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Bayesian phylogeny analysis of vertebrate serpins illustrates evolutionary conservation of the intron and indels based six groups classification system from lampreys for ∼500 MY

机译:脊椎动物丝氨酸蛋白酶抑制剂的贝叶斯系统发育分析说明了从七and鳗中以内含子和插入缺失为基础的六类分类系统的进化保守性约为500 MY

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摘要

The serpin superfamily is characterized by proteins that fold into a conserved tertiary structure and exploits a sophisticated and irreversible suicide-mechanism of inhibition. Vertebrate serpins are classified into six groups (V1–V6), based on three independent biological features—genomic organization, diagnostic amino acid sites and rare indels. However, this classification system was based on the limited number of mammalian genomes available. In this study, several non-mammalian genomes are used to validate this classification system using the powerful Bayesian phylogenetic method. This method supports the intron and indel based vertebrate classification and proves that serpins have been maintained from lampreys to humans for about 500 MY. Lampreys have fewer than 10 serpins, which expand into 36 serpins in humans. The two expanding groups V1 and V2 have SERPINB1/SERPINB6 and SERPINA8/SERPIND1 as the ancestral serpins, respectively. Large clusters of serpins are formed by local duplications of these serpins in tetrapod genomes. Interestingly, the ancestral HCII/SERPIND1 locus (nested within PIK4CA) possesses group V4 serpin (A2APL1, homolog of α2-AP/SERPINF2) of lampreys; hence, pointing to the fact that group V4 might have originated from group V2. Additionally in this study, details of the phylogenetic history and genomic characteristics of vertebrate serpins are revisited.
机译:丝氨酸蛋白酶抑制剂超家族的特征在于蛋白质,其折叠成保守的三级结构,并利用复杂而不可逆的自杀机制进行抑制。基于三个独立的生物学特征-基因组组织,诊断性氨基酸位点和稀有插入缺失,脊椎动物丝氨酸蛋白酶抑制剂被分为六类(V1-V6)。但是,该分类系统基于有限数量的可用哺乳动物基因组。在这项研究中,使用强大的贝叶斯系统发育方法,使用了几个非哺乳动物基因组来验证该分类系统。该方法支持基于内含子和插入缺失的脊椎动物分类,并证明丝氨酸蛋白酶抑制蛋白从七rey鳗到人类维持了大约500 MY的时间。 rey鳗的少于10个丝氨酸蛋白酶抑制剂,在人类中扩展为36个丝氨酸蛋白酶抑制剂。两个扩展组V1和V2分别具有SERPINB1 / SERPINB6和SERPINA8 / SERPIND1作为祖先serpin。丝氨酸蛋白酶抑制剂的大簇是由这些丝氨酸蛋白酶抑制剂在四足动物基因组中的局部复制形成的。有趣的是,祖先的HCII / SERPIND1基因座(嵌套在PIK4CA中)拥有七lamp鳗的V4丝氨酸蛋白酶抑制剂组(A2APL1,α2-AP/ SERPINF2的同源物)。因此,指出了第V4组可能源自第V2组这一事实。此外,在这项研究中,重新审视了脊椎动物丝氨酸蛋白酶抑制剂的系统发生历史和基因组特征。

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