GENE INTERACTIONS IN GONADAL DEVELOPMENT
- 1 March 1999
- journal article
- review article
- Published by Annual Reviews in Annual Review of Physiology
- Vol. 61 (1), 417-433
- https://doi.org/10.1146/annurev.physiol.61.1.417
Abstract
▪ Abstract The acquisition of a sexually dimorphic phenotype is a critical event in mammalian development. Although the maturation of sexual function and reproduction occurs after birth, essentially all of the critical developmental steps take place during embryogenesis. Temporally, these steps can be divided into two different phases: sex determination, the initial event that determines whether the gonads will develop as testes or ovaries; and sexual differentiation, the subsequent events that ultimately produce either the male or the female sexual phenotype. A basic tenet of sexual development in mammals is that genetic sex—determined by the presence or absence of the Y chromosome—directs the embryonic gonads to differentiate into either testes or ovaries. Thereafter, hormones produced by the testes direct the developmental program leading to male sexual differentiation. In the absence of testicular hormones, the pathway of sexual differentiation is female. This chapter reviews the anatomic and cellular changes that constitute sexual differentiation and discusses SRY and other genes, including SF-1, WT1, DAX-1, and SOX9, that play key developmental roles in this process. Dose-dependent interactions among these genes are critical for sex determination and differentiation.Keywords
This publication has 86 references indexed in Scilit:
- The Reticulocalbin Gene Maps to the WAGR Region in Human and to the Small Eye Harwell Deletion in MouseGenomics, 1997
- Structural Characterization of HumanAd4bp (SF-1)GeneBiochemical and Biophysical Research Communications, 1996
- Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21Nature Genetics, 1996
- An RNA recognition motif in Wilms' tumour protein (WT1) revealed by structural modellingNature Genetics, 1996
- Identification of a Putative Steroidogenic Factor-1 Response Element in the DAX-1 PromoterBiochemical and Biophysical Research Communications, 1995
- Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related geneNature, 1994
- Complete and partial XY sex reversal associated with terminal deletion of 10q: Report of 2 cases and literature reviewAmerican Journal of Medical Genetics, 1993
- Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashionHuman Molecular Genetics, 1993
- Male development of chromosomally female mice transgenic for SryNature, 1991
- A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motifNature, 1990