Deck 16: Gene Regulation in Eukaryotes
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Question
Unlock Deck
Sign up to unlock the cards in this deck!
Unlock Deck
Unlock Deck
1/60
Play
Full screen (f)
Deck 16: Gene Regulation in Eukaryotes
1
Results from RNAi studies are most likely to vary due to
A) varying amount of cellular uptake of dsDNA.
B) its low heritability.
C) different levels of starting mRNA.
D) issues related to fertilization.
E) differences in translation.
A) varying amount of cellular uptake of dsDNA.
B) its low heritability.
C) different levels of starting mRNA.
D) issues related to fertilization.
E) differences in translation.
A
2
What is the most common cause of rare spontaneous ectopic gene expression?
A) insertion mutation
B) deletion mutation
C) a mutation that moves the gene next to a new regulatory element
D) point mutation
E) substitution mutation
A) insertion mutation
B) deletion mutation
C) a mutation that moves the gene next to a new regulatory element
D) point mutation
E) substitution mutation
C
3
What technique is most efficiently used to produce a phenocopy?
A) RNAi
B) transgene
C) isolation of mutations
D) QTL mapping analysis
E) phosphorylation
A) RNAi
B) transgene
C) isolation of mutations
D) QTL mapping analysis
E) phosphorylation
A
4
Which of the following is not a type of loss-of-function mutation?
A) conditional
B) hypomorphic
C) null
D) dominant-negative
E) ectopic
A) conditional
B) hypomorphic
C) null
D) dominant-negative
E) ectopic
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
5
A partial loss-of-function mutation is
A) null.
B) hypomorphic.
C) conditional.
D) dominant-negative.
E) hypermorphic.
A) null.
B) hypomorphic.
C) conditional.
D) dominant-negative.
E) hypermorphic.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
6
What is the most significant advantage of using RNAi to study development?
A) Geneticists have only been able to identify a subset of the genes involved in development.
B) Genetic studies on a single gene can be completed without the creation or isolation of new mutant organisms.
C) RNA is easy to isolate.
D) RNAi causes phenotypes not typical of in vivo development.
E) RNAi always completely silences a single gene.
A) Geneticists have only been able to identify a subset of the genes involved in development.
B) Genetic studies on a single gene can be completed without the creation or isolation of new mutant organisms.
C) RNA is easy to isolate.
D) RNAi causes phenotypes not typical of in vivo development.
E) RNAi always completely silences a single gene.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
7
A ligand secreted from a cell to a nearby cell that signals developmental differentiation is called
A) juxtacrine factor.
B) paracrine factor.
C) endocrine factor.
D) exocrine factor.
E) autonomous factor.
A) juxtacrine factor.
B) paracrine factor.
C) endocrine factor.
D) exocrine factor.
E) autonomous factor.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
8
Mutations that disrupt the earliest stages of human development almost always cause
A) no effect.
B) polydactyly.
C) spontaneous abortion.
D) disruption of the segmented body plan.
E) immunodeficiency.
A) no effect.
B) polydactyly.
C) spontaneous abortion.
D) disruption of the segmented body plan.
E) immunodeficiency.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
9
A loss-of-function mutation that depends on special circumstances is called
A) null.
B) hypomorphic.
C) conditional.
D) dominant-negative.
E) codominant.
A) null.
B) hypomorphic.
C) conditional.
D) dominant-negative.
E) codominant.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
10
Gain-of-function alleles are usually
A) null.
B) conditional.
C) recessive.
D) dominant.
E) hypervariable.
A) null.
B) conditional.
C) recessive.
D) dominant.
E) hypervariable.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
11
What type of mutation is particularly useful to researchers who wish to study a gene's effect on development when a natural loss-of function mutation has not yet been isolated?
A) haploinsufficient
B) hypomorphic
C) conditional
D) dominant-negative
E) recessive
A) haploinsufficient
B) hypomorphic
C) conditional
D) dominant-negative
E) recessive
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
12
Which of the following is not a taboo on the use of humans in genetics studies?
A) phenotypic analysis
B) experimental manipulation of affected individuals
C) forced matings
D) deliberate production of mutants
E) controlled environments
A) phenotypic analysis
B) experimental manipulation of affected individuals
C) forced matings
D) deliberate production of mutants
E) controlled environments
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
13
An unusual loss-of-function mutation that is not recessive is
A) null.
B) hypomorphic.
C) conditional.
D) dominant-negative.
E) epistatic.
A) null.
B) hypomorphic.
C) conditional.
D) dominant-negative.
E) epistatic.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
14
Which of the following is not true of RNAi?
A) it depletes the protein products of genes.
B) it depends on dsRNA to trigger the degradation of mRNA.
C) it can be used to create a functional knock-out.
D) it always produces the same results in replicated experiments.
E) it is used in model organisms.
A) it depletes the protein products of genes.
