Genetic Analysis: An Integrated Approach (2nd Edition)
Genetic Analysis: An Integrated Approach (2nd Edition)
2nd Edition
ISBN: 9780321948908
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Chapter 6, Problem 26P

Five rII partial-deletion mutants are mapped and then tested for their ability to form wild - type recombinants with six point mutants. The extent and endpoints of deletion mutants are shown below the rII region of the chromosome.

a. Use the data in Table A to place each point mutation as precisely as you can along the chromosome.

Chapter 6, Problem 26P, Five rII partial-deletion mutants are mapped and then tested for their ability to form wild - type , example  1

b. Use the complementation data in Table B to determine where the division between rIIA and rIIB is located on the rII region.

Chapter 6, Problem 26P, Five rII partial-deletion mutants are mapped and then tested for their ability to form wild - type , example  2

c. Based on the data and on your analysis, draw a complementation table for the five point mutants 55, 67, 74, 82, and 85 . (Skip mutant 91 for this problem.)

d. Add mutant 91 to your complementation table (assume it maps to rIIA).

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In each of the illustrations below, a segment of a chromosome has two copies of a transposable element. In panel a, they are oriented in the same direction, whereas in panel b they are in opposite directions. A double strand break occurs in element A and is repaired by homologous recombination using element B as a repair template. For each case, what will the chromosome look like after homologous recombination occurs? Choose one of the five options below, 1-5.
A pair of paralogous repeats, A and B, have 96% sequence similarity and therefore can promote non-allelic homologous recombination (NAHR). They exist in four possible arrangements in a genome, illustrated below as arrangements 1 – 4. What is the result of NAHR between repeats A and B in arrangement 1? A.Translocation between chromosomes 1 and 2 resulting in monocentric chromosomes B.Deletion or duplication of the region between A and B C.Translocation between chromosomes 1 and 2 resulting in acentric and dicentric chromosomes D.Inversion of the region between A and B
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Genetic Analysis: An Integrated Approach (2nd Edition)

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