Exam 7: Genes Genomics and Chromosomes
Exam 1: Chemical Foundations42 Questions
Exam 2: Molecular Genetic Techniques50 Questions
Exam 3: Protein Structure and Function51 Questions
Exam 4: Culturing and Visualizing Cells36 Questions
Exam 5: Fundamental Molecular Genetic Mechanisms50 Questions
Exam 6: Bio-membrane Structure37 Questions
Exam 7: Genes Genomics and Chromosomes48 Questions
Exam 8: Transcriptional Control of Gene Expression51 Questions
Exam 9: Post-Transcriptional Gene Control49 Questions
Exam 10: Transmembrane Transport of Ions and Small Molecules44 Questions
Exam 11: Cellular Energetics51 Questions
Exam 12: Moving Proteins Into Membranes and Organelles41 Questions
Exam 13: Vesicular Traffic, Secretion, and Endocytosis39 Questions
Exam 14: Signal Transduction and G-Protein Coupled Receptors45 Questions
Exam 15: Signaling Pathways That Control Gene Activity43 Questions
Exam 16: Cell Organization and Movement I: Microfilaments46 Questions
Exam 17: Cell Organization and Movement II: Microtubules and Intermediate Filaments43 Questions
Exam 18: Regulating the Eukaryotic Cell Cycle41 Questions
Exam 19: Integrating Cells Into Tissues44 Questions
Exam 30: Cell Birth, Lineage, and Death39 Questions
Exam 21: Nerve Cells43 Questions
Exam 22: Immunology42 Questions
Exam 23: Cancer43 Questions
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Why is there a need for a specialized structure at the ends of eukaryotic chromosomes and for the enzyme telomerase?
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Because all known DNA polymerases elongate DNA in the 5´ to 3´ direction,all require a RNA or DNA primer to initiate synthesis.As the replication fork approaches the end of the chromosome,DNA synthesis on the leading strand continues to the end of the chromosome without a problem.However,because the lagging strand is synthesized discontinuously,it cannot be replicated in its entirety.When the RNA primer is removed,a short segment of DNA remains single-stranded with no way to make this region double-stranded.If there were no specialized mechanism for replicating DNA at the ends,then the chromosome would shorten with each round of replication.Telomerase is the enzyme that completes DNA synthesis at the telomeres.
All the following statements are true about a nucleosome except:
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C
Which of the following terms describes when a chromosome is replicated everywhere except the telomeres and centromere,but the daughter chromosomes do not separate?
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B
Histone modifications play integral roles in chromatin condensation and function.Which of the following is NOT considered to be a histone modification?
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Which of the following is an algorithm designed to compare the sequence of a newly identified protein with sequences already stored in the GenBank database?
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Which of the following is a typical feature of prokaryotic genes?
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The chicken lysozyme gene is considered to be a solitary gene because
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All the following steps are performed by the enzyme transposase during transposition of bacterial insertion sequences except
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Open reading frame (ORF)analysis is not effective in identifying genes in higher eukaryotes because of the presence of
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Describe how modification of histone tails can control chromatin condensation.
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To examine the folding and compaction of chromatin during mitosis,you will need to isolate and stain chromosomes at a particular stage using a special spreading preparation technique.For the best analysis,the chromosomes must be at which one of the following stages?
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Which of the following pairs of proteins are considered to be paralogous?
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All the following statements about microsatellite DNA are true except:
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"3C" or chromosome conformation capture methods,used to determine the three-dimensional spatial organization of chromatin within nuclei of interphase cells,rely on a series of steps where the end result is the sequence analysis of purified DNA fragments.Which one of the following presents the correct order of steps you as an investigator need to follow in a 3C method strategy?
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