B) it depends on dsRNA to trigger the degradation of mRNA.
C) it can be used to create a functional knock-out.
D) it always produces the same results in replicated experiments.
E) it is used in model organisms.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
15
Which of the following is most likely to cause a gain-of-function mutation?
A) deletion of a promoter region
B) constitutive activation of an enzyme
C) a synonymous mutation
D) a null mutation
E) RNAi
A) deletion of a promoter region
B) constitutive activation of an enzyme
C) a synonymous mutation
D) a null mutation
E) RNAi
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
16
Mutations that result in a new phenotype for a gene through the production of too much protein are best described by the term
A) conditional.
B) permissive.
C) hypomorphic.
D) gain of function.
E) null.
A) conditional.
B) permissive.
C) hypomorphic.
D) gain of function.
E) null.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
17
Signaling factors that complete cell-to-cell communication in the form of direct contact are called
A) juxtacrine factors.
B) paracrine factors.
C) endocrine factors.
D) exocrine factors.
E) autocrine factors.
A) juxtacrine factors.
B) paracrine factors.
C) endocrine factors.
D) exocrine factors.
E) autocrine factors.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
18
The expression of a gene at an abnormal place or time is called
A) epistasis.
B) ectopic.
C) epigenetic.
D) expressivity.
E) erratic.
A) epistasis.
B) ectopic.
C) epigenetic.
D) expressivity.
E) erratic.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
19
Ligands that circulate throughout the body and signal developmental differentiation are called
A) juxtacrine factors.
B) paracrine factors.
C) endocrine factors.
D) exocrine factors.
E) autonomous factors.
A) juxtacrine factors.
B) paracrine factors.
C) endocrine factors.
D) exocrine factors.
E) autonomous factors.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
20
The Aniridia gene in humans is involved in eye formation.Although eye development is very different in flies,this gene is highly conserved.What is its homolog in Drosophila?
A) eyeless (ey)
B) Pax6
C) noeye (ne)
D) ommatidia (om)
E) Hox9
A) eyeless (ey)
B) Pax6
C) noeye (ne)
D) ommatidia (om)
E) Hox9
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
21
A cloned organism will always be genotypically and phenotypically identical to the individual from which it was cloned.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
22
What technique would you use to best determine when and in what cells of a given tissue a specific gene is expressed?
A) Northern analysis
B) In situ hybridization
C) RT-PCR
D) Southern analysis
E) PCR
A) Northern analysis
B) In situ hybridization
C) RT-PCR
D) Southern analysis
E) PCR
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
23
How would you best follow the developmental timing of a given protein in vivo?
A) in situ hybridization
B) western blotting
C) using a GFP-fusion protein transgenic organism
D) microarray analysis
E) PCR
A) in situ hybridization
B) western blotting
C) using a GFP-fusion protein transgenic organism
D) microarray analysis
E) PCR
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
24
Developmental regulation occurs mostly at the level of mRNA stability.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
25
The presence of a homeodomain in a protein suggests what about its function?
A) It has kinase activity.
B) It is a membrane bound receptor.
C) It is a secreted protein.
D) It is a transcription factor.
E) It has phosphorylase activity.
A) It has kinase activity.
B) It is a membrane bound receptor.
C) It is a secreted protein.
D) It is a transcription factor.
E) It has phosphorylase activity.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
26
Which of the following is a zygotic gap gene in Drosophila?
A) knirps (kni)
B) even-skipped (eve)
C) caudal (cad)
D) hedgehog (hh)
E) agamous (ag)
A) knirps (kni)
B) even-skipped (eve)
C) caudal (cad)
D) hedgehog (hh)
E) agamous (ag)
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
27
A molecule whose concentration determines the developmental fate of a cell is called
A) monomorphic.
B) a juxtacrine protein.
C) a signaling molecule.
D) a morphogen.
E) a paracrine molecule.
A) monomorphic.
B) a juxtacrine protein.
C) a signaling molecule.
D) a morphogen.
E) a paracrine molecule.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
28
In Drosophila,two maternal transcripts that are distributed evenly throughout the oocyte prior to fertilization are:
A) caudal and knirps
B) bicoid and nanos
C) caudal and hunchback
D) agamous and hunchback
E) caudal and agamous
A) caudal and knirps
B) bicoid and nanos
C) caudal and hunchback
D) agamous and hunchback
E) caudal and agamous
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
29
Which of the choices gives the correct sequence of early embryonic development in Drosophila?
