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

Short Answer

Expert verified
Answer: A Barr body is an inactivated X chromosome present in the nucleus of most female mammalian cells, serving as a mechanism to balance the expression levels of X-linked genes between males and females. It is formed during early development and can be found within the nucleus, typically at the nuclear periphery.

Step by step solution

01

Definition of a Barr Body

A Barr body, also known as a sex chromatin, is an inactivated X chromosome present in the nucleus of most female mammalian cells. It represents a mechanism called X-chromosome inactivation used by female organisms to balance the expression levels of X-linked genes between males and females.
02

Formation of a Barr Body

In female mammals, one of the two X chromosomes is inactivated during early development to prevent the overexpression of X-linked genes. This inactivated X chromosome then condenses and becomes a transcriptionally silent structure called a Barr body. The process of X-chromosome inactivation is random, and each cell inactivates either the maternal or paternal X chromosome. As a result, females are considered "mosaic" because their cells may express genes from either the maternal or paternal X chromosome.
03

Location of a Barr Body in a Cell

In a cell, the Barr body is found within the nucleus, typically at the nuclear periphery. Being a condensed structure, it is tightly associated with the nuclear lamina and heterochromatin regions. This inactivated X chromosome remains in the Barr body state throughout the cell's life, and it is also replicated and passed to daughter cells during cell division.

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Most popular questions from this chapter

The paradigm in vertebrates is that, once sex determination occurs and testes or ovaries are formed, secondary sexual differentiation (male vs. female characteristics) is dependent on male or female hormones that are produced. Recently, D. Zhao and colleagues studied three chickens that were bilateral gynandromorphs, with the right side of the body being clearly female and the left side of the body clearly male [Nature 464 : \(237(2010)] .\) Propose experimental questions that can be investigated using these chickens to test this paradigm. What alternative interpretation contrasts with the paradigm?

When cows have twin calves of unlike sex (fraternal twins), the female twin is usually sterile and has masculinized reproductive organs. This calf is referred to as a freemartin. In cows, twins may share a common placenta and thus fetal circulation. Predict why a freemartin develops.

Indicate the expected number of Barr bodies in interphase cells of individuals with Klinefelter syndrome; Turner syndrome; and karyotypes \(47, \mathrm{XYY}, 47, \mathrm{XXX},\) and \(48, \mathrm{XXXX}\)

What is the role of the enzyme aromatase in sexual differentiation in reptiles?

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 \(S R Y\) 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 \(S R Y\) gene), Craig Smith and colleagues were able to "knock down" expression of \(D M R T 1\) in \(Z Z\) embryos using RNA interference techniques (see Chapter 17 ). 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 \(D M R T 1\) gene plays in chickens in contrast to the role the SRY gene plays in humans?

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