the replication fork
leading strand
The strand synthesized in the opposite direction to the movement of the replication fork
replication fork
The strand synthesized in the opposite direction to the movement of the replication fork
origin of replication
The strand synthesized in the opposite direction to the movement of the replication fork
replisome
The strand synthesized in the opposite direction to the movement of the replication fork
replication bubble
The strand synthesized in the opposite direction to the movement of the replication fork
lagging strand
The strand synthesized in the opposite direction to the movement of the replication fork
double helix
The strand synthesized in the direction the replication fork moves
leading strand
The strand synthesized in the direction the replication fork moves
replication fork
The strand synthesized in the direction the replication fork moves
origin of replication
The strand synthesized in the direction the replication fork moves
replisome
The strand synthesized in the direction the replication fork moves
replication bubble
The strand synthesized in the direction the replication fork moves
lagging strand
The strand synthesized in the direction the replication fork moves
double helix
Forms as a result of two replication forks being produced at the origin of replication
leading strand
Forms as a result of two replication forks being produced at the origin of replication
replication fork
Forms as a result of two replication forks being produced at the origin of replication
origin of replication
Forms as a result of two replication forks being produced at the origin of replication
replisome
Forms as a result of two replication forks being produced at the origin of replication
replication bubble
Forms as a result of two replication forks being produced at the origin of replication
lagging strand
Forms as a result of two replication forks being produced at the origin of replication
double helix
Y-shape produced by the unwinding of the DNA double-helix
leading strand
Y-shape produced by the unwinding of the DNA double-helix
replication fork
Y-shape produced by the unwinding of the DNA double-helix
origin of replication
Y-shape produced by the unwinding of the DNA double-helix
replisome
Y-shape produced by the unwinding of the DNA double-helix
replication bubble
Y-shape produced by the unwinding of the DNA double-helix
lagging strand
Y-shape produced by the unwinding of the DNA double-helix
double helix
The structure of DNA
leading strand
The structure of DNA
replication fork
The structure of DNA
origin of replication
The structure of DNA
replisome
The structure of DNA
replication bubble
The structure of DNA
lagging strand
The structure of DNA
double helix
Complex of DNA replication enzymes
leading strand
Complex of DNA replication enzymes
replication fork
Complex of DNA replication enzymes
origin of replication
Complex of DNA replication enzymes
replisome
Complex of DNA replication enzymes
replication bubble
Complex of DNA replication enzymes
lagging strand
Complex of DNA replication enzymes
double helix
Question
Match between columns
Tethers DNA polymerase to the template DNA
single-stranded binding proteins
Tethers DNA polymerase to the template DNA
DNA polymerase III
Tethers DNA polymerase to the template DNA
DNA ligase
Tethers DNA polymerase to the template DNA
helicase
Tethers DNA polymerase to the template DNA
topoisomerase
Tethers DNA polymerase to the template DNA
sliding clamp
Tethers DNA polymerase to the template DNA
primase
Tethers DNA polymerase to the template DNA
DNA polymerase I
Main enzyme that extends RNA primer by adding DNA nucleotides to it
single-stranded binding proteins
Main enzyme that extends RNA primer by adding DNA nucleotides to it
DNA polymerase III
Main enzyme that extends RNA primer by adding DNA nucleotides to it
DNA ligase
Main enzyme that extends RNA primer by adding DNA nucleotides to it
helicase
Main enzyme that extends RNA primer by adding DNA nucleotides to it
topoisomerase
Main enzyme that extends RNA primer by adding DNA nucleotides to it
sliding clamp
Main enzyme that extends RNA primer by adding DNA nucleotides to it
primase
Main enzyme that extends RNA primer by adding DNA nucleotides to it
DNA polymerase I
Unwinds DNA helix
single-stranded binding proteins
Unwinds DNA helix
DNA polymerase III
Unwinds DNA helix
DNA ligase
Unwinds DNA helix
helicase
Unwinds DNA helix
topoisomerase
Unwinds DNA helix
sliding clamp
Unwinds DNA helix
primase
Unwinds DNA helix
DNA polymerase I
Stabilizes single-stranded DNA
single-stranded binding proteins
Stabilizes single-stranded DNA
DNA polymerase III
Stabilizes single-stranded DNA
DNA ligase
Stabilizes single-stranded DNA
helicase
Stabilizes single-stranded DNA
topoisomerase
Stabilizes single-stranded DNA
sliding clamp
Stabilizes single-stranded DNA
primase
Stabilizes single-stranded DNA
DNA polymerase I
Relieves over-winding of DNA ahead of the replication fork
single-stranded binding proteins
Relieves over-winding of DNA ahead of the replication fork
DNA polymerase III
Relieves over-winding of DNA ahead of the replication fork
DNA ligase
Relieves over-winding of DNA ahead of the replication fork
helicase
Relieves over-winding of DNA ahead of the replication fork
topoisomerase
Relieves over-winding of DNA ahead of the replication fork
sliding clamp
Relieves over-winding of DNA ahead of the replication fork
primase
Relieves over-winding of DNA ahead of the replication fork
DNA polymerase I
Synthesizes short RNA segment to initiate new DNA strand
single-stranded binding proteins
Synthesizes short RNA segment to initiate new DNA strand
DNA polymerase III
Synthesizes short RNA segment to initiate new DNA strand
DNA ligase
Synthesizes short RNA segment to initiate new DNA strand
helicase
Synthesizes short RNA segment to initiate new DNA strand
topoisomerase
Synthesizes short RNA segment to initiate new DNA strand
sliding clamp
Synthesizes short RNA segment to initiate new DNA strand
primase
Synthesizes short RNA segment to initiate new DNA strand
DNA polymerase I
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
single-stranded binding proteins
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
DNA polymerase III
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
DNA ligase
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
helicase
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
topoisomerase
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
sliding clamp
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
primase
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
DNA polymerase I
Seals nicks between adjacent DNA segments
single-stranded binding proteins
Seals nicks between adjacent DNA segments
DNA polymerase III
Seals nicks between adjacent DNA segments
DNA ligase
Seals nicks between adjacent DNA segments
helicase
Seals nicks between adjacent DNA segments
topoisomerase
Seals nicks between adjacent DNA segments
sliding clamp
Seals nicks between adjacent DNA segments
primase
Seals nicks between adjacent DNA segments
DNA polymerase I
Question
Match between columns
Showed that DNA replication in Escherichia coli is semiconservative
Avery, MacLeod, and McCarty
Showed that DNA replication in Escherichia coli is semiconservative
Meselson and Stahl
Showed that DNA replication in Escherichia coli is semiconservative
Griffith
Showed that DNA replication in Escherichia coli is semiconservative
Watson and Crick
Showed that DNA replication in Escherichia coli is semiconservative
Hershey and Chase
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Avery, MacLeod, and McCarty
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Meselson and Stahl
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Griffith
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Watson and Crick
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Hershey and Chase
Showed that the genetic material of bacteriophage T2 is DNA
Avery, MacLeod, and McCarty
Showed that the genetic material of bacteriophage T2 is DNA
Meselson and Stahl
Showed that the genetic material of bacteriophage T2 is DNA
Griffith
Showed that the genetic material of bacteriophage T2 is DNA
Watson and Crick
Showed that the genetic material of bacteriophage T2 is DNA
Hershey and Chase
Worked out the double helix model for DNA structure
Avery, MacLeod, and McCarty
Worked out the double helix model for DNA structure
Meselson and Stahl
Worked out the double helix model for DNA structure
Griffith
Worked out the double helix model for DNA structure
Watson and Crick
Worked out the double helix model for DNA structure
Hershey and Chase
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Avery, MacLeod, and McCarty
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Meselson and Stahl
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Griffith
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Watson and Crick
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Hershey and Chase
Question
Match between columns
primase
A
primase
C
primase
E
primase
B
primase
D
DNA polymerase III
A
DNA polymerase III
C
DNA polymerase III
E
DNA polymerase III
B
DNA polymerase III
D
topoisomerase
A
topoisomerase
C
topoisomerase
E
topoisomerase
B
topoisomerase
D
helicase
A
helicase
C
helicase
E
helicase
B
helicase
D
single-stranded binding protein
A
single-stranded binding protein
C
single-stranded binding protein
E
single-stranded binding protein
B
single-stranded binding protein
D
Question
Although Watson and Crick are credited with the discovery of the structure of DNA, they based this discovery on the bench work of many other scientists of the time. Name at least three different pieces of knowledge that Watson and Crick used in their discovery that was based on work from other scientists.
Question
Cancer treatments may specifically target rapidly dividing cells by using drugs or chemicals that ____.

