McElreavey K D, Vilain E, Boucekkine C, Vidaud M, Jaubert F, Richaud F, Fellous M
Unité INSERM U276, Université Paris VII, France.
Genomics. 1992 Jul;13(3):838-40. doi: 10.1016/0888-7543(92)90164-n.
Sex determination in humans is mediated through the expression of a testis-determining gene on the Y chromosome. In humans, a candidate gene for the testis-determining factor (TDF) that encodes a protein with a putative DNA-binding motif and has been isolated is termed SRY. Here we describe an XY sex-reversed female with pure gonadal dysgenesis who harbors a de novo nonsense mutation in the SRY open reading frame (SRY-orf). This single-basepair substitution results directly in the formation of a termination codon in the putative SRY DNA-binding motif, presumably leading to a nonfunctional gene product. This brings the number of reported XY sex-reversed females with de novo mutations in the known SRY-orf to three, each occurring in the putative DNA-binding domain. This provides further evidence to support SRY being TDF in humans and also indicates the functional importance of the putative DNA-binding domain of the SRY protein.
人类的性别决定是通过Y染色体上睾丸决定基因的表达来介导的。在人类中,一个编码具有假定DNA结合基序的蛋白质且已被分离出来的睾丸决定因子(TDF)候选基因被称为SRY。在此,我们描述了一名患有单纯性腺发育不全的XY性反转女性,其SRY开放阅读框(SRY-orf)存在一个新生的无义突变。这种单碱基对替换直接导致在假定的SRY DNA结合基序中形成一个终止密码子,推测会产生一个无功能的基因产物。这使得报道的已知SRY-orf中存在新生突变的XY性反转女性数量增至三人,且每个突变都发生在假定的DNA结合域。这为支持SRY是人类的TDF提供了进一步的证据,也表明了SRY蛋白假定DNA结合域的功能重要性。