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

Short Answer

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Based on the solution above: A Barr body is an inactive X chromosome in the nucleus of a female cell, which ensures that females express a similar amount of X-linked genes compared to males. The process of inactivation is called X-chromosome inactivation or lyonization. The Barr body is located within the nucleus of a cell and is generally found at the periphery of the nucleus, near the nuclear envelope, as it remains condensed and is not involved in active transcription of genes.

Step by step solution

01

Define Barr body

A Barr body is an inactive X chromosome in the nucleus of a female cell. It was named after Murray Barr, a Canadian scientist who discovered it in 1949. Barr bodies are formed when one of the two X chromosomes in each female cell condenses and becomes inactive. This process of inactivation is called X-chromosome inactivation or lyonization, and it ensures that females express a similar amount of X-linked genes compared to males, who have only one X chromosome.
02

Location of Barr body in a cell

The Barr body is located within the nucleus of a cell. The nucleus is a double-membrane-bound organelle that contains the cell's genetic material (DNA). Since the Barr body is an inactive X chromosome, it is generally found at the periphery of the nucleus, near the nuclear envelope, as it remains condensed and is not involved in active transcription of genes.

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Most popular questions from this chapter

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?

In this chapter, we have focused on sex differentiation, sex chro- mosomes, 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?

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

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?

How do mammals, including humans, solve the "dosage prob- lem" caused by the presence of an \(\mathrm{X}\) and \(\mathrm{Y}\) chromosome in one sex and two X chromosomes in the other sex?

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