Department of Biological Sciences, Tokyo Metropolitan University, Hachioji, Japan.
Research Center for Genomics and Bioinformatics, Tokyo Metropolitan University, Hachioji, Japan.
Genome Biol Evol. 2018 Aug 1;10(8):1875-1881. doi: 10.1093/gbe/evy148.
Many organisms have a global mechanism for dosage compensation (DC) operating along the entire male X chromosome, which equalizes gene expression on the male X with that on the two Xs in females and/or on autosomes. At the initial stage of sex chromosome evolution, however, gene-by-gene (or localized) DC may also be necessary because the degeneration of Y-linked genes occurs independently at different times. We therefore tested whether the up-regulation of X-linked genes depends on the status of their Y-linked homologs, using the young sex chromosomes, neo-X and neo-Y, in Drosophila miranda. In support of the presence of gene-by-gene DC, the extent of up-regulation in males was indeed higher for neo-X-linked genes with pseudogenized neo-Y-linked homologs than for neo-X-linked genes with functional neo-Y-linked homologs. Further molecular evolutionary analysis also supports the idea that many individual neo-X-linked genes first acquired the potential for up-regulation, which then enabled the pseudogenization of neo-Y-linked homologs, without serious deleterious effects on male fitness.
许多生物都有一种全局的剂量补偿(DC)机制,沿着整个雄性 X 染色体起作用,使雄性 X 上的基因表达与雌性中两个 X 上的基因表达和/或常染色体上的基因表达相等。然而,在性染色体进化的初始阶段,也可能需要逐基因(或局部)的 DC,因为 Y 连锁基因的退化是独立于不同时间发生的。因此,我们使用果蝇 Miranda 中的年轻性染色体 neo-X 和 neo-Y,测试了 X 连锁基因的上调是否取决于其 Y 连锁同源物的状态。支持存在逐基因 DC,具有假基因化 neo-Y 连锁同源物的 neo-X 连锁基因在雄性中的上调程度确实高于具有功能性 neo-Y 连锁同源物的 neo-X 连锁基因。进一步的分子进化分析也支持这样的观点,即许多单个的 neo-X 连锁基因首先获得了上调的潜力,然后使 neo-Y 连锁同源物假基因化,而对雄性的适应度没有严重的有害影响。