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Under what circumstances can a male cat exhibit a tortoise- shell coat pattern?

Short Answer

Expert verified
Answer: A male cat can exhibit a tortoiseshell coat pattern when it has Klinefelter syndrome (XXY chromosomes) and both X chromosomes carry different "O" gene variants (O and o).

Step by step solution

01

Understand the genetics behind coat color in cats

The tortoiseshell coat pattern in cats is caused by the interaction between two alleles (O and o) of the "O" gene located on the X chromosome. When a cat has two X chromosomes with different "O" gene variants, it produces a tortoiseshell pattern. As male cats typically have XY chromosomes, having two X chromosomes, in this case, is unusual.
02

Consider the chromosomal anomaly in male cats

Sometimes, male cats can have a chromosomal anomaly, known as Klinefelter syndrome (XXY), which results in them having an extra X chromosome. In these cases, the male cat will have both an X and a Y chromosome, as well as an extra X chromosome.
03

Determine the occurrence of tortoiseshell pattern in XXY male cats

For a male cat with Klinefelter syndrome to exhibit a tortoiseshell coat pattern, both of his X chromosomes must carry different "O" gene variants - one with the O allele and the other with the o allele. This will result in the expression of both orange and black pigments, creating the characteristic tortoiseshell pattern. In conclusion, a male cat can exhibit a tortoiseshell coat pattern under the circumstance that it has Klinefelter syndrome (XXY chromosomes) and both X chromosomes carry different "O" gene variants (O and o).

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Key Concepts

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

Coat Color Genetics
In cats, the coat color is a fascinating example of genetics at work. The genetics of coat color, particularly in tortoiseshell cats, involves the interaction between specific alleles located on the X chromosome.

Usually, these alleles are part of the "O" gene. This gene has two primary alleles, O and o, that determine the coat color. The O allele leads to an orange pigment, while the o allele results in a non-orange (black or brown) pigment.

Because these alleles are on the X chromosome, females (XX) can have a combination like OO, Oo, or oo. Only the Oo combination produces the tortoiseshell appearance. Males typically have an XY chromosome set; hence, they usually don’t express tortoiseshell colors unless a genetic anomaly occurs.
  • Female Coat Color Combinations:
    • OO: Usually orange
    • Oo: Tortoiseshell
    • oo: Usually black or brown
  • Male Coat Characteristics:
    • Generally orange or not orange, since they typically possess only one X chromosome
Klinefelter Syndrome
Klinefelter syndrome is a condition related to chromosomal variations and affects both humans and animals. In cats, this syndrome results in the presence of an extra X chromosome in male cats, leading to an XXY chromosomal pattern.

Male cats with Klinefelter syndrome have interesting biological changes due to this extra chromosome. Since they have two X chromosomes and one Y chromosome (XXY), they can display traits typically found in females, such as the tortoiseshell coat pattern.
  • Chromosomal Configuration:
    • XXY leads to conditions seen predominantly in females due to dual X chromosomes
  • Physical Traits:
    • Tortoiseshell pattern in affected cats

It’s important to note that Klinefelter syndrome often comes with some health challenges. These cats may have increased medical issues, and they are usually sterile.
Alleles
Alleles are versions of a gene that determine specific traits like coat color in cats. In the context of our example, alleles O and o govern the presence of orange or black pigments.

These alleles exist on the X chromosome, and the combination a cat inherits will dictate its coat color. For females, having two X chromosomes allows a mix of alleles, leading to diverse patterns like tortoiseshell, while males with a single X chromosome do not naturally show this variety unless they have an additional X chromosome as seen in Klinefelter syndrome.
  • Alleles Role in Traits:
    • O allele: Produces an orange coat
    • o allele: Produces a black or brown coat
  • Combinations Affecting Patterns:
    • Oo: Tortoiseshell in females and XXY males

Understanding alleles helps in comprehending how genetic diversity arises in populations and why certain traits are expressed in both common and extraordinary ways.

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Most popular questions from this chapter

It has been suggested that any male-determining genes contained on the \(Y\) chromosome in humans cannot be located in the limited region that synapses with the X chromosome during meiosis. What might be the outcome if such genes were located in this region?

Describe how temperature variation controls sex determination in crocodiles.

In this chapter, we focused on sex differentiation, sex chromosomes, and genetic mechanisms involved in sex determination. At the same time, 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 do we know that specific genes in maize play a role in sexual differentiation? (b) How do we know whether or not a heteromorphic chromosome such as the Y chromosome plays a crucial role in the determination of sex? (c) How do we know that in humans the X chromosomes play no role in human sex determination, while the Y chromosome causes maleness and its absence causes femaleness? (d) How did we learn that, although the sex ratio at birth in humans favors males slightly, the sex ratio at conception favors them much more? (e) How do we know that Drosophila utilizes a different sexdetermination mechanism than mammals, even though it has the same sex-chromosome compositions in males and females? (f) How do we know that X chromosomal inactivation of either the paternal or maternal homolog is a random event during early development in mammalian females?

What does the apparent need for dosage compensation mechanisms suggest about the expression of genetic information in normal diploid individuals?

How does \(X\) chromosome dosage compensation in Drosophila differ from that process in humans?

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