Sex determination and the control of Sox9 expression in mammals

被引:92
作者
Jakob, Susanne [1 ]
Lovell-Badge, Robin [1 ]
机构
[1] Natl Inst Med Res, MRC, Div Stem Cell Biol & Dev Genet, London NW7 1AA, England
基金
英国医学研究理事会;
关键词
beta-catenin; Fgf9; Foxl2; gene regulatory network; gonad sex reversal; sex determination; Sf1; Sry; TESCO; transdifferentiation; GONADAL DEVELOPMENT; BETA-CATENIN; STEROIDOGENIC FACTOR-1; TESTIS DEVELOPMENT; SERTOLI-CELLS; SRY ACTION; DIFFERENTIATION; REVERSAL; MICE; IDENTIFICATION;
D O I
10.1111/j.1742-4658.2011.08029.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
In mouse sex determination, the presence or absence of Sertoli cells in the developing gonad is essential for the decision to form either a testis or an ovary. The transcription factor SOX9 has emerged as the master regulator of Sertoli cell differentiation during testis development and thus the crucial gene to determine sex. It is the target of two sets of regulatory controls, one positive and one negative, where one set tries to gain dominance over the other in the early gonad and then to establish and maintain the activity or silence of Sox9 throughout life. The data reveal the importance of the positive regulatory loops to reinforce initial decisions, whereas the maintenance of the gonadal phenotype appears to rely on the active repression of the opposite pathway.
引用
收藏
页码:1002 / 1009
页数:8
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