GENOMIC ORGANIZATION OF THE ALPHA-CHAIN OF THE HUMAN C4B-BINDING PROTEIN GENE

被引:13
作者
ASO, T
OKAMURA, S
MATSUGUCHI, T
SAKAMOTO, N
SATA, T
NIHO, Y
机构
[1] KYUSHU UNIV,FAC MED,DEPT INTERNAL MED 1,FUKUOKA 812,JAPAN
[2] KYUSHU UNIV,FAC MED,CTR CANC,FUKUOKA 812,JAPAN
[3] KYUSHU UNIV,FAC MED,GENET INFORMAT RES LAB,FUKUOKA 812,JAPAN
[4] SATA CLIN,FUKUOKA,JAPAN
关键词
D O I
10.1016/0006-291X(91)90509-6
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
C4b-binding protein (C4bp) is a serum glycoprotein that is one of the regulators of the complement activation (RCA) family. This protein is composed of structurally related 70-kDa (α chain) and 45-kDa (β chain) polypeptides. The α chain of C4bp (C4bpα) consists of eight short consensus repeats (SCR), which constitute the amino-terminal 491 residues. Human C4bp is also one of the acute-phase reactants. In order to clarify the genetic basis of the SCR and to understand the regulatory mechanisms of C4bp synthesis, we isolated 6 genomic DNA clones covering all of the human C4bpα gene. This gene consists of 12 exons and spans about 40 kb. Each of the SCRs is encoded by a single exon, except for the second SCR (SCR II), which is encoded by two separate exons, demonstrating that human C4bpα has a split SCR at the genomic level. The 5′ flanking region was sequenced up to 380 bases upstream from the putative transcription initiation site. Several possible binding sites for transcription factors were identified. © 1991.
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页码:222 / 227
页数:6
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