A) promote DNA replication only
B) inhibit DNA repair enzymes only
C) inhibit DNA replication only
D) promote DNA replication or inhibit DNA repair enzymes
E) inhibit DNA replication or DNA repair enzymes
Question
Variability in offspring is largely a result of ____.

A) mutations
B) nucleosomes
C) Okazaki fragments
D) DNA repairs
E) RNA primers
Question
The steps of DNA replication and the enzymes involved are largely conserved amongst bacteria, archaea, and eukaryotes. How can this evolutionary conservation be explained?
Question
Avery, MacLeod, and McCarty showed that DNA was the transforming principle by demonstrating that mice survived when injected with a mixture of dead virulent bacteria and live nonvirulent bacteria that were treated with a DNA degrading enzyme. If RNA was the genetic material, what would have been the effect on the mice? Why?
Question
In many cancers, the cancerous cells have fully active telomerase enzymes. Explain how this might play a role in enabling cancer cells to keep rapidly dividing.
Question
In Hershey and Chase's experiment, why would it not have been suitable to use radioactive nitrogen to label DNA?
Question
Describe what happens to the nucleosome during DNA replication.
Question
Some research has indicated that increased exercise is linked to increased telomere length in renewable tissues, like blood. Assuming that telomerase levels are not increased by exercise, what might explain the increase in telomere length?

A) DNA replication occurred more frequently in individuals who exercised.
B) Cell division occurred more rapidly in individuals who exercised.
C) Telomerase activity was higher in individuals who exercised.
D) Telomerase activity was lower in individuals who exercised.
E) Fewer DNA replication errors occurred in individuals who exercised.
Question
Describe the roles of the following enzymes during DNA replication: ligase, single-stranded binding proteins (SSBs), DNA polymerase III, primase, DNA helicase.
Question
Suppose a DNA replication error is not corrected. After two cell divisions, how many of the four daughter cells contain this mutation (assuming that the mistake was never corrected)?

A) none
B) one
C) two
D) three
E) four
Question
Cancer cells ____.

