Genetic Analysis: An Integrated Approach (3rd Edition)
Genetic Analysis: An Integrated Approach (3rd Edition)
3rd Edition
ISBN: 9780134605173
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Chapter 4, Problem 22P

Xerodermapigmentosum (XP) is an autosomal recessive condition characterized by moderate to severe sensitivity to ultraviolet (UV) light. Patients develop multiple skin lesions on UV-exposed skin, and skin cancers often develop as a result. XP is caused by deficient repair of DNA damage from UV exposure. a. Many genes are known to be involved in repair of UVinduced DNA damage, and several of these genes are implicated in XP. What genetic phenomenon is illustrated by XP? b. A series of 10 skin-cell lines was grown from different XP patients. Cells from these lines were fused, and the heterokaryons were tested for genetic complementation by assaying their ability to repair DNA damage caused by a moderate amount of UV exposure. In the table below, + indicates that the fusion cell line performs normal DNA damage mutation repair, and - indicates defective DNA repair. Use this information to determine how many DNA-repair genes are mutated in the 10 cell lines, and identify which cell lines share the same mutated genes.

Chapter 4, Problem 22P, Xerodermapigmentosum (XP) is an autosomal recessive condition characterized by moderate to severe

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Genes at loci f, m, and w are linked, but their order is unknown.  The F1 heterozygotes from a cross of FFMMWW x ffmmww are test crossed.  The most frequent phenotypes in the test cross progeny will be FMW and fmw regardless of what the gene order turns out to be.  What classes of testcross progeny (phenotypes) would be least frequent if locus m is in the middle? What classes would be least frequent if locus f is in the middle? What classes would be least frequent if locus w is in the middle?

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