Pask A, Renfree M B, Marshall Graves J A
Department of Genetics and Evolution, La Trobe University, Melbourne 3083, Australia.
Proc Natl Acad Sci U S A. 2000 Nov 21;97(24):13198-202. doi: 10.1073/pnas.230424497.
Mutations in the ATRX gene on the human X chromosome cause X-linked alpha-thalassemia and mental retardation. XY patients with deletions or mutations in this gene display varying degrees of sex reversal, implicating ATRX in the development of the human testis. To explore further the role of ATRX in mammalian sex differentiation, the homologous gene was cloned and characterized in a marsupial. Surprisingly, active homologues of ATRX were detected on the marsupial Y as well as the X chromosome. The Y-borne copy (ATRY) displays testis-specific expression. This, as well as the sex reversal of ATRX patients, suggests that ATRY is involved in testis development in marsupials and may represent an ancestral testis-determining mechanism that predated the evolution of SRY as the primary mammalian male sex-determining gene. There is no evidence for a Y-borne ATRX homologue in mouse or human, implying that this gene has been lost in eutherians and its role supplanted by the evolution of SRY from SOX3 as the dominant determiner of male differentiation.
人类X染色体上的ATRX基因突变会导致X连锁的α地中海贫血和智力发育迟缓。该基因发生缺失或突变的XY患者表现出不同程度的性反转,这表明ATRX在人类睾丸发育中发挥作用。为了进一步探究ATRX在哺乳动物性别分化中的作用,研究人员在有袋类动物中克隆并鉴定了该同源基因。令人惊讶的是,在有袋类动物的Y染色体以及X染色体上都检测到了活跃的ATRX同源物。Y染色体携带的拷贝(ATRY)表现出睾丸特异性表达。这一点以及ATRX患者的性反转表明,ATRY参与有袋类动物的睾丸发育,可能代表了一种先于SRY作为主要哺乳动物雄性性别决定基因进化的祖先睾丸决定机制。在小鼠或人类中没有Y染色体携带的ATRX同源物的证据,这意味着该基因在真兽类中已经丢失,其作用被从SOX3进化而来的SRY作为雄性分化的主要决定因素所取代。