Graves J A
School of Genetics and Human Variation, La Trobe University, Melbourne, Victoria, Australia.
J Exp Zool. 1998 Aug 1;281(5):472-81.
In mammals, male sex determination, as well as spermatogenesis, is controlled by genes on the Y chromosome. Evolutionary comparisons may be used to detect and test candidate genes for these functions, under the hypothesis that the rapid evolution of the mammalian Y chromosome causes it to contain few genes other than those with a critical function in male reproduction. Comparisons of the gene content of sex chromosomes from the three major groups of extant mammals (placentals, marsupials, and monotremes) show that part of the X chromosome, and a corresponding region of the Y, is shared by all mammals and must be very ancient, but part was added relatively recently. Evolution of the mammalian Y took place in several cycles of addition and attrition, as autosomal regions were added to the pseudoautosomal region of one sex chromosome, recombined onto the other, and degraded on the Y. This explains why most genes and pseudogenes on the Y chromosome have relatives on the X. The gene SRY itself is apparently no exception, being closely related to the highly conserved X-linked gene SOX3. Comparisons of SRY/SOX base sequence and gene location in the three groups of mammals suggest that SRY evolved from SOX3 relatively recently by mutation and loss of all sequences outside the HMG box. It is suggested here that, rather than acting as a transcriptional activator, the SRY gene acts to inhibit its paralogue SOX3, which in turn inhibits an ancient autosomal sex-determining gene SOX9.
在哺乳动物中,雄性性别决定以及精子发生均受Y染色体上的基因控制。基于哺乳动物Y染色体的快速进化使其除了包含对雄性生殖具有关键功能的基因外几乎不含有其他基因这一假设,进化比较可用于检测和测试这些功能的候选基因。对现存三大类哺乳动物(胎盘类、有袋类和单孔类)性染色体基因含量的比较表明,X染色体的一部分以及Y染色体的相应区域为所有哺乳动物所共有,且必定非常古老,但部分区域是相对较新添加的。哺乳动物Y染色体的进化发生在几个添加和损耗的循环中,常染色体区域被添加到一条性染色体的假常染色体区域,重组到另一条性染色体上,并在Y染色体上退化。这就解释了为什么Y染色体上的大多数基因和假基因在X染色体上都有相关基因。基因SRY本身显然也不例外,它与高度保守的X连锁基因SOX3密切相关。对三类哺乳动物中SRY/SOX碱基序列和基因位置的比较表明,SRY是相对较近时期通过HMG框外所有序列的突变和缺失从SOX3进化而来的。本文提出,SRY基因并非作为转录激活因子起作用,而是通过抑制其旁系同源基因SOX3来发挥作用,而SOX3又反过来抑制一个古老的常染色体性别决定基因SOX9。