Overview of the Respiratory System
Regulation of the Human Genome (IV)
During X-inactivation, most genes on one of the X chromosomes of a female are inactivated in a mechanism that provides dosage compensation to equalize the level of gene expression of most X-linked genes in females to that of males who have only one X chromosome. This process, often called Lyonization, results in the formation of a Barr body, the highly compacted, inactive X chromosome. In the photograph, Barr bodies are shown by arrows. The form of DNA in the inactive X-chromosome is called heterochromatin.
In human females, one X chromosome or the other is inactivated in each cell early in development. As a result, some human female cells have one X chromosome active, while the rest of the cells have the other X chromosome active. Typically, X-inactivation is random, or near random, meaning that roughly half of a female's cells express the genes of one X chromosome and the other half of her cells express genes from the other X chromosome. However, in some females, X-inactivation is not random, but skewed. In cases of nonrandom, or skewed X-inactivation, all or most cells of a female express X-linked genes from a single X chromosome. In reality, nonrandom X-inactivation may be less representative of the process of X-inactivation than of reduced survival of cells with a particular X chromosome inactivated, making it appear that X-inactivation was nonrandom.
In some cases, females who carry X-linked genetic diseases can be affected by those diseases, if X-inactivation is not random. For example, if a structural abnormality disrupts the pattern of X-inactivation, then most or all of a female's cells will express genes from a single X chromosome. If there are genes that are disrupted by the structural abnormality, and those genes cause a disorder, the female can show symptoms of the disorder. For many X-linked disorders, females will show mild to moderate symptoms. This milder manifestation of an X-linked disorder in females may be related, in part, to the fact that most females have, in addition to a large number of cells expressing the abnormal gene, a large number of cells expressing the normal gene. Symptoms remain milder than those seen in affected males who carry no normal copy of the gene because they carry only a single X chromosome.
Some genes on the inactive X chromosome escape inactivation and remain active in females. These genes are believed to be responsible for many traits of normal females. The lack of these genes in females missing all or parts of a second X chromosome, as occurs in many cases of Turner syndrome, are thought to be associated with many of the clinical features of the syndrome.
Keywords: alternative splicing | enhancers | exons | gene regulation | human genome | imprinting | introns | Lyonization | methylation | promoters | silencers | X chromosome | genome
- Jobling, M. A., Hurles, M. E., & Tyler-Smith, C. (2004). Human evolutionary genetics: Origins, peoples & disease. Garland Science, Taylor and Francis Group.
- Lewin, B. (2004). Genes VIII. Pearson Prentice Hall.
- Nussbaum, R. L., McInnes, R. R., & Willard, H. F. (2004). Thompson & Thompson: Genetics in medicine (6th ed.), revised reprint. Saunders, an imprint of Elsevier.
- Carr, S. M. Barr bodies. Laboratory of Dr. Steven M. Carr, Department of Biology, Memorial University of Newfoundland, St. John's NF, Canada. Retrieved 12-18-2006 from http://www.mun.ca/biology/scarr/Barr_Bodies.html
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