Liu Qingpo, Xue Qingzhong
Department of Agronomy, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310029, P. R. China.
J Mol Evol. 2007 Mar;64(3):354-63. doi: 10.1007/s00239-006-0131-x. Epub 2007 Jan 16.
The identification of LSD1-like genes in parasite, green algae, moss, pine, and monocot and dicot species allowed us to trace the phylogenetic history of this gene family. Computational analysis showed that the diversification of members of this family could be dated back to the early stage of plant evolution. The evolution of plant LSD1-like genes was possibly shaped by two duplication events. These proteins, which contain three copies of the LSD1 zinc finger (zf-LSD1) domain within their entire polypeptides and play crucial roles in modulating disease defense and cell death, resulted from the second duplication. A gain of zf-LSD1 domain model was reasonable for explaining the origination of three-zf-LSD1 domain-containing proteins. The zf-LSD1 domain phylogeny showed that the middle (M) and C-terminal (C) domains originated from a common ancestor; the N-terminal (N) domain might be more ancient than the former two. The divergence of the N, M, and C domains was well before the monocot-dicot split. Coevolution analysis revealed that four intramolecular domain pairs, including the N domain and the interregion between the M and the C domains (INTER2), the M and C domain, the N- and C-terminus, and the M domain and C-terminus, possibly coevolved during the evolution of three-zf-LSD1 domain-containing proteins. The three zf-LSD1 domains are evolutionary conserved. Thus, the differences at the N- and C-terminus would be crucial for functional specificity of LSD1 genes. Strong functional constraints should work on the zf-LSD1 domains, whereas reduced functional constraint was found in the INTER2 region. Functional divergence analysis showed that three-zf-LSD1 domain-containing proteins were significantly functionally divergent from those proteins containing only one zf-LSD1 domain, a result demonstrating that shifted evolutionary rates between the two clusters were significantly different from each other.
在寄生虫、绿藻、苔藓、松树以及单子叶和双子叶植物物种中鉴定出类LSD1基因,这使我们能够追溯该基因家族的系统发育历史。计算分析表明,该家族成员的多样化可追溯到植物进化的早期阶段。植物类LSD1基因的进化可能受到两次复制事件的影响。这些蛋白质在其整个多肽中包含三个LSD1锌指(zf-LSD1)结构域拷贝,在调节疾病防御和细胞死亡中起关键作用,是第二次复制的结果。zf-LSD1结构域获得模型合理地解释了含三个zf-LSD1结构域的蛋白质的起源。zf-LSD1结构域系统发育表明,中间(M)和C末端(C)结构域起源于一个共同祖先;N末端(N)结构域可能比前两者更古老。N、M和C结构域的分化早于单子叶植物和双子叶植物的分化。共进化分析表明,四个分子内结构域对,包括N结构域与M和C结构域之间的区域(INTER2)、M和C结构域、N和C末端以及M结构域和C末端,可能在含三个zf-LSD1结构域的蛋白质进化过程中共进化。三个zf-LSD1结构域在进化上是保守的。因此,N和C末端的差异对于LSD1基因的功能特异性至关重要。强大的功能限制应该作用于zf-LSD1结构域,而在INTER2区域发现功能限制有所降低。功能分化分析表明,含三个zf-LSD1结构域的蛋白质与仅含一个zf-LSD1结构域的蛋白质在功能上有显著差异,这一结果表明两个簇之间的进化速率变化彼此显著不同。