Evolutionary analysis of two complement C4 genes: Ancient duplication and conservation during jawed vertebrate evolution

被引:9
|
作者
Nonaka, Mayumi I. [1 ]
Terado, Tokio [2 ,3 ]
Kimura, Hiroshi [2 ]
Nonaka, Masaru [1 ]
机构
[1] Univ Tokyo, Biol Sci, Grad Sch Sci, Tokyo, Japan
[2] Shiga Univ Med Sci, Dept Mol Genet Med, Otsu, Shiga, Japan
[3] Shiga Univ Med Sci, Dept Biochem & Mol Biol, Otsu, Shiga, Japan
关键词
Complement C4; Classical pathway; Shark; Isotype; Gene duplication; Evolution; NURSE SHARK; COMPARATIVE GENOMICS; INTERNAL THIOESTER; MOLECULAR-CLONING; 4TH COMPONENT; FACTOR-B; SYSTEM; MHC; REGION; ORGANIZATION;
D O I
10.1016/j.dci.2016.11.009
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
The complement C4 is a thioester-containing protein, and a histidine (H) residue catalyzes the cleavage of the thioester to allow covalent binding to carbohydrates on target cells. Some mammalian and teleost species possess an additional isotype where the catalytic H is replaced by an aspartic acid (D), which binds preferentially to proteins. We found the two C4 isotypes in many other jawed vertebrates, including sharks and birds/reptiles. Phylogenetic analysis suggested that C4 gene duplication occurred in the early days of the jawed vertebrate evolution. The D-type C4 of bony fish except for mammals formed a cluster, termed D-lineage. The D-lineage genes were located in a syhtenic region outside MHC, and evolved conservatively. Mammals lost the D-lineage before speciation, but D-type C4 was regenerated by recent gene duplication in some mammalian species or groups. Dual C4 molecules with different substrate specificities would have contributed to development of the antibody-dependent classical pathway. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 11
页数:11
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