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 5, Problem 31P

A genetic study of an early onset form of heart disease identdies 10 families containing members with the condition. No clear dominant or recessive pattern of inheritance is evident, but an analysis of SNP markers for five families’ iletects a strong association with a marker sat chromosome 12 and genetic linkage analysis for the marker produces a lod score of 2.2.

a. What do the association and lad score results suggest about this genetic marker?

b. What next step do you recommend for this genetic analysis?

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A. Look at the pedigree, and DISREGARD individual II-8 for the moment. Is the pattern of inheritance of Unetan syndrome dominant or recessive?  You may assume that the gene is FULLY-PENETRANT in this family.  Please give two specific reasons that support your conclusion.   B. Now, looking at BOTH the pedigree AND at the Southern blot, is this trait autosomal, X-linked, or Y-linked? Please give two specific reasons that support your conclusion. Once again, disregard II-8 for the moment. One of your two reasons must refer specifically to evidence present in the Southern blot.   C. Define the gene alleles associated with Unetan syndrome. Your alleles MUST be consistent with the pattern of inheritance, AND your genetic notation must be consistent with that used throughout the course. Unetan syndrome allele:  ________        Normal allele: ________
The figure below represents a two-generation pedigree representing the inheritance of hereditary deafness (HD), which, has been shown to be autosomal recessive. Below the pedigree (and aligned with each person in each generation) are Southern blot gels for two RFLP loci. The BamH1 RFLP locus has alleles of either 7 kb or 5 kb and the EcoRI RFLP locus gives either a 4 kb or 3 kb EcoRI fragment. a. Determine if HD is linked to either of these markers. b. If linkage is detected between HD and one of the RFLPs, are there any recombinant offspring that you can detect? c. If linkage is detected between HD and one of the RFLPs, what is the approximate map distance between the two? Do you think that this distance will efficiently and effectively allow the RFLP to track the HD gene?
Four homozygous recessive mutant lines of Drosophilamelanogaster (labeled 1 through 4) showed abnormal legcoordination, which made their walking highly erratic.These lines were intercrossed; the phenotypes of the F1flies are shown in the following grid, in which “+” represents wild-type walking and “−” represents abnormalwalking:1 2 3 41 - + + +2 + - - +3 + - - +4 + + + -a. What type of test does this analysis represent?b. How many different genes were mutated in creatingthese four lines?c. Invent wild-type and mutant symbols, and write outfull genotypes for all four lines and for the F1 flies.d. Do these data tell us which genes are linked? If not,how could linkage be tested?e. Do these data tell us the total number of genes takingpart in leg coordination in this animal?

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Genetic Analysis: An Integrated Approach (3rd Edition)

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