European Molecular Biology Laboratory-Centre for Genomic Regulation Systems Biology Unit, Centre for Genomic Regulation, Barcelona, Spain.
PLoS One. 2010 Mar 10;5(3):e9474. doi: 10.1371/journal.pone.0009474.
Dosage sensitivity is an important evolutionary force which impacts on gene dispensability and duplicability. The newly available data on human copy-number variation (CNV) allow an analysis of the most recent and ongoing evolution. Provided that heterozygous gene deletions and duplications actually change gene dosage, we expect to observe negative selection against CNVs encompassing dosage sensitive genes. In this study, we make use of several sources of population genetic data to identify selection on structural variations of dosage sensitive genes. We show that CNVs can directly affect expression levels of contained genes. We find that genes encoding members of protein complexes exhibit limited expression variation and overlap significantly with a manually derived set of dosage sensitive genes. We show that complexes and other dosage sensitive genes are underrepresented in CNV regions, with a particular bias against frequent variations and duplications. These results suggest that dosage sensitivity is a significant force of negative selection on regions of copy-number variation.
剂量敏感性是一种重要的进化力量,它影响基因的非必需性和可复制性。新获得的人类拷贝数变异(CNV)数据允许对最近和正在进行的进化进行分析。如果杂合子基因缺失和重复实际上改变了基因剂量,我们预计会观察到对包含剂量敏感基因的 CNV 的负选择。在这项研究中,我们利用多种群体遗传数据来源来识别对剂量敏感基因结构变异的选择。我们表明,CNV 可以直接影响包含基因的表达水平。我们发现,编码蛋白复合物成员的基因表现出有限的表达变化,并且与人工衍生的一组剂量敏感基因显著重叠。我们表明,复合物和其他剂量敏感基因在 CNV 区域中代表性不足,特别是对频繁的变异和重复存在偏见。这些结果表明,剂量敏感性是对拷贝数变异区域的负选择的一个重要力量。