Genetics: From Genes to Genomes
Genetics: From Genes to Genomes
6th Edition
ISBN: 9781259700903
Author: Leland Hartwell Dr., Michael L. Goldberg Professor Dr., Janice Fischer, Leroy Hood Dr.
Publisher: McGraw-Hill Education
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Chapter 20, Problem 13P

Concerning the Tools of Genetics Box Analysis of Cell-Cycle Mutants in Yeast:

a. Describe how you would use replica plating of mutagenized, haploid yeast cells to identify temperature-sensitive (ts) mutations in essential genes needed for yeast growth and survival.
b. Among the many ts mutations you found in part (a), how would you distinguish mutations in genes needed for cell-cycle progression from those in genes needed for other aspects of the life of yeasts?
c. If you had a large collection of yeast cell-cycle mutants, how would you determine which of the mutations are in the same gene and which are in different genes?
d. Figures A and B in the Tools of Genetics Box show a culture of a single yeast ts cell-cycle mutant. The two figures show the same petri plate of cells examined at different times: Fig. A before the shift to restrictive temperature, and Fig. B after the temperature shift. Cells with small buds in Fig. A arrest as a single large budded cell in Fig. B (the yellow arrows point to an example). In contrast, cells with large buds in Fig. A arrest as two large-budded cells in Fig. B (red arrows). What do these observations tell you about when during the cell cycle the protein product of the gene in question normally functions?
e. Describe in detail an experiment to show that the human gene for the cyclin-dependent kinase CDK1 can replace the function of the homologous gene in yeast.
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Describe how you would use replica plating of mutagenized, haploid yeast cells to identify temperature-sensitive (ts) mutations in essential genes needed for yeast growth and survival.
Expression of recombinant proteins in yeast is an important tool for biotechnology companies that produce new drugs for human use. In an attempt to get a new gene X expressed in yeast, a researcher has integrated gene X into the yeast genome near a telomere. Will this strategy result in good expression of gene X? Why or why not? Would the outcome of this experiment differ if the experiment had been performed in a yeast line containing mutations in the H3 or H4 histone tails?
Most organisms display a circadian rhythm, a cycling of biological processes that is roughly synchronized with day length.  In Drosophila, pupae eclose (emerge as adults after metamorphosis) at dawn. a)Using this knowledge how would screen for Drosophila mutants that have an impaired circadian rhythm? b)In each case, how would you clone the genes you identified by mutation?

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Genetics: From Genes to Genomes

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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY