Liu Hai-Jing, Tang Zhen-Xin, Han Xue-Min, Yang Zhi-Ling, Zhang Fu-Min, Yang Hai-Ling, Liu Yan-Jing, Zeng Qing-Yin
State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing, China University of Chinese Academy of Sciences, Beijing, China.
College of Biological Sciences and Biotechnology, Beijing Forestry University, Beijing, China.
Mol Biol Evol. 2015 Nov;32(11):2844-59. doi: 10.1093/molbev/msv156. Epub 2015 Jul 28.
Whole-genome duplication (WGD), or polyploidy, is a major force in plant genome evolution. A duplicate of all genes is present in the genome immediately following a WGD event. However, the evolutionary mechanisms responsible for the loss of, or retention and subsequent functional divergence of polyploidy-derived duplicates remain largely unknown. In this study we reconstructed the evolutionary history of the glutathione S-transferase (GST) gene family from the soybean genome, and identified 72 GST duplicated gene pairs formed by a recent Glycine-specific WGD event occurring approximately 13 Ma. We found that 72% of duplicated GST gene pairs experienced gene losses or pseudogenization, whereas 28% of GST gene pairs have been retained in the soybean genome. The GST pseudogenes were under relaxed selective constraints, whereas functional GSTs were subject to strong purifying selection. Plant GST genes play important roles in stress tolerance and detoxification metabolism. By examining the gene expression responses to abiotic stresses and enzymatic properties of the ancestral and current proteins, we found that polyploidy-derived GST duplicates show the divergence in enzymatic activities. Through site-directed mutagenesis of ancestral proteins, this study revealed that nonsynonymous substitutions of key amino acid sites play an important role in the divergence of enzymatic functions of polyploidy-derived GST duplicates. These findings provide new insights into the evolutionary and functional dynamics of polyploidy-derived duplicate genes.
全基因组复制(WGD),即多倍体现象,是植物基因组进化的主要驱动力。在WGD事件发生后,基因组中会立即出现所有基因的一个副本。然而,导致多倍体衍生副本丢失、保留以及随后功能分化的进化机制在很大程度上仍不为人知。在本研究中,我们重建了大豆基因组中谷胱甘肽S-转移酶(GST)基因家族的进化历史,并鉴定出72对由大约1300万年前发生的一次近期大豆属特异性WGD事件形成的GST重复基因对。我们发现,72%的重复GST基因对经历了基因丢失或假基因化,而28%的GST基因对保留在了大豆基因组中。GST假基因受到的选择限制较为宽松,而功能性GST则受到强烈的纯化选择。植物GST基因在胁迫耐受性和解毒代谢中发挥着重要作用。通过检测祖先蛋白和当前蛋白对非生物胁迫的基因表达响应及酶学特性,我们发现多倍体衍生的GST重复基因在酶活性上存在差异。通过对祖先蛋白进行定点诱变,本研究揭示关键氨基酸位点的非同义替换在多倍体衍生的GST重复基因的酶功能分化中起重要作用。这些发现为多倍体衍生重复基因的进化和功能动态提供了新的见解。