A) maintain telomerase function
B) have longer telomeres than normal cells
C) eventually die due to shortening chromosomes
D) have circular chromosomes
E) cannot replicate their DNA
Question
What are two main reasons why DNA mutations are so rare?
Question
What is the function of the sliding clamp in DNA replication?

A) unwind DNA ahead of the replication fork
B) anchor DNA polymerase to the template strand
C) remove DNA polymerase from the template strand
D) anchor primase to the template strand
E) bind to single stranded DNA to stabilize it before it is replicated
Question
What is unlikely to happen if the sliding clamp is nonfunctional?

A) The overall rate of DNA synthesis is low.
B) The DNA polymerase and the template strand of DNA are not properly anchored together.
C) The DNA polymerase detaches from the DNA after only a few polymerizations.
D) Many thousands of polymerizations occur before the DNA polymerase detaches.
E) The rate of DNA replication is low.
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Deck 14: Dna Structure, Replication, and Organization
1
The T2 bacteriophages used in the Hershey and Chase experiment contain ____.

A) DNA only
B) RNA and protein
C) protein, phospholipid, and DNA
D) DNA and protein
E) protein, phospholipid, DNA, and RNA
D
2
The genome of an organism contains 30% adenine. Based on this, you would predict that this organism's genome also contains 30% ____.

A) thymine
B) cytosine
C) each of cytosine and guanine
D) each of thymine and guanine
E) guanine
A
3
The genetic material of all living organisms is ____.

A) protein
B) deoxyribonucleic acid
C) ribonucleic acid
D) glycoprotein
E) polypeptide
B
4
In the Hershey and Chase experiment,32P was used to label ____ and35S was used to label ____.

A) RNA; protein
B) protein; DNA
C) phospholipids; protein
D) protein; phospholipids
E) DNA; protein
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5
If a stretch of human double-stranded DNA contains 47% G and C bases, then ____.

A) it contains 47% A and T bases
B) there are more pyrimidines than purines
C) there are more purines than pyrimidines
D) it contains 53% A and T bases
E) there are no genes in this stretch of DNA
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6
The transforming principle described by Griffith in his work with Streptococcus pneumoniae was later shown by Avery, MacLeod, and McCarty to be ____.

A) a polysaccharide capsule
B) a phospholipid
C) protein
D) RNA
E) DNA
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7
James Watson, Francis Crick, Rosalind Franklin, and Maurice Wilkins are recognized for their contributions to the discovery of the ____.

A) presence of nuclein (DNA) in white blood cells
B) role of DNA in cells
C) chemical components of DNA
D) three-dimensional structure of DNA
E) location of DNA in cells
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8
What happens when living R strain Streptococcus pneumoniae bacteria are mixed with heat-killed S strain Streptococcus pneumoniae bacteria?

A) The S strain bacteria come back to life.
B) The R strain bacteria are killed, and the S strain bacteria remain dead.
C) The R strain bacteria are transformed into S strain bacteria.
D) The S strain bacteria are transformed into R strain bacteria.
E) The R strain bacteria are killed, and the S strain bacteria come back to life.
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9
Adjacent nucleotides on a strand of DNA are connected to each other by a(n) ____.

A) hydrophobic interaction
B) phosphodiester bond
C) hydrogen bond
D) peptide bond
E) ionic bond
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10
In the Hershey and Chase experiment, phage-infected bacteria and viral progeny were radioactive following bacterial infection with32P-labeled viruses. Why?

A) Bacteria had incorporated radioactive proteins into their DNA.
B) Phage DNA labeled with32P had entered the bacteria and appeared in progeny phages.
C) Viral progeny had used the32P to build new viral proteins.
D) Bacteria had incorporated radioactive proteins into their cell membranes.
E)32P was left outside the cell during viral infection.
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11
Avery, MacLeod, and McCarty continued Griffith's work with S. pneumoniae and concluded that DNA was the hereditary material. If protein were the hereditary material instead of DNA, what would happen to mice after injection of heat-killed virulent bacteria mixed with live non-virulent bacteria after treatment with protease?

A) The mice would live.
B) The mice would die.
C) The mice would get sick, but recover.
D) The mice would grow tumors.
E) The mice would degrade the protein.
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12
Prior to the 1940s, many biologists believed ____, which is composed of 20 different types of ____, was most likely the genetic material.

A) protein; amino acids
B) DNA; amino acids
C) protein; nucleotides
D) DNA; nucleotides
E) RNA; nucleotides
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13
Nucleic acids are long chains of ____.

A) amino acids
B) lipids
C) nucleotides
D) sugars
E) peptides
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14
The genome of an organism contains 14% guanine; therefore, its genome also contains ____% thymine and ____% cytosine.

A) 86; 14
B) 14; 36
C) 36; 36
D) 14; 86
E) 36; 14
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15
When Hershey and Chase labeled viruses with radioactive phosphorus, they concluded that the virus injects DNA and not protein into its host because ____.

A) most of the radioactive protein was inside the bacteria
B) most of the radioactive DNA, but little protein ,was inside the bacteria
C) both radioactive DNA and protein were inside the bacteria
D) neither radioactive DNA nor protein was inside the bacteria
E) entire viruses were inside the bacteria
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16
Each DNA nucleotide is composed of ____.

