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It is believed that any male-determining genes contained on the Y chromosome in humans are not 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?

Short Answer

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Answer: The potential outcomes include: 1) Male-determining genes transferred to the X chromosome, possibly leading to intersex conditions or ambiguous genitalia; 2) Loss of male-determining genes on the Y chromosome, resulting in individuals who are genetically male but don't develop male characteristics; 3) Decreased fertility due to an increased risk of errors during meiosis, producing non-functional or abnormal sperm cells.

Step by step solution

01

Understand Meiosis and Synapsing#Region

Meiosis is a type of cell division that results in four daughter cells, each with half the number of chromosomes of the parent cell. This process is important for producing sex cells (sperm and egg cells), which contain only one set of chromosomes from each parent. During meiosis, homologous chromosomes pair up and undergo a process called synapsis where they exchange genetic material. This exchange is called crossing over and can lead to genetic diversity. In humans, the male-determining gene, SRY, is located on the Y chromosome, which pairs with the X chromosome during meiosis.
02

Consider the Current Y Chromosome Structure#

In the current scenario, it is believed that important male-determining genes on the Y chromosome are not located in the synapsing region, which is the region that exchanges genetic material with its counterpart (the X chromosome) during meiosis. This situation prevents male-determining genes from being transferred to the X chromosome or being mixed with genes from other regions.
03

Potential Outcomes of Male-Determining Genes in Synapsing Region#

If the male-determining genes were located in the synapsing region of the Y chromosome, they could be exchanged with the corresponding genes on the X chromosome during meiosis. This exchange could result in the following outcomes: 1. Male-determining genes could be transferred to the X chromosome: If this occurred, X chromosomes carrying the male-determining genes could result in individuals with a genetic makeup that contains both male and female-determining genes. This situation could lead to various intersex conditions or ambiguous genitalia. 2. Loss of male-determining genes on the Y chromosome: If male-determining genes were exchanged with non-essential genes on the X chromosome, the Y chromosome might lose these critical genes, resulting in individuals who are genetically male but don't develop male characteristics. 3. Decreased fertility: The exchange of genetic material between the X and Y chromosomes could lead to an increased risk of errors during meiosis, which may decrease fertility rates by producing non-functional or abnormal sperm cells. To sum up, locating male-determining genes in the synapsing region of the Y chromosome could lead to various consequences affecting the development of male characteristics and fertility rates.

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Most popular questions from this chapter

Can the Lyon hypothesis be tested in a human female who is homozygous for one allele of the X-linked G6PD gene? Why, or why not?

A group of scientists developing an XX zygote in vitro are curious to see the impact of certain chemicals on the development of the said organism. They incubate the zygote with the help of testosterone and some transcription factors, which are usually produced by the activity of the Y chromosome. They discover that the zygote develops into a sterile female with masculinized reproductive organs. Explain why this happens.

Distinguish between (a) the concepts of sexual differentiation and sex determination and (b) Protenor and Lygaeus modes of sex determination.

In chickens, a key gene involved in sex determination has recently been identified. Called \(D M R T 1\), it is located on the \(Z\) chromosome and is absent on the W chromosome. Like SRY in humans, it is male determining. Unlike \(S R Y\) in humans, however, female chickens (ZW) have a single copy while males (ZZ) have two copies of the gene. Nevertheless, it is transcribed only in the developing testis. Working in the laboratory of Andrew sinclair (a co-discoverer of the human SRY gene), Craig Smith and colleagues were able to "knock down" expression of \(D M R T 1\) in \(\mathrm{ZZ}\) embryos using RNA interference techniques (see Chapter 15 ). In such cases, the developing gonads look more like ovaries than testes [Nature 461: 267 (2009)]. What conclusions can you draw about the role that the DMRTI gene plays in chickens in contrast to the role the SRY gene plays in humans?

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

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