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原发性性别决定:遗传学与生物化学

Primary sex determination: genetics and biochemistry.

作者信息

Hall J L, Wachtel S S

出版信息

Mol Cell Biochem. 1980 Dec 10;33(1-2):49-66. doi: 10.1007/BF00224571.

Abstract

On the basis of widespread phylogenetic conservatism, it has been proposed that serologically-defined H-Y antigen is the inducer of primary sex differentiation in mammals, causing the initially indifferent gonad to become a testis rather than an ovary. The proposal has withstood extensive testing in a variety of biological circumstances: XX males have testes and are H-Y+ and fertile XY females lack testicular tissue and are H-Y-; soluble H-Y antigen induces testicular organogenesis in XX indifferent gonads of the fetal calf in culture; H-Y antibody blocks tubular reaggregation of dispersed XY testicular cells, causing them to organize follicular clusters. There is a gonadal receptor for H-Y antigen: fetal ovarian cells that have been exposed to soluble H-Y (released for example by testicular Sertoli cells) take up the molecule and acquire the H-Y+ phenotype; they absorb H-Y antibody in serological tests. Specific uptake of soluble H-Y does not occur in the extra-gonadal tissues. It may be inferred that H-Y antigen is disseminated during embryogenesis and bound by specific receptors in cells of the primordial gonad, and that reaction of H-Y and its receptor signals a program of testicular differentiation, regardless of karyotype. The several anomalies of primary sexual differentiation manifest in such conditions as the XX male, the XX true hermaphrodite, and the XY female can thus reasonably be viewed as specific errors of synthesis, dissemination, and binding of H-Y antigen. H-Y is secreted by 'Daudi' cells, cultured from a human XY Burkitt lymphoma. The Daudi-secreted moiety is a single hydrophobic protein of 18,000 molecular weight. Early attempts to characterize H-Y secreted by testicular Sertoli cells have yielded two molecules, one of 16,500 MW (corresponding to the Daudi-secreted 18,000 MW protein), and one of 31,000 MW. It remains to be ascertained whether both are in fact H-Y antigens, and if so, whether one is a polymer of the other, or whether each represents the product of genes with discrete testis-determining functions.

摘要

基于广泛的系统发育保守性,有人提出血清学定义的H - Y抗原是哺乳动物原发性性别分化的诱导物,它使最初未分化的性腺发育为睾丸而非卵巢。这一观点在各种生物学情况下都经过了广泛的验证:XX男性有睾丸,H - Y抗原呈阳性且可育;XY女性缺乏睾丸组织,H - Y抗原呈阴性;可溶性H - Y抗原可在体外诱导胎牛XX未分化性腺发生睾丸器官形成;H - Y抗体可阻断分散的XY睾丸细胞的管状重新聚集,使其形成滤泡簇。存在H - Y抗原的性腺受体:暴露于可溶性H - Y(例如由睾丸支持细胞释放)的胎儿卵巢细胞会摄取该分子并获得H - Y抗原阳性表型;它们在血清学检测中能吸收H - Y抗体。性腺外组织不会特异性摄取可溶性H - Y。可以推断,H - Y抗原在胚胎发育过程中扩散,并被原始性腺细胞中的特异性受体结合,并且H - Y与其受体的反应标志着睾丸分化程序,而与核型无关。因此,在XX男性、XX真两性畸形和XY女性等情况下出现的几种原发性性分化异常,可合理地视为H - Y抗原合成、扩散和结合的特定错误。H - Y由从人类XY伯基特淋巴瘤培养的“Daudi”细胞分泌。Daudi细胞分泌的部分是一种分子量为18,000的单一疏水蛋白。早期对睾丸支持细胞分泌的H - Y进行表征的尝试得到了两种分子,一种分子量为16,500(对应于Daudi细胞分泌的18,000分子量蛋白),另一种分子量为31,000。目前尚需确定这两种分子是否实际上都是H - Y抗原,如果是,其中一种是否是另一种的聚合物,或者每种是否代表具有离散睾丸决定功能的基因产物。

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