A) a six-carbon sugar, a phosphate group, and one of twenty amino acids
B) a five-carbon sugar, a nitrogenous base, and one of twenty amino acids
C) a five-carbon sugar, a phosphate group, and one of four nitrogenous bases
D) a six-carbon sugar, a nitrogenous base, and one of four amino acids
E) a five-carbon sugar, a phosphate group, and one of four amino acids
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17
The alteration of a cell's hereditary type by the uptake of DNA released by the breakdown of another cell is called ____.

A) replication
B) transformation
C) crossing-over
D) excision repair
E) ligation
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18
Suppose that you performed a version of the Hershey and Chase experiment, this time using32P-labeled viruses that insert their double-stranded DNA into the DNA of the cells that they infect. The viral DNA is then treated as part of the cell's own DNA and is replicated during DNA replication and passed onto daughter cells when the cell divides. You infect a population of cells with the32P-labeled viruses, and then let the infected cells go through two generations of cell divisions. If you then examine the cells, you should find32P-labeled DNA in ____ of the cells.

A) none
B)  about 1/4
C) about 1/2
D) about 3/4
E) all
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19
In their experiments to identify the transforming principle, Avery, MacLeod, and McCarty used enzymes that break down ____.

A) protein, DNA, and RNA
B) protein and RNA only
C) DNA only
D) protein, lipids, and RNA
E) lipids and DNA only
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20
Purines and pyrimidines are ____.

A) Okazaki fragments
B) pentose-phosphate backbones
C) nucleic acids
D) phosphate bases
E) nitrogenous bases
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21
The width of a DNA double helix ____.

A) is constant
B) is narrower where adenine is present than where cytosine is present
C) is wider where purines are present than where pyrimidines are present
D) varies randomly
E) is wider where pyrimidines are present than where purines are present
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22
The active site of DNA polymerase is similar in ____.

A) archaea and bacteria only
B) archaea, bacteria, and eukaryotes
C) archaea and eukaryotes only
D) none of these groups
E) bacteria and eukaryotes only
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23
In DNA, the pyrimidines are ____.

A) thymine and cytosine
B) adenine and cytosine
C) adenine and guanine
D) thymine and adenine
E) guanine and thymine
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24
Why is DNA ligase most active on the lagging strand during DNA replication?

A) The lagging strands contain more short DNA segments, which are joined together by DNA ligase, than the leading strand.
B) The lagging strand is synthesized more slowly, and DNA ligase speeds up the DNA polymerase.
C) The lagging strand synthesizes DNA in the 3' ->5' direction.
D) The lagging strand requires DNA ligase to couple the RNA primer to the Okazaki fragments.
E) DNA ligase performs the function of RNA primase on the lagging strand.
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25
The polynucleotide chain of DNA has polarity: the 5' end has a bound ____, while the 3' end has a bound ____.

A) deoxyribose sugar, ribose sugar
B) adenine, thymine
C) cytosine, guanine
D) hydroxyl group, phosphate group
E) phosphate group, hydroxyl group
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26
DNA polymerase ____.

A) synthesizes a short RNA segment to begin DNA replication
B) adds nucleotides to the 5' end of an existing strand to synthesize a new DNA strand
C) adds nucleotides to the 3' end of an existing strand to synthesize a new DNA strand
D) seals nicks between adjacent segments of DNA
E) unwinds the DNA double helix at the origin of replication
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27
How are purines distinguished from pyrimidines?

A) Purines are derived from a pair of fused C-N rings, while pyrimidines are derived from a single C-N ring.
B) Pyrimidines are derived from a pair of fused C-N rings, while purines are derived from a single C-N ring.
C) Purines have a carbon-containing ring, while pyrimidines have a nitrogenous ring.
D) Pyrimidines have a carbon-containing ring, while purines have a nitrogenous ring.
E) Purines are found only in DNA, while pyrimidines are found only in RNA.
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28
Topoisomerase functions by ____.

A) creating cuts in the DNA to relieve over-twisting and strain ahead of the replication fork
B) binding DNA polymerase to hold it tightly to the template DNA
C) unwinding the DNA double helix to expose the template strands for replication
D) binding the newly synthesized DNA to re-twist it into a double helix after replication
E) reading the DNA template and synthesizing a complementary strand of DNA
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29
<strong>  Figure 14.1 The accompanying figure depicts the result of an experiment to determine how DNA replication occurs. Based on these results, it appears that after replication, each new DNA molecule contains ____.</strong> A) either entirely old DNA strands or entirely new DNA strands B) one old DNA strand and one new DNA strand C) entirely new DNA D) some DNA helix regions from old DNA alternating with some DNA regions from new DNA E) two strands that are each a mix of old and new DNA Figure 14.1
The accompanying figure depicts the result of an experiment to determine how DNA replication occurs. Based on these results, it appears that after replication, each new DNA molecule contains ____.

A) either entirely old DNA strands or entirely new DNA strands
B) one old DNA strand and one new DNA strand
C) entirely new DNA
D) some DNA helix regions from old DNA alternating with some DNA regions from new DNA
E) two strands that are each a mix of old and new DNA
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30
Helicase ____.

A) proofreads the newly synthesized DNA
B) relieves over-twisting ahead of the DNA replication fork
C) rewinds the newly synthesized DNA strands into a double-stranded helix
D) unwinds the double-stranded DNA helix
E) binds DNA polymerase to the template strand
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31
A DNA double helix has two strands that are held together by ____.