A) zygote,syncytial blastoderm,multinucleate syncytium,cellular blastoderm
B) zygote,cellular blastoderm,syncytial blastoderm,multinucleate syncytium
C) zygote,multinucleate syncytium,syncytial blastoderm,cellular blastoderm
D) zygote,syncytial blastoderm,cellular blastoderm,multinucleate syncytium
E) cellular blastoderm,multinucleate syncytium,zygote,syncytial blastoderm
A) zygote,syncytial blastoderm,multinucleate syncytium,cellular blastoderm
B) zygote,cellular blastoderm,syncytial blastoderm,multinucleate syncytium
C) zygote,multinucleate syncytium,syncytial blastoderm,cellular blastoderm
D) zygote,syncytial blastoderm,cellular blastoderm,multinucleate syncytium
E) cellular blastoderm,multinucleate syncytium,zygote,syncytial blastoderm
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
30
In Drosophila embryos,segment polarity genes operate prior to pair-rule genes.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
31
Screening for maternal-effect mutations would involve looking for which of the following?
A) unusual phenotypes in female progeny
B) embryos that are all obviously developmentally arrested
C) asymmetric mutations
D) eggs that can not be fertilized
E) dominant negative phenotypes
A) unusual phenotypes in female progeny
B) embryos that are all obviously developmentally arrested
C) asymmetric mutations
D) eggs that can not be fertilized
E) dominant negative phenotypes
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
32
Maternal and zygotic genes affect early development.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
33
Development requires progressive changes in gene expression.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
34
What does a homeodomain do?
A) acts as a receptor
B) has kinase activity
C) binds to specific DNA sequences
D) causes transposition
E) induces cell division
A) acts as a receptor
B) has kinase activity
C) binds to specific DNA sequences
D) causes transposition
E) induces cell division
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
35
Cells that provide large amounts of mRNA and proteins for deposition into the egg are called
A) doctor cells.
B) nurse cells.
C) helper cells.
D) bicoid cells.
E) pump cells.
A) doctor cells.
B) nurse cells.
C) helper cells.
D) bicoid cells.
E) pump cells.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
36
Bicoid is a maternal-effect mutation that results in larvae with two heads.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
37
Although stem cells can continue dividing indefinitely,half of the cells they give rise to can differentiate into a variety of different cell types.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
38
The green fluorescent protein gene is often joined to genes of interest thus producing a fusion protein that is easily followed in vivo.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
39
An example of ectopic gene expression is shown by
A) achondroplastic dwarfism.
B) lack of eye development.
C) abnormal vulvar shape.
D) legs instead of antennae.
E) stem cells.
A) achondroplastic dwarfism.
B) lack of eye development.
C) abnormal vulvar shape.
D) legs instead of antennae.
E) stem cells.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
40
A nurse cell produces large amounts of mRNA and proteins for deposit into the Drosophila egg.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
41
You recover Drosophila embryos in which,instead of having a head region and tail region,have two tail regions in mirror-image arrangement.Describe a maternal mutation that could cause this condition.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
42
Due to ethical considerations,development is studied in model organisms.How do you use genetic information gained from other species to isolate the human genes involved in development?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
43
The homeodomain is a common DNA-binding domain in many transcription factors that regulate development.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
44
What properties of C.elegans is a transparent round worm with an invariant number of cells in the adult.The female is a hermaphrodite.C.elegans make it the most useful model organism?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
45
How can hypomorphic mutations help "tease" out pleiotropic effects in development?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
46
The maternal Nanos (nos)RNA transcript is the primary anterior morphogen in Drosophila zygote development.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
47
Bicoid is a maternal protein deposited in the anterior region of the egg in Drosophila.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
48
One action of the Bicoid protein is to repress the translation of the caudal (cdl)transcripts.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
49
The sequence of early embryonic development in Drosophila is zygote,multinucleate syncytium,syncytial blastoderm,and cellular blastoderm.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
50
How do cells which all contain identical genetic information differentiate into myriad cell types and ultimately undergo the "miracle" of development from an embryo into a child?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
51
What is the molecular basis of haploinsufficiency?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
52
What gene controls eye development and to what degree is it evolutionarily conserved?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
53
What kind of mutation would be most helpful to test a hypothesis regarding the timing of developmental stages?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
54
What three characteristics of value to geneticists do model organisms share?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
55
You are a very lucky scientist.You observe that an interesting mutant phenotype has arisen in your cell culture.A clonal kidney cell line has what appears to be a patch of muscle cells growing in it.(This suggests that the cell began from a single mutant cell. )You wish to test the hypothesis that gene expression changes result in a change in morphology.How would you test your hypothesis?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
56
Maternal mRNA transcripts of the bicoid (bcd)gene are deposited in the anterior portion of the egg in Drosophila.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
57
What is a dominant-negative mutation?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
58
What advantages,in particular,do yeast cells provide with respect to the study of eukaryotes?
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
59
Model organisms are useful for the study of developmental genetics because significant ethical limitations restrict studies in humans.Discuss some taboos to research in humans.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck
60
Describe the hierarchy of expression of zygotic genes in determining segmentation in Drosophila embryos.
Unlock Deck
Unlock for access to all 60 flashcards in this deck.
Unlock Deck
k this deck