The genes encoding the red-and green-color-detecting proteins of the human eye are located next to one another on the X chromosome and probably evolved from a common ancestral pigment gene. The two proteins demonstrate 76 percent homology in their amino acid sequences. A normal-visioned woman with both genes on each of her two X chromosomes has a redcolor-blind son who was shown to have one copy of the greendetecting gene and no copies of the red-detecting gene. Devise an explanation for these observations at the chromosomal level (involving meiosis).

Short Answer

Expert verified
Answer: Unequal crossing over during meiosis in the woman's egg cells could explain a normal-visioned woman having a red-color-blind son. This event can lead to the deletion of the red-detecting gene on one X chromosome, which is inherited by the son, causing his red-color-blindness.

Step by step solution

01

Understand the genetic information provided

The genes encoding the red and green color-detecting proteins are located next to each other on the X chromosome and have 76 percent homology in their amino acid sequences. This means that they are similar genes and might have evolved from a common ancestral pigment gene. The woman has both genes on each of her two X chromosomes and has normal vision.
02

Analyze the son's genetic makeup

The woman's son has one copy of the green-detecting gene and no copies of the red-detecting gene, making him red-color-blind. Since males inherit one X chromosome from their mother and one Y chromosome from their father, it means that the son inherited an X chromosome from his mother that carries one copy of the green-detecting gene and no copies of the red-detecting gene.
03

Investigate the possible chromosomal event during meiosis

A possible explanation for these observations can be a chromosomal event like unequal crossing over during meiosis in the woman's egg cells. Unequal crossing over occurs when homologous chromosomes exchange genetic material in an unequal manner, resulting in the duplication of a region on one chromosome and deletion of that same region on the other chromosome.
04

Explain the cause of red-color-blindness in the son

In our case, it is likely that unequal crossing over happened between the red and green genes on the X chromosomes in the woman. This event led to the deletion of the red-detecting gene on one X chromosome, which was inherited by the son, and a possible duplication of the green-detecting gene on the other X chromosome, which was not inherited by the son. As a result, the son lacks the red-detecting gene, causing his red-color-blindness.

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!

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

What is a Barr body, and where is it found in a cell?

Review the Chapter Concepts list on p. \(83 .\) These all center on sex determination or the expression of genes encoded on sex chromosomes. Write a short essay that discusses sex chromosomes as they contrast with autosomes.

In this chapter, we have 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, you should answer the following fundamental questions: (a) How do we know that in humans the X chromosomes play no role in sex determination, while the Y chromosome causes maleness and its absence causes femaleness? (b) How did we originally (in the late 1940 s) analyze the sex ratio at conception in humans, and how has our approach to studying this issue changed in \(2015 ?\) (c) 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? (d) 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?

Describe how nondisjunction in human female gametes can give rise to Klinefelter and Turner syndrome offspring following fertilization by a normal male gamete.

An insect species is discovered in which the heterogametic sex is unknown. An X-linked recessive mutation for reduced wing (rw) is discovered. Contrast the \(F_{1}\) and \(F_{2}\) generations from a cross between a female with reduced wings and a male with normalsized wings when (a) the female is the heterogametic sex. (b) the male is the heterogametic sex.

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