A) hydrogen bonds
B) ionic bonds
C) hydrophobic interactions
D) phosphodiester bonds
E) covalent bonds
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32
DNA replication is said to be semiconservative because ____.

A) the number of nucleotides within genes remains constant
B) half of the DNA in a cell comes from one parent, and the other half from the other parent.
C) the same process of DNA replication is used by all organisms
D) the total amount of DNA within an individual remains the same
E) each new DNA molecule is composed of one old strand and one new strand
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33
Which nucleotide sequence is complementary to the DNA sequence 5'-GACGTT-3'?

A) 5'-TCATGG-3'
B) 3'-TCATGG-5'
C) 3'-CTGCAA-5'
D) 3'-AGTACC-5'
E) 5'-TTGCAG-3'
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34
DNA ligase closes nicks between ____ by forming ____ bonds.

A) nitrogenous bases; hydrogen
B) RNA fragments; noncovalent
C) DNA and RNA fragments; covalent
D) DNA fragments; peptide
E) DNA fragments; covalent
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35
In the Meselson-Stahl experiment, bacterial DNA was labeled completely with heavy nitrogen (15N) and then grown in the presence of light nitrogen (14N). When only mixed DNA was observed after ONE generation of growth in14N, what was the conclusion?

A) DNA replication is semiconservative
B) DNA replication is conservative
C) DNA replication is dispersive
D) DNA replication is either semiconservative or dispersive
E) DNA replication is either semiconservative or conservative
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36
The two strands of a DNA double helix are said to be antiparallel. This means that ____.

A) the 5' end of one strand is directly paired with the 5' end of the other strand
B) since the double helix twists, it is not perfectly parallel
C) one strand has a negative charge, and the other strand has a positive charge
D) the 5' end of one strand is directly paired with the 3' end of the other strand
E) both strands have a negative charge
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37
A short RNA chain is synthesized as the first nucleotides in a new DNA strand by the enzyme ____ to provide a ____ for DNA elongation.

A) topoisomerase; 3' hydroxyl group
B) primase; 3' hydroxyl group
C) primase; 5' hydroxyl group
D) DNA polymerase; 5' phosphate group
E) DNA polymerase; 3' hydroxyl group
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38
Which statement correctly describes DNA base pairing?

A) Two hydrogen bonds bind A and T; three hydrogen bonds bind G and C.
B) Two hydrogen bonds bind A and C; three hydrogen bonds bind T and G.
C) Two hydrogen bonds bind G and C; three hydrogen bonds bind A and T.
D) Two hydrogen bonds bind A and T, and two hydrogen bonds bind G and C.
E) Three hydrogen bonds bind A and C, and three hydrogen bonds bind T and G.
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39
In DNA, the purines are ____.

A) thymine and cytosine
B) adenine and cytosine
C) adenine and guanine
D) thymine and adenine
E) guanine and thymine
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40
Wilkins and Franklin studied the structure of DNA using ____.

A) molecular scale models of nucleotides
B) X-ray diffraction
C) computer-assisted graphics
D) electron microscopy
E) light microscopy
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41
During DNA replication, nucleosomes must ____ ahead of the replication fork and ____ after DNA is replicated.

A) disassemble; reassemble
B) reassemble; disassemble
C) unwind DNA; disassociate
D) synthesize primers; proofread
E) cut DNA; ligate DNA
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42
In humans, telomerase ____.

A) adds telomere repeats in some human cells
B) removes telomere repeats in all human cells
C) adds telomere repeats in all human cells
D) removes telomere repeats in some human cells
E) transcribes telomere repeats in some human cells
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43
During normal DNA replication, part of the sequence at the ends of linear chromosomes is not copied into the new DNA strands because ____.

A) DNA ligase cannot join pieces at the end of a chromosome
B) RNA primers at the beginning of a new strand cannot be replaced with DNA
C) those ends are Okazaki fragments that are lost
D) cells do not need the DNA at the ends of chromosomes
E) the ends of chromosomes are made of protein, not DNA
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44
Reiji Okazaki discovered what are now called "Okazaki fragments" produced during DNA replication. These fragments are ____.

A) short lengths of new DNA on the leading strand
B) RNA primers on the lagging strand
C) RNA primers on both the lagging and leading strand
D) short lengths of new DNA on the lagging strand
E) RNA primers on the leading strand
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45
Proofreading by ____ corrects errors that occur during DNA replication.

A) DNA polymerase
B) primase
C) telomerase
D) DNA ligase
E) helicase
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46
The nucleosome core particle consists of ____.

A) two chromosomes linked together
B) RNA wrapped around an eight-protein histone complex
C) DNA wrapped around an eight-protein histone complex
D) DNA associated with the nuclear envelope
E) DNA replication enzymes associating to form the replisome
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47
Individuals with xeroderma pigmentosum inherit a faulty DNA repair mechanism. As a consequence, ____.

A) they are sterile
B) their cells have no proofreading abilities during DNA replication
C) Okazaki fragments produced during DNA replication cannot be joined
D) they easily develop skin cancer when exposed to sunlight
E) their telomeres are shorter than average
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48
The energy to form the new bonds between nucleotides in a growing DNA strand is provided primarily by ____.

A) unwinding of the DNA double helix
B) hydrolysis of pyrophosphate
C) breaking hydrogen bonds between base pairs
D) DNA helicase
E) forming hydrogen bonds between base pairs
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49
Imagine that a cell contains a genetic mutation in the gene encoding the primase enzyme, rendering it unable to synthesize RNA strands. Assuming that all of the other enzymes directly involved in DNA replication are still functional in these cells, how much of the DNA replication process would you expect to see in these cells?

