FHR-4A:: a new factor H-related protein is encoded by the human FHR-4 gene

被引:41
作者
Józsi, M
Richter, H
Löschmann, I
Skerka, C
Buck, F
Beisiegel, U
Erdei, A
Zipfel, PF
机构
[1] Hans Knoll Inst Nat Prod Res, Dept Infect Biol, D-07745 Jena, Germany
[2] Univ Hamburg, Inst Cell Biol & Clin Neurobiol, Hamburg, Germany
[3] Univ Hamburg, Hosp Eppendorf, Med Clin, D-20246 Hamburg, Germany
[4] Eotvos Lorand Univ, Dept Immunol, Budapest, Hungary
关键词
factor H-related; FHR-4; complement; apoprotein; CCP domain;
D O I
10.1038/sj.ejhg.5201324
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 describe a new member of the human Factor H protein family, termed Factor H-related protein 4A (FHR-4A). The corresponding cDNA sequence was isolated and encodes a secreted protein of 559 amino acids, with a predicted molecular weight of 63.2 kDa. Apparently, this novel cDNA is derived from the human FHR-4 gene. Genetic analysis shows that the human FHR-4 gene is composed of 10 coding exons, and two distinct mRNA transcripts are derived from this gene by alternative splicing. The short FHR-4B form represents a truncated variant and encodes a secreted protein of five domains ( previously termed FHR-4). The long transcript encodes the novel FHR-4A protein that is composed of nine complement control protein (CCP) domains. A unique feature of FHR-4A is the tandem arrangement of four CCP domains forming a 'natural dimer' of the short isoform. The FHR-4A protein is identified in human plasma as a 86kDa protein. The difference between the predicted and observed molecular masses is explained by glycosylation. Comparison of the deduced protein sequence of FHR-4A with peptides from a 86kDa apolipoprotein described by us earlier suggests that the long form, FHR-4A, represents this apoprotein. In summary, FHR-4A is a new Factor H-related protein with a unique domain composition, that is, an internal duplication of four CCP domains. To our knowledge, FHR-4A provides the first evidence for alternative splicing among Factor H-related genes.
引用
收藏
页码:321 / 329
页数:9
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