/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 25 Coat color in cats is determined... [FREE SOLUTION] | 91Ó°ÊÓ

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Coat color in cats is determined by genes at several different loci. At one locus on the X chromosome, one allele \(\left(\mathrm{X}^{+}\right)\) encodes black fur; another allele \(\left(\mathrm{X}^{\circ}\right)\) encodes orange fur. Females can be black \(\left(X^{+} X^{+}\right)\) orange \(\left(\mathrm{X}^{\circ} \mathrm{X}^{\circ}\right),\) or a mixture of orange and black called tortoiseshell \(\left(X^{+} X^{o}\right) .\) Males are either black \(\left(X^{+} Y\right)\) or orange \(\left(X^{o} Y\right) .\) Bill has a female tortoiseshell cat named Patches. One night Patches escapes from Bill's house, spends the night out, and mates with a stray male. Patches later gives birth to the following kittens: one orange male, one black male, two tortoiseshell females, and one orange female. Give the genotypes of Patches, her kittens, and the stray male with which Patches mated.

Short Answer

Expert verified
Patches: \( X^{+} X^{o} \), Kittens: \( X^{o} Y \), \( X^{+} Y \), \( X^{+} X^{o} \) (two times), \( X^{o} X^{o} \). Stray male: \( X^{o} Y \).

Step by step solution

01

Determine Patches' Genotype

Patches is a female tortoiseshell cat, which means her genotype must be heterozygous for the fur color allele on the X chromosome. Thus, her genotype is \( X^{+} X^{o} \).
02

Identify Male Kitten Genotypes

The orange male kitten must have one X chromosome from Patches and a Y chromosome from the father. Since the male is orange, it inherited the \( X^{o} \) chromosome, making its genotype \( X^{o} Y \). The black male kitten must have inherited the \( X^{+} \) chromosome from Patches, making its genotype \( X^{+} Y \).
03

Identify Female Kitten Genotypes

The two tortoiseshell female kittens also have a heterozygous combination just like Patches, as they display both black and orange fur. Their genotype is \( X^{+} X^{o} \). The orange female kitten must have inherited two \( X^{o} \) alleles, one from Patches and one from the father, making her genotype \( X^{o} X^{o} \).
04

Determine the Stray Male's Genotype

The stray male cat must have had an \( X^{o} \) chromosome, as evidenced by the orange female kitten. Thus, the stray male's genotype is \( X^{o} Y \).

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Key Concepts

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

X-linked traits
X-linked traits are genetic characteristics that are determined by genes located on the X chromosome. In mammals, including cats, females have two X chromosomes ( X X ), while males have one X and one Y chromosome ( X Y ). This unique chromosomal setup leads to different patterns of inheritance between males and females, particularly when considering traits linked to the X chromosome.
When analyzing X-linked traits, it’s important to understand that because males have only one X chromosome, they express the color dictated by that X chromosome fully. This is why male cats are never tortoiseshell; they can only be either black or orange, depending on whether they inherit an X^{+} or X^{o} chromosome, respectively. Females, on the other hand, can be a combination of these colors if they inherit one of each allele ( X^{+} X^{o} ), resulting in the tortoiseshell pattern.
Learning about X-linked traits helps us understand not only the basic inheritance patterns in genetics but also offers insights into genetic variations and uniqueness in individuals, particularly in the case of feline coat colors.
Genotype determination
Genotype determination involves identifying the genetic makeup of an organism, which can explain its physical appearance, known as the phenotype. In the exercise, we determine the genotype of the felines involved based on the knowledge of X-linked inheritance patterns.
For Patches, the tortoiseshell cat, her mix of black and orange fur indicates her heterozygous genotype ( X^{+} X^{o} ). Each of her kittens’ genotypes can be traced back by considering the chromosomes they inherited from their parents. The orange male kitten comes from an X^{o} and a Y chromosome, while the black male comes from an X^{+} and a Y chromosome. Through this analysis, we determine that the stray male must have provided the X^{o} chromosome as one parent. Hence, we conclude his genotype to be X^{o} Y .
By investigating and deducing from the known genetic principles, we can logically track how each kitten's genotype results from the fusion of their parents' genetic information.
Feline coat color genetics
Feline coat color genetics is a fascinating field that involves the study of how various genes interact to produce different fur colors and patterns. The primary locus involved in determining a cat’s coat color is found on the X chromosome. For instance, in our case study, two main alleles were involved: X^{+} (black) and X^{o} (orange).
The presence or absence of these alleles leads to the various coat colors we observe. While male cats can only be one color because they only inherit one X chromosome (either X^{+} or X^{o}), female cats have the possibility of being tortoiseshell ( X^{+} X^{o} ) due to having two X chromosomes to express both colors simultaneously. This is a simple example of how intricate and specialized feline coat color genetics can be, influenced by only a few genes yet leading to a wide variety of phenotypic expressions.
Understanding these genetic mechanisms is essential, as it provides insights into the inheritance patterns of traits and contributes to the broader field of genetics, helping to unravel the impact of these genes in biodiversity and evolution.

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Most popular questions from this chapter

What is a Barr body? How is it related to the Lyon hypothesis?

Xg is an antigen found on red blood cells. This antigen is caused by an X-linked allele \(\left(X^{a}\right)\) that is dominant over an allele for the absence of the antigen \(\left(\mathrm{X}^{-}\right)\). The inheritance of these X-linked alleles was studied in children with chromosome abnormalities to determine where nondisjunction of the sex chromosomes took place. For each type of mating in parts a through \(d\) indicate whether nondisjunction took place in the mother or in the father and, if possible, whether it took place in meiosis I or meiosis II (assume no crossing over). a. \(X^{a} Y \times X^{-} X^{-} \rightarrow X^{a}\) (Turner syndrome) b. \(X^{a} Y \times X^{a} X^{-} \rightarrow X^{-}\) (Turner syndrome) c. \(X^{a} Y \times X^{-} X^{-} \rightarrow X^{a} X^{-} Y\) (Klinefelter syndrome) d. \(\mathrm{X}^{a} \mathrm{Y} \times \mathrm{X}^{a} \mathrm{X}^{-} \rightarrow \mathrm{X}^{-} \mathrm{X}^{-} \mathrm{Y}\) (Klinefelter syndrome)

Identical twins (also called monozygotic twins) are derived from a single egg fertilized by a single sperm, creating a zygote that later divides into two (see Chapter 6 ). Because identical twins originate from a single zygote, they are genetically identical. Caroline Loat and her colleagues examined nine measures of social, behavioral, and cognitive ability in 1000 pairs of identical male twins and 1000 pairs of identical female twins (C. S. Loat, et al. 2004. Twin Research \(7: 54-61\) ). They found that, for three of the measures (prosocial behavior, peer problems, and verbal ability), the two male twins of a pair tended to be more alike in their scores than were two female twins of a pair. Propose a possible explanation for this observation. What might this observation indicate about the location of genes that influence prosocial behavior, peer problems, and verbal ability?

How does sex determination in Drosophila differ from sex determination in humans?

A woman with normal chromosomes mates with a man who also has normal chromosomes. a. Suppose that, in the course of oogenesis, the woman's sex chromosomes undergo nondisjunction in meiosis I; the man's chromosomes separate normally. Give all possible combinations of sex chromosomes that this couple's children might inherit and the number of Barr bodies that you would expect to see in each of the cells of each child. b. What chromosome combinations and numbers of Barr bodies would you expect to see if the chromosomes separate normally in oogenesis, but nondisjunction of the sex chromosomes takes place in meiosis I of spermatogenesis?

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