A) The leading strand would be synthesized, but not the lagging strand.
B) No part of the DNA replication process could occur.
C) The DNA helix would be unwound by helicase, but no new strands will be produced.
D) Both the leading and lagging strand would be synthesized, but pieces of discontinuous strands would not be joined together.
E) DNA replication would still proceed completely since RNA strands are not part of the final product of DNA replication.
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50
Telomeres are found ____.

A) in the middle of chromosomes
B) at replication origins
C) where DNA strands are joined together
D) within genes
E) at the ends of chromosomes
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51
Adding nucleotides onto a growing DNA strand during DNA replication in cells occurs in ____.

A) the 5' ->3' direction for the leading strand and the 3' ->5' direction on the lagging strand
B) either the 5' ->3' direction or the 3' ->5' direction on both strands, depending on where replication begins
C) the 5' ->3' direction only
D) the 3' ->5' direction for the leading strand and the 5' ->3' direction on the lagging strand
E) the 3' ->5' direction only
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52
Nucleosomes are best described as ____.

A) prokaryotic DNA associated with nonhistone proteins
B) eukaryotic DNA associated with histone proteins
C) prokaryotic DNA associated with histone proteins
D) eukaryotic DNA associated with nonhistone proteins
E) associated histone and nonhistone proteins
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53
When DNA is replicated, ____.

A) parental histones are degraded and entirely replaced by new histones
B) DNA is permanently freed from histone binding
C) new histone proteins are also produced
D) new histone proteins are not needed
E) the number of histones that bind to each DNA molecule is halved
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54
In eukaryotes, the DNA molecule that comprises a chromosome is ____ and has ____ replication origin.

A) circular, one
B) circular, more than one
C) linear, more than one
D) linear, one
E) linear, no
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55
The components of nucleosomes is(are) ____.

A) DNA only
B) DNA, RNA, and protein
C) DNA and RNA
D) RNA and protein
E) DNA and protein
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56
Without proofreading, the rate of DNA replication errors in bacteria and eukaryotes is as high as one for every ____ nucleotides assembled.

A) 10 to 100
B) 100,000 to 1,000,000
C) 1,000 to 10,000
D) 10,000,000 to 100,000,000
E) 100,000,000 to 1,000,000,000
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57
After DNA repair enzymes remove an incorrect nucleotide resulting from a replication error, ____ is/are needed to complete the repair.

A) primase, DNA polymerase, and DNA ligase
B) DNA polymerase
C) DNA polymerase and DNA ligase
D) primase and DNA ligase
E) primase and DNA polymerase
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58
In prokaryotes, the DNA molecule that makes up a chromosome is ____ and has ____ replication origin.

A) circular; one
B) circular; more than one
C) linear; more than one
D) linear; one
E) linear; no
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59
Suppose you take a cell from an adult cow and attempt to use it to produce a clone of that cow. If telomerase is not functioning in that cell or in any of the cell's progeny, what would you expect to happen to your clone?

A) The clone will be unable to grow.
B) When the clone matures, it will most likely have cancer.
C) The clone's cells may divide, but after a certain number of generations, cell division will stop.
D) The lack of telomerase should have no effect on the clone.
E) When the clone matures, it will most likely be sterile.
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60
During DNA replication, the ____ strand is assembled in the ____ direction as helix unwinding and is synthesized by ____ replication.

