GENOMIC ORGANIZATION OF HUMAN-COMPLEMENT COMPONENT-C3

被引:46
作者
FONG, KY
BOTTO, M
WALPORT, MJ
SO, AK
机构
[1] Rheumatology Unit, Department of Medicine, RPMS, London, W12 ONN, Du Cane Road
基金
英国惠康基金;
关键词
D O I
10.1016/0888-7543(90)90202-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Six overlapping clones, spanning the entire C3 gene and the 5′ flanking region, were isolated from two genomic λ libraries. Thirty exons, covering the complete β chain and part of the α chain as far as the C3d region, were analyzed. The full exon-intron organization of the gene was deduced by combining our data with the reported organization of the α′ chain (Barnum et al., 1989, J. Biol. Chem. 264: 8471-8474). The complete gene is 41 kb and consists of 41 exons. The C3 β chain spans 13 kb from exon 1 to exon 16. Exon 16 encodes both α and β chains. The α chain is 28 kb and contains 26 exons, including exon 16. The 5′ flanking region was sequenced up to 514 bases upstream from the ATG start site. The major transcription initiation site was mapped to an adenine residue 61 bases upstream from the signal peptide by primer extension analysis of poly(A)+ mRNA from hepatocytes and U937 cells. The TATA box motif was assigned at position-85. Several putative binding sites for transcription factors were found in the 5′ flanking region, suggesting possible pathways for the regulation of the C3 gene. © 1990.
引用
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页码:579 / 586
页数:8
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