Goodfellow P N, Camerino G
Department of Genetics, University of Cambridge, Downing Street, Cambridge CB2 3EH, UK.
EXS. 2001(91):57-69.
The DAX-1 gene has been involved in the dosage sensitive sex reversal (DSS) phenotype, a male-to-female sex-reversal syndrome due to the duplication of a small region of human chromosome Xp21. Dax-1 and Sry have been shown to act antagonistically in the mouse system, where increasing expression of the former leads to female development and increasing activity of the latter to male development. Although these data strongly implicate DAX-1 in sex determination, the mouse and human proteins appear to behave differently. Absence of DAX-1 is responsible for adrenal hypoplasia congenita, a human inherited disorder characterized by adrenal insufficiency and hypogonadotropic hypogonadism. Unlike human patients, Dax-1-deficient XY mice have normal levels of corticotropins and adrenal hormones but are sterile. Dax-1-deficient females are fertile. The DAX-1 protein, an unusual member of the nuclear hormone receptor, may act as a transcriptional repressor. It has been shown to both repress transcriptional activators by direct protein-protein interactions and to bind DNA hairpin structures and repress target genes.
DAX-1基因与剂量敏感性性反转(DSS)表型有关,DSS是一种由于人类Xp21染色体小区域重复导致的男性向女性性反转综合征。在小鼠系统中,Dax-1和Sry已被证明具有拮抗作用,其中前者表达增加导致雌性发育,后者活性增加导致雄性发育。尽管这些数据强烈表明DAX-1参与性别决定,但小鼠和人类的蛋白质表现似乎有所不同。DAX-1缺失是先天性肾上腺发育不全的原因,这是一种人类遗传性疾病,其特征为肾上腺功能不全和低促性腺激素性性腺功能减退。与人类患者不同,Dax-1缺陷的XY小鼠促肾上腺皮质激素和肾上腺激素水平正常,但不育。Dax-1缺陷的雌性是可育的。DAX-1蛋白是核激素受体的一个特殊成员,可能作为转录抑制因子发挥作用。已证明它既能通过直接的蛋白质-蛋白质相互作用抑制转录激活因子,又能结合DNA发夹结构并抑制靶基因。