A) leading; opposite; continuous
B) lagging; same; discontinuous
C) leading; same; discontinuous
D) lagging; opposite; continuous
E) leading; same; continuous
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61
Match between columns
Point at which the double helix begins unwinding
leading strand
Point at which the double helix begins unwinding
replication fork
Point at which the double helix begins unwinding
origin of replication
Point at which the double helix begins unwinding
replisome
Point at which the double helix begins unwinding
replication bubble
Point at which the double helix begins unwinding
lagging strand
Point at which the double helix begins unwinding
double helix
The strand synthesized in the opposite direction to the movement of the replication fork
leading strand
The strand synthesized in the opposite direction to the movement of the replication fork
replication fork
The strand synthesized in the opposite direction to the movement of the replication fork
origin of replication
The strand synthesized in the opposite direction to the movement of the replication fork
replisome
The strand synthesized in the opposite direction to the movement of the replication fork
replication bubble
The strand synthesized in the opposite direction to the movement of the replication fork
lagging strand
The strand synthesized in the opposite direction to the movement of the replication fork
double helix
The strand synthesized in the direction the replication fork moves
leading strand
The strand synthesized in the direction the replication fork moves
replication fork
The strand synthesized in the direction the replication fork moves
origin of replication
The strand synthesized in the direction the replication fork moves
replisome
The strand synthesized in the direction the replication fork moves
replication bubble
The strand synthesized in the direction the replication fork moves
lagging strand
The strand synthesized in the direction the replication fork moves
double helix
Forms as a result of two replication forks being produced at the origin of replication
leading strand
Forms as a result of two replication forks being produced at the origin of replication
replication fork
Forms as a result of two replication forks being produced at the origin of replication
origin of replication
Forms as a result of two replication forks being produced at the origin of replication
replisome
Forms as a result of two replication forks being produced at the origin of replication
replication bubble
Forms as a result of two replication forks being produced at the origin of replication
lagging strand
Forms as a result of two replication forks being produced at the origin of replication
double helix
Y-shape produced by the unwinding of the DNA double-helix
leading strand
Y-shape produced by the unwinding of the DNA double-helix
replication fork
Y-shape produced by the unwinding of the DNA double-helix
origin of replication
Y-shape produced by the unwinding of the DNA double-helix
replisome
Y-shape produced by the unwinding of the DNA double-helix
replication bubble
Y-shape produced by the unwinding of the DNA double-helix
lagging strand
Y-shape produced by the unwinding of the DNA double-helix
double helix
The structure of DNA
leading strand
The structure of DNA
replication fork
The structure of DNA
origin of replication
The structure of DNA
replisome
The structure of DNA
replication bubble
The structure of DNA
lagging strand
The structure of DNA
double helix
Complex of DNA replication enzymes
leading strand
Complex of DNA replication enzymes
replication fork
Complex of DNA replication enzymes
origin of replication
Complex of DNA replication enzymes
replisome
Complex of DNA replication enzymes
replication bubble
Complex of DNA replication enzymes
lagging strand
Complex of DNA replication enzymes
double helix
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62
Match between columns
Tethers DNA polymerase to the template DNA
single-stranded binding proteins
Tethers DNA polymerase to the template DNA
DNA polymerase III
Tethers DNA polymerase to the template DNA
DNA ligase
Tethers DNA polymerase to the template DNA
helicase
Tethers DNA polymerase to the template DNA
topoisomerase
Tethers DNA polymerase to the template DNA
sliding clamp
Tethers DNA polymerase to the template DNA
primase
Tethers DNA polymerase to the template DNA
DNA polymerase I
Main enzyme that extends RNA primer by adding DNA nucleotides to it
single-stranded binding proteins
Main enzyme that extends RNA primer by adding DNA nucleotides to it
DNA polymerase III
Main enzyme that extends RNA primer by adding DNA nucleotides to it
DNA ligase
Main enzyme that extends RNA primer by adding DNA nucleotides to it
helicase
Main enzyme that extends RNA primer by adding DNA nucleotides to it
topoisomerase
Main enzyme that extends RNA primer by adding DNA nucleotides to it
sliding clamp
Main enzyme that extends RNA primer by adding DNA nucleotides to it
primase
Main enzyme that extends RNA primer by adding DNA nucleotides to it
DNA polymerase I
Unwinds DNA helix
single-stranded binding proteins
Unwinds DNA helix
DNA polymerase III
Unwinds DNA helix
DNA ligase
Unwinds DNA helix
helicase
Unwinds DNA helix
topoisomerase
Unwinds DNA helix
sliding clamp
Unwinds DNA helix
primase
Unwinds DNA helix
DNA polymerase I
Stabilizes single-stranded DNA
single-stranded binding proteins
Stabilizes single-stranded DNA
DNA polymerase III
Stabilizes single-stranded DNA
DNA ligase
Stabilizes single-stranded DNA
helicase
Stabilizes single-stranded DNA
topoisomerase
Stabilizes single-stranded DNA
sliding clamp
Stabilizes single-stranded DNA
primase
Stabilizes single-stranded DNA
DNA polymerase I
Relieves over-winding of DNA ahead of the replication fork
single-stranded binding proteins
Relieves over-winding of DNA ahead of the replication fork
DNA polymerase III
Relieves over-winding of DNA ahead of the replication fork
DNA ligase
Relieves over-winding of DNA ahead of the replication fork
helicase
Relieves over-winding of DNA ahead of the replication fork
topoisomerase
Relieves over-winding of DNA ahead of the replication fork
sliding clamp
Relieves over-winding of DNA ahead of the replication fork
primase
Relieves over-winding of DNA ahead of the replication fork
DNA polymerase I
Synthesizes short RNA segment to initiate new DNA strand
single-stranded binding proteins
Synthesizes short RNA segment to initiate new DNA strand
DNA polymerase III
Synthesizes short RNA segment to initiate new DNA strand
DNA ligase
Synthesizes short RNA segment to initiate new DNA strand
helicase
Synthesizes short RNA segment to initiate new DNA strand
topoisomerase
Synthesizes short RNA segment to initiate new DNA strand
sliding clamp
Synthesizes short RNA segment to initiate new DNA strand
primase
Synthesizes short RNA segment to initiate new DNA strand
DNA polymerase I
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
single-stranded binding proteins
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
DNA polymerase III
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
DNA ligase
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
helicase
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
topoisomerase
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
sliding clamp
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
primase
Contains 5' ->3' exonuclease activity to remove RNA preceding previous Okazaki fragment and uses its 5' ->3' polymerization activity to replace RNA nucleotides with DNA nucleotides
DNA polymerase I
Seals nicks between adjacent DNA segments
single-stranded binding proteins
Seals nicks between adjacent DNA segments
DNA polymerase III
Seals nicks between adjacent DNA segments
DNA ligase
Seals nicks between adjacent DNA segments
helicase
Seals nicks between adjacent DNA segments
topoisomerase
Seals nicks between adjacent DNA segments
sliding clamp
Seals nicks between adjacent DNA segments
primase
Seals nicks between adjacent DNA segments
DNA polymerase I
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63
Match between columns
Showed that DNA replication in Escherichia coli is semiconservative
Avery, MacLeod, and McCarty
Showed that DNA replication in Escherichia coli is semiconservative
Meselson and Stahl
Showed that DNA replication in Escherichia coli is semiconservative
Griffith
Showed that DNA replication in Escherichia coli is semiconservative
Watson and Crick
Showed that DNA replication in Escherichia coli is semiconservative
Hershey and Chase
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Avery, MacLeod, and McCarty
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Meselson and Stahl
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Griffith
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Watson and Crick
Showed that a transforming principle from heat-killed S strain Streptococcus pneumoniae could be used to make the R strain virulent
Hershey and Chase
Showed that the genetic material of bacteriophage T2 is DNA
Avery, MacLeod, and McCarty
Showed that the genetic material of bacteriophage T2 is DNA
Meselson and Stahl
Showed that the genetic material of bacteriophage T2 is DNA
Griffith
Showed that the genetic material of bacteriophage T2 is DNA
Watson and Crick
Showed that the genetic material of bacteriophage T2 is DNA
Hershey and Chase
Worked out the double helix model for DNA structure
Avery, MacLeod, and McCarty
Worked out the double helix model for DNA structure
Meselson and Stahl
Worked out the double helix model for DNA structure
Griffith
Worked out the double helix model for DNA structure
Watson and Crick
Worked out the double helix model for DNA structure
Hershey and Chase
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Avery, MacLeod, and McCarty
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Meselson and Stahl
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Griffith
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Watson and Crick
Showed that DNA is the transforming principle responsible for transforming nonvirulent Streptococcus pneumoniae into a virulent strain
Hershey and Chase
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64
Match between columns
primase
A
primase
C
primase
E
primase
B
primase
D
DNA polymerase III
A
DNA polymerase III
C
DNA polymerase III
E
DNA polymerase III
B
DNA polymerase III
D
topoisomerase
A
topoisomerase
C
topoisomerase
E
topoisomerase
B
topoisomerase
D
helicase
A
helicase
C
helicase
E
helicase
B
helicase
D
single-stranded binding protein
A
single-stranded binding protein
C
single-stranded binding protein
E
single-stranded binding protein
B
single-stranded binding protein
D
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65
Although Watson and Crick are credited with the discovery of the structure of DNA, they based this discovery on the bench work of many other scientists of the time. Name at least three different pieces of knowledge that Watson and Crick used in their discovery that was based on work from other scientists.
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66
Cancer treatments may specifically target rapidly dividing cells by using drugs or chemicals that ____.

