Ancient origin of human complement factor H

被引:23
作者
Krushkal, J
Kemper, C
Gigli, I
机构
[1] Univ Texas, Hlth Sci Ctr, Res Ctr Human Genet, Inst Mol Med Prevent Human Dis, Houston, TX 77030 USA
[2] Univ Texas, Hlth Sci Ctr, Res Ctr Immunol & Autoimmune Dis, Inst Mol Med Prevent Human Dis, Houston, TX 77030 USA
关键词
complement system; C4b binding protein; factor H; sand bass cofactor protein; sand bass cofactor-related protein 1; short consensus repeats;
D O I
10.1007/PL00013152
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:625 / 630
页数:6
相关论文
共 32 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   GENES FOR C4B-BINDING PROTEIN A-CHAINS AND BETA-CHAINS (C4BPA AND C4BPB) ARE LOCATED ON CHROMOSOME-1, BAND-1Q32, IN HUMANS AND ON CHROMOSOME-13 IN RATS [J].
ANDERSSON, A ;
DAHLBACK, B ;
HANSON, C ;
HILLARP, A ;
LEVAN, G ;
SZPIRER, J ;
SZPIRER, C .
SOMATIC CELL AND MOLECULAR GENETICS, 1990, 16 (05) :493-500
[3]  
DAHA MR, 1982, J IMMUNOL, V128, P1839
[4]   CLONING AND CHARACTERIZATION OF A CDNA REPRESENTING A PUTATIVE COMPLEMENT-REGULATORY PLASMA-PROTEIN FROM BARRED SAND BASS (PARABLAX NEBLIFER) [J].
DAHMEN, A ;
KAIDOH, T ;
ZIPFEL, PF ;
GIGLI, I .
BIOCHEMICAL JOURNAL, 1994, 301 :391-397
[5]   THE GENE CODING FOR THE BETA-CHAIN OF C4B-BINDING PROTEIN (C4BPB) HAS BECOME A PSEUDOGENE IN THE MOUSE [J].
DECORDOBA, SR ;
PEREZBLAS, M ;
RAMOSRUIZ, R ;
SANCHEZCORRAL, P ;
DEVILLENA, FPM ;
REYCAMPOS, J .
GENOMICS, 1994, 21 (03) :501-509
[6]  
Felsenstein J, 1993, PHYLIP (Phylogeny Inference Package) version 3.5c
[7]   MODULATION OF THE CLASSICAL PATHWAY C-3 CONVERTASE BY PLASMA-PROTEINS C-4 BINDING-PROTEIN AND C3B INACTIVATOR [J].
GIGLI, I ;
FUJITA, T ;
NUSSENZWEIG, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (12) :6596-6600
[8]  
Hillarp A, 1997, J IMMUNOL, V158, P1315
[9]  
HILLARP A, 1988, J BIOL CHEM, V263, P12759
[10]  
HORSTMANN RD, 1985, J IMMUNOL, V134, P1094