SRY: Difference between revisions
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* Humans with one Y chromosome and multiple [[X chromosome]]s ([[Klinefelter's syndrome|XXY]], XXXY etc.) are usually males. |
* Humans with one Y chromosome and multiple [[X chromosome]]s ([[Klinefelter's syndrome|XXY]], XXXY etc.) are usually males. |
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* Individuals with a male [[phenotype]] and an XX (female) [[genotype]] have been observed; these males have the SRY gene in one or both X chromosomes, moved there by [[chromosomal translocation]]. (However, these males are infertile.) |
* Individuals with a male [[phenotype]] and an XX (female) [[genotype]] have been observed; these males have the SRY gene in one or both X chromosomes, moved there by [[chromosomal translocation]]. (However, these males are infertile.) |
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* Similarly, there are females with an XXY or XY genotype. These females have no SRY gene in their Y chromosome, or the SRY gene exists but is defective (mutated). |
* Similarly, there are females with an XXY or XY genotype. These females have no SRY gene in their Y chromosome, or the SRY gene exists but is defective (mutated).<ref>http://www.newscientist.com/article/dn16934</ref> |
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==SRY and the Olympics== |
==SRY and the Olympics== |
Revision as of 17:42, 10 April 2009
This article needs attention from an expert in Genetics. Please add a reason or a talk parameter to this template to explain the issue with the article.(November 2008) |
Template:PBB SRY (Sex-determining Region Y) is a sex-determining gene on the Y chromosome in the therians (placental mammals and marsupials).[1]
This intronless gene encodes a transcription factor that is a member of the high mobility group (HMG)-box family of DNA-binding proteins. This protein is the testis determining factor (TDF), also referred to as the SRY protein, which initiates male sex determination. Mutations in this gene give rise to XY females with gonadal dysgenesis (Swyer syndrome); translocation of part of the Y chromosome containing this gene to the X chromosome causes XX male syndrome.[2]
Effect upon anatomical sex
Since its discovery, the importance of the SRY gene in sex determination has been extensively documented:
- Humans with one Y chromosome and multiple X chromosomes (XXY, XXXY etc.) are usually males.
- Individuals with a male phenotype and an XX (female) genotype have been observed; these males have the SRY gene in one or both X chromosomes, moved there by chromosomal translocation. (However, these males are infertile.)
- Similarly, there are females with an XXY or XY genotype. These females have no SRY gene in their Y chromosome, or the SRY gene exists but is defective (mutated).[3]
SRY and the Olympics
One of the most controversial uses of this discovery was as a means for gender verification at the Olympic Games, under a system implemented by the International Olympic Committee in 1992. Athletes with a SRY gene were not permitted to participate as females, although all athletes in whom this was "detected" at the 1996 Summer Olympics were ruled false positives and were not disqualified. In the late 1990s, a number of relevant professional societies in United States called for elimination of gender verification, including the American Medical Association, the American Academy of Pediatrics, the American College of Physicians, the American College of Obstetricians and Gynecologists, the Endocrine Society and the American Society of Human Genetics, stating that the method used was uncertain and ineffective.[4] The screening was eliminated as of the 2000 Summer Olympics.[4][5][6]
SRY-related diseases and defects
Individuals with XY genotype and functional SRY gene can have a female phenotype, where the underlying cause is androgen insensitivity syndrome (AIS). SRY is essential for 'maleness', loss of SRY gene from Y chromosome means XY individuals that are normally male will have female characteristics (Swyer syndrome).
SRY has been linked to the fact that men are more likely than women to develop dopamine-related diseases such as schizophrenia and Parkinson's disease. SRY makes a protein that controls concentrations of dopamine, the neurotransmitter that carries signals from the brain that control movement and coordination.[7][8]
See also
References
- ^ Wallis MC, Waters PD, Graves JA (2008). "Sex determination in mammals - Before and after the evolution of SRY". Cell. Mol. Life Sci. doi:10.1007/s00018-008-8109-z. PMID 18581056.
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ignored (help)CS1 maint: multiple names: authors list (link) - ^ "Entrez Gene: SRY sex determining region Y".
- ^ http://www.newscientist.com/article/dn16934
- ^ a b Facius, Georg M. (2004). "The Major Medical Blunder of the 20th Century". Bodies Like Ours. Retrieved May 30.
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ignored (help) - ^ Elsas, LJ (2000). "Gender verification of female athletes". Genetics in Medicine. 2 (4): 249–54. doi:10.1097/00125817-200007000-00008. PMID 11252710.
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ignored (help) - ^ Dickinson, BD (2002). "Gender verification of female Olympic athletes". Medicine & Science in Sports & Exercise. 34 (10): 1543. doi:10.1097/00005768-200210000-00002. PMID 12370551.
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ignored (help) - ^ Dewing, P (2006). "Direct regulation of adult brain function by the male-specific factor SRY". Current Biology. 16 (4): 415–20. doi:10.1016/j.cub.2006.01.017. PMID 16488877.
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ignored (help) - ^ Haaxma CA, Bloem BR, Borm GF, Oyen WJ, Leenders KL, Eshuis S, Booij J, Dluzen DE, Horstink MW (2007). "Gender differences in Parkinson's disease". J. Neurol. Neurosurg. Psychiatr. 78 (8): 819–24. doi:10.1136/jnnp.2006.103788. PMID 17098842.
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Further reading
External links
- Genes,+sry at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- Sex-Determining+Region+Y+Protein at the U.S. National Library of Medicine Medical Subject Headings (MeSH)