Exam 14: Molecular Genetic Analysis and Biotechnology
Exam 1: Introduction to Genetics69 Questions
Exam 2: Chromosomes and Cellular Reproduction70 Questions
Exam 3: Basic Principles of Heredity65 Questions
Exam 4: Sex Determination and Sex-Linked Characteristics131 Questions
Exam 5: Linkage, Recombination, and Eukaryotic Gene Mapping60 Questions
Exam 6: Chromosome Variation49 Questions
Exam 7: Bacterial and Viral Genetic Systems57 Questions
Exam 8: DNA- the Chemical Nature of the Gene87 Questions
Exam 9: DNA Replication and Recombination59 Questions
Exam 10: From DNA to Proteins- Transcription and Rna Processing50 Questions
Exam 11: From DNA to Protein- Translation58 Questions
Exam 12: Control of Gene Expression89 Questions
Exam 13: Gene Mutations, Transposable Elements, and Dna Repair76 Questions
Exam 14: Molecular Genetic Analysis and Biotechnology69 Questions
Exam 15: Genomics and Proteomics50 Questions
Exam 16: Cancer Genetics60 Questions
Exam 17: Quantitative Genetics56 Questions
Exam 18: Population and Evolutionary Genetics58 Questions
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Explain what an RFLP is.Why do RFLPs behave like "codominant" markers?
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(1)RFLPs (restriction fragment length polymorphisms)are molecular markers that are detected by virtue of the differences in their DNA sequence length. (2)RFLPs are DNA sequences, and thus their detection is not dependent on the expression of a protein or RNA product.Unless the entire region that hybridizes to a probe has been deleted (highly unlikely), all genome copies (e.g., two in a diploid)of an organism will contain some sequences that will anneal to the probe and be detected.At the genomic DNA level, there is no recessiveness or dominance because the DNA itself, rather than a gene product, is being detected by the probe.
You are given a plasmid containing a part of a gene of Drosophila melanogaster.The gene fragment is 303 base-pairs long.You would like to amplify it using PCR.You design oligonucleotide primers 19 nucleotides in length that are complementary to the plasmid sequences immediately adjacent to both ends of the cloning site.What would be the exact length of most of the resulting PCR product in base pairs?
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Correct Answer:
C
Which of the following is a TRUE statement?
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Correct Answer:
D
Which of the following is NOT usually used as a cloning vector in bacteria?
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The genome of Mycobacterium tuberculosis consists of a single circular chromosome that is 4, 410, 000 nucleotides in length and has a 66% (2/3)GC content.The MseI restriction enzyme cuts at a 5' TTAA 3' sequence (one DNA strand given).How many MseI sites should be present in this genome?
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What is the function of dideoxynucleotides in Sanger DNA sequencing?
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Arabidopsis thaliana has one of the smallest genomes among higher plants with a haploid genome size of about 100 million base pairs.If this genome is completely digested with the restriction enzyme NotI that has an eight-base recognition sequence, approximately how many DNA fragments per genome will be produced?
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A cDNA encoding a protein that is specific for a particular strain (strain Q)of bacteria has been cloned.How would you determine whether an infection contains this particular bacterial strain?
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The Federal Bureau of Investigation has developed the Combined DNA Index System (CODIS), which is 13 loci that are used to develop DNA fingerprints for crime solving.Which of the following characteristics is FALSE concerning these 13 loci?
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A geneticist wishes to study the genetic basis of proline biosynthesis in yeast.She first collects as many spontaneous and induced mutations that results, as much as possible, in the inability to synthesize proline.She then investigates the molecular basis for this inability in these mutants.What type of genetic analysis is the geneticist doing?
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mRNA can be transferred from a gel to a solid support and then a probe can be utilized to determine the size and relative abundance of this mRNA.This procedure is called:
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Which of the following is NOT a potential benefit of using transgenic plants?
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Antibodies are to Western blots as _____ are to Southern blots.
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Which of the following is NOT correct regarding the restriction enzymes that are used in biotechnology?
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In using a cloning vector with a multiple cloning site spliced into the front part of the lacZ gene, production of beta-galactosidase, as shown by the blue color when grown on Xgal, indicates that:
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Which of the following is NOT a challenge of working at the molecular level?
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What is the process by which MOST plasmid vectors carrying a cloned piece of DNA are taken up by host bacteria?
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What is an expression vector, and what characteristics should it possess?
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