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Three loci, mitochondrial malate dehydrogenase that forms \(a\) and \(b(M D H a, M D H b),\) glucouronidase that forms 1 and \(2(G U S 1\) \(G U S 2\) ), and a histone gene that forms \(+\) and \(-(H+, H-),\) are located on chromosome \(\\# 7\) in humans. Assume that the \(M D H\) locus is at position \(35, G U S\) at position \(45,\) and \(H\) at position 75 A female whose mother was homozygous for \(M D H a, G U S 2,\) and \(H+\) and whose father was homozygous for \(M D H b, G U S 1,\) and \(H-\) produces a sample of 1000 egg cells. Give the genotypes and expected numbers of the various types of cells she would produce. Assume no chromosomal interference.

Short Answer

Expert verified
Answer: 630

Step by step solution

01

Determine the parental genotypes

The mother is homozygous for MDHa, GUS2, and H+, and the father is homozygous for MDHb, GUS1, and H-. Thus, the mother's genotype is (MDHa MDHa, GUS2 GUS2, H+ H+) and the father's genotype is (MDHb MDHb, GUS1 GUS1, H- H-).
02

Calculate recombination frequencies

The recombination frequency is calculated according to the map distance: recombination frequency = map distance / 100. Given the map distances of the loci, we have: - MDH - GUS: (45 - 35) / 100 = 0.1 - GUS - H: (75 - 45) / 100 = 0.3 - MDH - H: (75 - 35) / 100 = 0.4
03

Determine possible gametes

The female can produce four possible gametes based on the recombination frequencies: 1. MDHa GUS2 H+ (no crossover) 2. MDHa GUS2 H- (crossover between GUS and H) 3. MDHa GUS1 H+ (crossover between MDH and GUS) 4. MDHa GUS1 H- (double crossover)
04

Calculate the probabilities of each gamete

Using the recombination frequencies calculated in Step 2, we can now determine the probabilities of each gamete being produced: 1. Probability(MDHa GUS2 H+) = (1 - 0.1)(1 - 0.3) = 0.63 2. Probability(MDHa GUS2 H-) = (1 - 0.1)(0.3) = 0.27 3. Probability(MDHa GUS1 H+) = (0.1)(1 - 0.3) = 0.07 4. Probability(MDHa GUS1 H-) = (0.1)(0.3) = 0.03
05

Calculate the expected number of each type of egg cell

The female produces a total of 1000 egg cells, so we can now calculate the expected number of each type of egg cell based on the probabilities in Step 4: 1. Expected number of MDHa GUS2 H+ cells = 0.63 * 1000 = 630 2. Expected number of MDHa GUS2 H- cells = 0.27 * 1000 = 270 3. Expected number of MDHa GUS1 H+ cells = 0.07 * 1000 = 70 4. Expected number of MDHa GUS1 H- cells = 0.03 * 1000 = 30
06

Final answer:

The female is expected to produce the following types and numbers of egg cells: 1. 630 MDHa GUS2 H+ cells 2. 270 MDHa GUS2 H- cells 3. 70 MDHa GUS1 H+ cells 4. 30 MDHa GUS1 H- cells

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Most popular questions from this chapter

Why is a 50 percent recovery of single-crossover products the upper limit, even when crossing over always occurs between two linked genes?

Phenotypically wild \(\mathrm{F}_{1}\) female Drosophila, whose mothers had light eyes (It) and fathers had straw (stw) bristles, produced the following offspring when crossed with homozygous light-straw males:$$\begin{array}{lc} \text { Phenotype } & \text { Number } \\ \hline \text { light-straw } & 22 \\ \text { wild } & 18 \\ \text { light } & 990 \\ \text { straw } & \frac{970}{2000} \end{array}$$ Compute the map distance between the light and straw loci.

In this chapter, we focused on linkage, chromosomal mapping, and many associated phenomena. In the process, we found many opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter, what answers would you propose to the following fundamental questions? (a) How was it established experimentally that the frequency of recombination (crossing over) between two genes is related to the distance between them along the chromosome? (b) How do we know that specific genes are linked on a single chromosome, in contrast to being located on separate chromosomes? (c) How do we know that crossing over results from a physical exchange between chromatids? (d) How do we know that sister chromatids undergo recombination during mitosis?

Are sister chromatid exchanges effective in producing genetic variability in an individual? in the offspring of individuals?

Explain why restriction fragment length polymorphisms and microsatellites are important landmarks for mapping purposes.

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