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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 the inactive X chromosome in a female cell that has been condensed and rendered transcriptionally silent through the process of X-chromosome inactivation. It is located in the periphery of the nucleus in a female somatic cell, close to the nuclear membrane, and appears as a dense, darkly staining structure under the microscope.

Step by step solution

01

Define a Barr body

A Barr body is the inactive X chromosome in a female cell, which has been condensed and rendered transcriptionally silent. This process is also called X-chromosome inactivation, and it is a way to equalize gene dosage between males (with one X and one Y chromosome) and females (with two X chromosomes).
02

Explain the location of Barr body in a cell

A Barr body is usually found in the periphery of the nucleus in a eukaryotic cell, specifically a female somatic cell. It is positioned close to the nuclear membrane and appears as a dense, darkly staining structure under the microscope.

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Key Concepts

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

X-chromosome Inactivation
X-chromosome inactivation is a critical process in female mammals that serves to balance the expression of X-linked genes. This phenomenon ensures that females, who possess two X chromosomes, do not produce twice the amount of X chromosome gene products compared to males, who have only one X chromosome. The core of this process involves the condensation of one of the two X chromosomes in each cell, which then becomes transcriptionally inactive - a Barr body.

During embryonic development, one X chromosome is randomly chosen in each cell to be silenced, leading to a mosaic pattern of gene expression in female organisms. This X inactivation is initiated by the expression of the XIST gene, which produces RNA that coats the future Barr body and leads to its condensation and inactivation.
Gene Dosage Compensation
Gene dosage compensation is the mechanism by which organisms balance the expression of genes between individuals with different numbers of sex chromosomes. For example, in humans, because males have one X and one Y chromosome (XY), and females have two X chromosomes (XX), there needs to be a system in place to ensure that females don't express double the amount of X-linked genes.

The answer lies in the aforementioned X-chromosome inactivation that occurs in females. With one of her two X chromosomes inactive within each cell, a female effectively matches the gene expression levels of a male's single, active X. This is a beautiful example of natural regulatory systems maintaining homeostasis within the body and underscores the intricate control of gene expression at the cellular level.
Eukaryotic Cell Nucleus
The eukaryotic cell nucleus is the command center of the cell, housing the majority of the cell's genetic material in the form of DNA. This DNA is organized into structures called chromosomes, which carry the instructions for building and maintaining the organism. The nucleus is surrounded by a double membrane called the nuclear envelope, which is studded with pores allowing the transport of molecules like RNA and proteins in and out of the nucleus.

Within the nucleus, the Barr body can be found at the periphery, indicating a long-term and generally irreversible form of gene regulation. The presence of the Barr body of a female cell is just one of the many features that highlight the complexity of the nucleus in regulating the life of a cell. Understanding this remarkable structure is fundamental for grasping how cells control the expression of their genes and ultimately how they function.

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Most popular questions from this chapter

The genes encoding the red-and green-color-detecting proteins of the human eye are located next to one another on the \(\mathrm{X}\) 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 present on each of her two \(x\) chromosomes) has a red-color-blind son who was shown to have one copy of the green- detecting gene and no copies of the red-detecting gene. Devise an explanation for these observations at the chromosomal level (involving meiosis).

In reptiles, sex determination was thought to be controlled by sex-chromosome systems or by temperature-dependent sex determination without an inherited component to sex. But as we discussed in section \(7.6,\) in the Australian lizard, Pogona vitticeps, it was recently revealed that sex is determined by both chromosome composition and by the temperature at which eggs are incubated. What effects might climate change have on temperature-dependent sex determination in this species, and how might this impact the sex ratio for this species in subsequent generations?

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?

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 \(\mathrm{F}_{1}\) and \(\mathrm{F}_{2}\) 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.

Review the Chapter Concepts list on p. \(151 .\) These all center around sex determination or the expres- sion of genes encoded on sex chromosomes. Write a short essay that discusses sex chromosomes as they contrast with autosomes.

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