Mammalian sex determination is controlled by the Y-linked gene SRY. Studies of sex-reversed patients and experimental data obtained with mice have identified other genes, such as DAX1, SOX9, SF1, and WT1, which take part in the process, and have suggested how these genes interact to determine the se
Genetics of mammalian sex determination: Some unloved exceptions
โ Scribed by Mittwoch, Ursula
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 87 KB
- Volume
- 290
- Category
- Article
- ISSN
- 0022-104X
- DOI
- 10.1002/jez.1091
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
The genetics of sex determination is a child of the twentieth century, which overturned the previously held view that sex was determined by the environment. The last quarter of the century witnessed an active search for sexโdetermining genes in mammals. Although successful, the modus operandi of these genes remained unknown, and the relationship between the sexโdetermining systems of mammals and other vertebrates remained enigmatic. To overcome these problems, scientists in the 21st century should heed William Batesonโs counsel to treasure exceptions, for they point the way to progress. One exception to conventional concepts of sex determination is the bilaterally asymmetrical distribution of ovaries and testes in true hermaphroditism. Ovaries favour the left side in humans and the right side in mice. Observations suggesting that a reversal of asymmetry may occur with increasing organ size may point to a possible explanation. A reevaluation is also required regarding the beginning of sex differentiation, in view of mounting evidence of a sex difference in growth rates of early embryos. Another question to be settled is whether the function of SRY is confined to the fetal gonad. The recent demonstration that Sry induces cell proliferation in the fetal mouse gonad (Schmahl et al., 2000) further emphasizes the importance of differential growth in sex determination and differentiation. It is suggested that SRY represents an additional growthโpromoting gene sequestered by mammals to enable the XY embryo to undergo male sex differentiation in the female hormonal environment of the uterus. An increased awareness of the relationship between growth and gonadal differentiation should lead to a better understanding of sex determination in mammals and an ability to relate the function of sexโdetermining genes to the effects of environmental factors. J. Exp. Zool. 290:484โ489, 2001. ยฉ 2001 WileyโLiss, Inc.
๐ SIMILAR VOLUMES
Dosage requirements for runt in the segmentation of Drosophila embryos. Cell 45, 18 GERGEN, J. P. & WIESCHAUS, E. F. (1985). The localized requirements for a gene affecting segmentation in Drosophila: analysis of larvae mosaic for runt. Devl. Biol. 19 GERGEN, J. P. & WIESCHAUS, E. F. (1986). Localiz
In mammals, male sex determination, as well as spermatogenesis, is controlled by genes on the Y chromosome. Evolutionary comparisons may be used to detect and test candidate genes for these functions, under the hypothesis that the rapid evolution of the mammalian Y chromosome causes it to contain fe
## Abstract Pulse pressure (PP) is an independent risk factor for cardiovascular disease. PP rises with age, more so in women. We examined sex differences in the correlations and variance components of PP in adult subjects from 767 nuclear families, enriched with those containing twins, from the Vi
A hypothesis on the evolutionary origin of the genetic pathway of sex determination in the nematode Caenorhabditis elegans is presented here. It is suggested that the pathway arose in steps, driven by frequency-dependent selection for the minority sex at each step, and involving the sequential acqui