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Ch. 5 - Chromosome Mapping in Eukaryotes
Klug - Concepts of Genetics  12th Edition
Klug12th EditionConcepts of Genetics ISBN: 9780135564776Not the one you use?Change textbook
Chapter 5, Problem 12a

In a series of two-point mapping crosses involving five genes located on chromosome II in Drosophila, the following recombinant (single-crossover) frequencies were observed:
Table showing recombinant frequencies between five genes on chromosome II in Drosophila, with values ranging from 6% to 35%.
Given that the adp gene is near the end of chromosome II (locus 83), construct a map of these genes.

Verified step by step guidance
1
Step 1: Identify the genes involved and their recombination frequencies. The genes are pr, adp, vg, c, and b. The recombination frequencies between each pair are given as percentages, which correspond to map distances in centiMorgans (cM).
Step 2: Since adp is near the end of chromosome II at locus 83, start the map with adp at one end. Use the recombination frequencies involving adp to place the other genes relative to it. For example, adp-b is 35%, adp-c is 8%, and adp-vg is 16%. These distances suggest relative positions of b, c, and vg from adp.
Step 3: Use the smaller recombination frequencies between other gene pairs to order the genes between adp and b. For example, pr-b is 6%, pr-vg is 13%, pr-c is 21%, vg-c is 8%, and vg-b is 19%. These values help to determine the order of pr, vg, and c relative to each other and to adp and b.
Step 4: Construct a linear map by placing genes in an order that best fits the recombination frequencies as distances. Remember that recombination frequencies are additive over short distances, so the sum of distances between adjacent genes should approximate the recombination frequency between the genes at the ends of the segment.
Step 5: Verify the map by checking that the calculated distances between all gene pairs closely match the observed recombination frequencies. Adjust the gene order if necessary to minimize discrepancies.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Genetic Linkage and Recombination Frequency

Genetic linkage refers to genes located close together on the same chromosome that tend to be inherited together. Recombination frequency measures how often crossing over occurs between two genes during meiosis, expressed as a percentage. Lower recombination frequencies indicate closer gene proximity, which is essential for constructing genetic maps.
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Chi Square and Linkage

Two-Point Mapping

Two-point mapping involves calculating recombination frequencies between pairs of genes to estimate their relative distances on a chromosome. By analyzing single crossover events between gene pairs, geneticists can order genes linearly and determine map distances in centimorgans (cM), where 1% recombination equals 1 cM.
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Constructing a Genetic Map Using Recombination Data

Constructing a genetic map requires integrating recombination frequencies from multiple gene pairs to determine gene order and distances. Starting with a known gene position (e.g., adp near the chromosome end), one uses the smallest recombination frequencies to place adjacent genes and sums distances to position others, ensuring consistency across all pairwise data.
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Related Practice
Textbook Question

The genes dumpy (dp), clot (cl), and apterous (ap) are linked on chromosome II of Drosophila. In a series of two-point mapping crosses, the following genetic distances were determined. What is the sequence of the three genes?

dp–ap: 42

dp–cl: 3

ap–cl: 39

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Textbook Question

Colored aleurone in the kernels of corn is due to the dominant allele R. The recessive allele r, when homozygous, produces colorless aleurone. The plant color (not the kernel color) is controlled by another gene with two alleles, Y and y. The dominant Y allele results in green color, whereas the homozygous presence of the recessive y allele causes the plant to appear yellow. In a testcross between a plant of unknown genotype and phenotype and a plant that is homozygous recessive for both traits, the following progeny were obtained:

colored, green: 88

colored, yellow: 12

colorless, green: 8

colorless, yellow: 92

Explain how these results were obtained by determining the exact genotype and phenotype of the unknown plant, including the precise arrangement of the alleles on the homologs.

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Textbook Question

In the cross shown here, involving two linked genes, ebony (e) and claret (ca), in Drosophila, where crossing over does not occur in males, offspring were produced in a 2 + : 1 ca : 1 e phenotypic ratio:

These genes are 30 units apart on chromosome III. What did crossing over in the female contribute to these phenotypes?

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Textbook Question

In a series of two-point mapping crosses involving five genes located on chromosome II in Drosophila, the following recombinant (single-crossover) frequencies were observed:

In another set of experiments, a sixth gene, d, was tested against b and pr:

Predict the results of two-point mapping between d and c, d and vg, and d and adp.

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Textbook Question

Two different female Drosophila were isolated, each heterozygous for the autosomally linked genes b (black body), d (dachs tarsus), and c (curved wings). These genes are in the order d–b–c, with b being closer to d than to c. Shown here is the genotypic arrangement for each female along with the various gametes formed by both:

Identify which categories are noncrossovers (NCOs), single crossovers (SCOs), and double crossovers (DCOs) in each case. Then, indicate the relative frequency in which each will be produced.

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Textbook Question

In Drosophila, a cross was made between females—all expressing the three X-linked recessive traits scute bristles (sc), sable body (s), and vermilion eyes (v)—and wild-type males. In the F1, all females were wild type, while all males expressed all three mutant traits. The cross was carried to the F2 generation, and 1000 offspring were counted, with the results shown in the following table.

No determination of sex was made in the data.

Using proper nomenclature, determine the genotypes of the P1 and F1 parents.

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