Drews U
Anatomisches Institut der Universität Tübingen, Germany.
Cytogenet Cell Genet. 1998;80(1-4):68-74. doi: 10.1159/000014959.
Sex reversed mice are XX males carrying on one of their X chromosomes a translocation of the sex determining region of the Y (Cattanach's Sxr factor). The phenotype corresponds to the Klinefelter syndrome in man. The X linked Tfm (testicular feminization) mutation in the mouse is a frame shift in the androgen receptor gene leading to complete androgen insensitivity. Due to random X inactivation, sex reversed mice heterozygous for Tfm, are mosaics composed of a variable proportion of androgen insensitive X Tfm and androgen sensitive X+ wildtype cells. In the intersexual genital tract, Tfm cells are maintained as undifferentiated cells in the epididymal duct. To the distorted prostate lobes and bulbourethral glands they contribute some lobules of indifferent urethral glands. A large contribution of Tfm cells allows downgrowth of Wolffian and Müllerian ducts to form a vagina. In the external genitalia the stimulatory effect of testosterone is reduced leading to various degrees of feminization correlating with the proportion of Tfm cells present. In the mosaics effects of testosterone, mediated by local growth factors from the wildtype to the Tfm cells, can be distinguished from direct effects expressed only in the wildtype cells. Mediated effects are embryonic induction and morphogenesis of male organs and postnatal maintenance of organ structure and proliferation. The direct effect is cellular differentiation.
性反转小鼠是XX雄性,其一条X染色体上携带Y染色体性别决定区域的易位(卡塔纳赫的Sxr因子)。其表型与人类的克兰费尔特综合征相对应。小鼠中的X连锁Tfm(睾丸女性化)突变是雄激素受体基因中的移码突变,导致完全雄激素不敏感。由于随机X染色体失活,Tfm杂合的性反转小鼠是由可变比例的雄激素不敏感X Tfm和雄激素敏感X +野生型细胞组成的嵌合体。在两性生殖道中,Tfm细胞在附睾管中保持未分化状态。对于扭曲的前列腺叶和尿道球腺,它们贡献了一些未分化尿道腺的小叶。大量的Tfm细胞可使中肾管和苗勒管向下生长形成阴道。在外部生殖器中,睾酮的刺激作用减弱,导致不同程度的女性化,这与存在的Tfm细胞比例相关。在嵌合体中,睾酮的作用可通过从野生型细胞到Tfm细胞的局部生长因子介导,与仅在野生型细胞中表达的直接作用区分开来。介导的作用包括雄性器官的胚胎诱导和形态发生以及器官结构和增殖的产后维持。直接作用是细胞分化。