Statistics Department, University of California-Berkeley, California, USA.
Mol Biol Evol. 2013 Apr;30(4):781-7. doi: 10.1093/molbev/mss267. Epub 2012 Dec 4.
Y chromosomes have long been dismissed as "graveyards of genes," but there is still much to be learned from the genetic relics of genes that were once functional on the human Y. We identified human X-linked genes whose gametologs have been pseudogenized or completely lost from the Y chromosome and inferred which evolutionary forces may be acting to retain genes on the Y. Although gene loss appears to be largely correlated with the suppression of recombination, we observe that X-linked genes with functional Y homologs evolve under stronger purifying selection and are expressed at higher levels than X-linked genes with nonfunctional Y homologs. Additionally, we support and expand upon the hypothesis that X inactivation is primarily driven by gene loss on the Y. Using linear discriminant analysis, we show that X-inactivation status can successfully classify 90% of X-linked genes into those with functional or nonfunctional Y homologs.
Y 染色体长期以来一直被视为“基因墓地”,但从曾经在人类 Y 染色体上发挥功能的基因的遗传遗迹中,仍然有很多东西需要学习。我们鉴定了人类 X 连锁基因,其配子体已在 Y 染色体上发生假基因化或完全丢失,并推断哪些进化力量可能作用于保留 Y 染色体上的基因。虽然基因丢失似乎主要与重组抑制相关,但我们观察到具有功能性 Y 同源物的 X 连锁基因受到更强的纯化选择,并且表达水平高于具有非功能性 Y 同源物的 X 连锁基因。此外,我们支持并扩展了 X 失活主要由 Y 上的基因丢失驱动的假说。使用线性判别分析,我们表明 X 失活状态可以成功地将 90%的 X 连锁基因分为具有功能性或非功能性 Y 同源物的基因。