Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

A homozygous \(A A B B\) mouse was crossed to a homozygous recessive aabb mouse. The \(\mathrm{F}_{1}\) were backcrossed to a homozygous recessive aabb mouse, and the offspring were analyzed for \(A\) and \(B\). The genetic distance between \(A\) and \(B\) was found to be \(10 \mathrm{cM}(\mathrm{mu})\). If 200 mice were analyzed, deduce the phenotypes observed in the offspring.

Short Answer

Expert verified
Answer: The phenotypes observed in the offspring will include both dominant traits (A-B + a-b) in approximately 180 mice and recombinant traits (Ab + aB) in approximately 20 mice.

Step by step solution

01

Determine the genotype of F1 offspring

In the first cross (AA BB) x (aabb), the offspring will inherit one A allele and one a allele, and one B allele and one b allele. Therefore, the genotype of F1 offspring will be AB Ab aB ab.
02

Calculate recombination frequency

Given that the genetic distance between A and B is 10 cM, this indicates that there is a 10% recombination frequency between these genes. This means that in 10% of the offspring, the alleles A and B will be separated during gamete formation due to crossing over.
03

Identify possible genotypes and calculate probabilities from recombination frequency

The possible genotypes of the offspring are: 1. A-B gametes: 45% (non-recombination) of 50% F1 genotype 2. Ab or aB gametes: 5% recombination frequency × 50% F1 genotype 3. a-b gametes: 45% (non-recombination) of 50% F1 genotype
04

Calculate expected genotype distribution in the offspring from the backcross

In the backcross with a homozygous recessive aabb mouse, the genotype probabilities are: 1. A-B + a-b: (45% × 50%) + (45% × 50%) = 90% 2. Ab + aB: (5% × 50%) + (5% × 50%) = 10%
05

Determine the phenotypes observed in the offspring

From expected genotype distribution, we can estimate the number of offspring with each genotype, out of the 200 mice analyzed: 1. A-B + a-b offspring: 90% × 200 = 180 2. Ab + aB offspring: 10% × 200 = 20 As a result, the phenotypes observed in the offspring will include both dominant traits (A-B + a-b) and recombinant traits (Ab + aB).

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Genetic Distance
Genetic distance is a crucial concept for understanding genetic linkage, measured in centimorgans (cM). It indicates how frequently genes on the same chromosome are separated during the formation of gametes due to crossing over. In this case, the genetic distance between genes A and B is 10 cM. This means these genes are likely to recombine and produce different combinations 10% of the time. When genes are close together on a chromosome, they have a smaller genetic distance, which means they have a lower chance of recombination. Conversely, genes that are farther apart have a higher genetic distance and are more likely to undergo recombination. Understanding genetic distance helps in mapping the location of genes on chromosomes, as well as predicting the inheritance patterns in offspring.
Recombination Frequency
Recombination frequency is the percentage at which genetic recombination occurs between two genes. It is directly related to genetic distance and helps us understand how traits are inherited. Given that the genetic distance between A and B is 10 cM, we can infer a 10% recombination frequency. This means that out of 100 meiosis events, you would expect 10 to yield alleles where recombination has occurred between the two loci.
In terms of the mouse example, when we backcross the F1 generation to a homozygous recessive aabb mouse, this 10% recombination frequency predicts the percentage of offspring that will exhibit a combination of the recombinant alleles (Ab, aB) in contrast to the non-recombinant parental alleles (AB, ab). This helps in quantifying how often these genes will assort independently, thus influencing the phenotypic patterns we observe in the next generation.
Understanding recombination frequency allows geneticists to calculate the likelihood of particular genetic traits being passed on, making it a vital tool in genetic linkage studies.
Phenotype Distribution
Phenotype distribution refers to the observable characteristics in a population, determined by the underlying genotypic combinations. In genetic crossing studies, it's essential to predict how these phenotypes distribute among offspring. For our mouse example, we rely on recombination frequency to calculate expected phenotypic outcomes.
After the backcross with a homozygous recessive aabb mouse, we have two groups of phenotypes based on genotype: those with dominant traits (A-B + a-b) and those with recombinant traits (Ab + aB).
  • Non-recombinant phenotypes (A-B and a-b) will constitute around 90% of the offspring, which is 180 mice, showing the expected parental type traits.
  • Recombinant phenotypes (Ab and aB) will show up in about 10% of the offspring, equating to 20 mice, demonstrating the new combination of traits.
Therefore, phenotype distribution helps in determining the proportion of features in the offspring, reflecting the inheritance patterns decided by genetic distance and recombination frequency.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

A female of genotype \\[ \frac{a}{+}+b^{c} \\] produces 100 meiotic tetrads. Of these, 68 show no crossover events. Of the remaining 32,20 show a crossover between \(a\) and \(b, 10\) show a crossover between \(b\) and \(c,\) and 2 show a double crossover between \(a\) and \(b\) and between \(b\) and \(c .\) Of the 400 gametes produced, how many of each of the 8 different genotypes will be produced? Assuming the order \(a-b-c\) and the allele arrangement previously shown, what is the map distance between these loci?

Phenotypically wild \(\mathrm{F}_{1}\) female Drosophila, whose mothers had light eyes \((l t)\) and fathers had straw \((s t w)\) bristles, produced the following offspring when crossed with homozygous lightstraw males: $$\begin{array}{lc} \text { Phenotype } & \text { Number } \\ \text { light-straw } & 22 \\ \text { wild } & 18 \\ \text { light } & 990 \\ \text { straw } & 970 \\ \text { Total } &{2000} \end{array}$$ 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 physi- cal exchange between chromatids? (d) How do we know that sister chromatids undergo recombination during mitosis? (e) When designed matings cannot be conducted in an organism (for example, in humans), how do we learn that genes are linked, and how do we map them?

Why does more crossing over occur between two distantly linked genes than between two genes that are very close together on the same chromosome?

The gene controlling the Xg blood group alleles \(\left(X g^{+} \text {and } X g^{-}\right)\) and the gene controlling a newly described form of inherited recessive muscle weakness called episodic muscle weakness \((E M W X)\) (Ryan et al., 1999 ) are closely linked on the X chromosome in humans at position \(\mathrm{Xp} 22.3\) (the tip of the short arm \() .\) A male with EMWX who is \(\mathrm{Xg}^{-}\) marries a woman who is \(\mathrm{Xg}^{+}\), and they have eight daughters and one son, all of whom are normal for muscle function, the male being \(\mathrm{Xg}^{+}\) and all the daughters being heterozygous at both the \(E M W X\) and \(X g\) loci. Following is a table that lists three of the daughters with the phenotypes of their husbands and children. (a) Create a pedigree that represents all data stated above and in the following table. (b) For each of the offspring, indicate whether or not a crossover was required to produce the phenotypes that are given.

See all solutions

Recommended explanations on Biology Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free