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Ancient origin of human complement factor H

机译:人类补体因子H的远古起源

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We studied the evolutionary history of two homologous proteins of the human complement system, factor H (FH) and the ct chain of the C4b binding protein (C4bp alpha), and included in this study the related proteins from the barred sand bass (P. nebulifer) and the nematode C. elegans, Phylogenetic trees inferred from individual short consensus repeats (SCRs) and divergence among repeats from different genes suggest that human FH has a much closer evolutionary relationship to putative complement components from P. nebulifer and C. elegans than does the C4bp alpha. This indicates that a member of the alternative pathway of the complement system (FH) has an ancient origin, while a homologous member of the classical pathway (C4bpa) appeared later in evolutionary history as a result of gene duplication. The ancient evolutionary position of FH is in agreement with the suggestion that the alternative pathway of the complement system is older than the classical pathway. Phylogenetic analysis also shows that the sand bass cofactor protein SBP1 and cofactor related protein SBCRP-1 have diverged very recently. [References: 32]
机译:我们研究了人类补体系统的两种同源蛋白H因子(FH)和C4b结合蛋白ct链(C4bp alpha)的进化史,并包括了禁止的鲈鱼(P.从单个短共有重复序列(SCR)推断出的系统发育树以及不同基因的重复序列之间的差异表明,与F. nebulifer和C. elegans的推定补体成分相比,人类FH与进化关系更紧密C4bp alpha。这表明补体系统(FH)的替代途径的成员起源很久,而经典途径(C4bpa)的同源成员由于基因复制而出现在进化史的后期。 FH在古代的进化地位与以下建议相符:补体系统的替代途径比经典途径古老。系统发育分析还显示,沙鲈辅因子蛋白SBP1和辅因子相关蛋白SBCRP-1最近已经分化。 [参考:32]

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