A) promote DNA replication only
B) inhibit DNA repair enzymes only
C) inhibit DNA replication only
D) promote DNA replication or inhibit DNA repair enzymes
E) inhibit DNA replication or DNA repair enzymes
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67
Variability in offspring is largely a result of ____.

A) mutations
B) nucleosomes
C) Okazaki fragments
D) DNA repairs
E) RNA primers
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68
The steps of DNA replication and the enzymes involved are largely conserved amongst bacteria, archaea, and eukaryotes. How can this evolutionary conservation be explained?
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69
Avery, MacLeod, and McCarty showed that DNA was the transforming principle by demonstrating that mice survived when injected with a mixture of dead virulent bacteria and live nonvirulent bacteria that were treated with a DNA degrading enzyme. If RNA was the genetic material, what would have been the effect on the mice? Why?
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70
In many cancers, the cancerous cells have fully active telomerase enzymes. Explain how this might play a role in enabling cancer cells to keep rapidly dividing.
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71
In Hershey and Chase's experiment, why would it not have been suitable to use radioactive nitrogen to label DNA?
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72
Describe what happens to the nucleosome during DNA replication.
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73
Some research has indicated that increased exercise is linked to increased telomere length in renewable tissues, like blood. Assuming that telomerase levels are not increased by exercise, what might explain the increase in telomere length?

A) DNA replication occurred more frequently in individuals who exercised.
B) Cell division occurred more rapidly in individuals who exercised.
C) Telomerase activity was higher in individuals who exercised.
D) Telomerase activity was lower in individuals who exercised.
E) Fewer DNA replication errors occurred in individuals who exercised.
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74
Describe the roles of the following enzymes during DNA replication: ligase, single-stranded binding proteins (SSBs), DNA polymerase III, primase, DNA helicase.
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75
Suppose a DNA replication error is not corrected. After two cell divisions, how many of the four daughter cells contain this mutation (assuming that the mistake was never corrected)?

A) none
B) one
C) two
D) three
E) four
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76
Cancer cells ____.

A) maintain telomerase function
B) have longer telomeres than normal cells
C) eventually die due to shortening chromosomes
D) have circular chromosomes
E) cannot replicate their DNA
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77
What are two main reasons why DNA mutations are so rare?
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78
What is the function of the sliding clamp in DNA replication?

A) unwind DNA ahead of the replication fork
B) anchor DNA polymerase to the template strand
C) remove DNA polymerase from the template strand
D) anchor primase to the template strand
E) bind to single stranded DNA to stabilize it before it is replicated
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79
What is unlikely to happen if the sliding clamp is nonfunctional?

A) The overall rate of DNA synthesis is low.
B) The DNA polymerase and the template strand of DNA are not properly anchored together.
C) The DNA polymerase detaches from the DNA after only a few polymerizations.
D) Many thousands of polymerizations occur before the DNA polymerase detaches.
E) The rate of DNA replication is low.
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