Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

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.

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!

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.

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

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

In the wasp Bracon hebetor, a form of parthenogenesis (the development of unfertilized eggs into progeny) resulting in haploid organisms is not uncommon. All haploids are males. When off. spring arise from fertilization, females almost invariably result. P. W. Whiting has shown that an X-linked gene with nine multiple alleles \(\left(X_{a}, X_{b},\) etc.) controls sex determination. Any homozygous \right. or hemizygous condition results in males, and any heterozygous condition results in females, If an \(X_{a} / X_{b}\) female mates with an \(X_{a}\) male and lays 50 percent fertilized and 50 percent unfertilized eggs, what proportion of male and female offspring will result?

In mice, the X-linked dominant mutation Testicular feminization (Tfin) eliminates the normal response to the testicular hormone testosterone during sexual differentiation, An XY mouse bearing the \(\mathrm{T}\) for allele on the \(\mathrm{X}\) chromosome develops testes, but no further male differentiation occurs the external genitalia of such an animal are female. From this information, what might you conclude about the role of the Tfim gene product and the \(X\) and Y chromosomes in sex determination and sexual differentiation in mammals? Can you devise an experiment, assuming you can "genetically engineer" the chromosomes of mice, to test and confirm your explanation?

An attached-X female fly, \(\overline{X X} Y\) (see the "Insights and Solutions" box), expresses the recessive X-linked white-eye mutation. It is crossed to a male fly that expresses the X-linked recessive miniature-wing mutation. Determine the outcome of this cross in terms of sex, eye color, and wing size of the offspring.

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).

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