Whittle C A, Sun Y, Johannesson H
Department of Evolutionary Biology, Uppsala University, Uppsala, Sweden.
Eukaryot Cell. 2011 Apr;10(4):594-603. doi: 10.1128/EC.00284-10. Epub 2011 Feb 18.
The origin and early evolution of sex chromosomes are currently poorly understood. The Neurospora tetrasperma mating-type (mat) chromosomes have recently emerged as a model system for the study of early sex chromosome evolution, since they contain a young (<6 million years ago [Mya]), large (>6.6-Mb) region of suppressed recombination. Here we examined preferred-codon usage in 290 genes (121,831 codon positions) in order to test for early signs of genomic degeneration in N. tetrasperma mat chromosomes. We report several key findings about codon usage in the region of recombination suppression, including the following: (i) this region has been subjected to marked and largely independent degeneration among gene alleles; (ii) the level of degeneration is magnified over longer periods of recombination suppression; and (iii) both mat a and mat A chromosomes have been subjected to deterioration. The frequency of shifts from preferred codons to nonpreferred codons is greater for shorter genes than for longer genes, suggesting that short genes play an especially significant role in early sex chromosome evolution. Furthermore, we show that these degenerative changes in codon usage are best explained by altered selection efficiency in the recombinationally suppressed region. These findings demonstrate that the fungus N. tetrasperma provides an effective system for the study of degenerative genomic changes in young regions of recombination suppression in sex-regulating chromosomes.
目前,性染色体的起源和早期演化仍知之甚少。粗糙脉孢菌的四极性交配型(mat)染色体最近成为研究早期性染色体演化的一个模型系统,因为它们包含一个年轻的(<600万年前[Mya])、大片段的(>660万个碱基对)重组抑制区域。在此,我们检测了290个基因(121,831个密码子位点)中最优密码子的使用情况,以测试粗糙脉孢菌mat染色体基因组退化的早期迹象。我们报告了关于重组抑制区域密码子使用的几个关键发现,包括:(i)该区域在基因等位基因间经历了显著且基本独立的退化;(ii)退化程度在更长时间的重组抑制过程中被放大;(iii)mat a和mat A染色体均已发生退化。较短基因从最优密码子转变为非最优密码子的频率高于较长基因,这表明短基因在早期性染色体演化中发挥着尤为重要的作用。此外,我们表明密码子使用的这些退化性变化最好通过重组抑制区域选择效率的改变来解释。这些发现表明,粗糙脉孢菌为研究性调控染色体中重组抑制年轻区域的基因组退化性变化提供了一个有效的系统。