Weis J J, Toothaker L E, Smith J A, Weis J H, Fearon D T
Department of Rheumatology and Immunology, Brigham and Women's Hospital, Boston, Massachusetts.
J Exp Med. 1988 Mar 1;167(3):1047-66. doi: 10.1084/jem.167.3.1047.
Human complement receptor type 2 (CR2) is the B lymphocyte receptor for C3d and the Epstein-Barr virus. This protein is also a member of a family of C3b/C4b binding proteins that regulate complement activation, comprise tandemly repeated 60-75 amino acid sequences, and whose genes map to band q32 on chromosome 1. Overlapping cDNA clones encoding the entire human CR2 protein have been isolated from a human tonsillar cDNA library. The derived amino acid sequence of 1,032 residues encodes a peptide of 112,716 mol wt. A signal peptide was identified, followed by 15 copies of the short consensus repeat (SCR) structure common to the C3/C4 binding protein family. The entire extracellular portion of the protein comprised SCRs, thus, the ligand binding sites both for C3d and the EBV protein gp350/220 are positioned within this structure. Immediately following the final SCR was a transmembrane sequence of 24 amino acids and a cytoplasmic region of 34 amino acids. One of five cDNA clones isolated contained an additional SCR, providing evidence for alternative mRNA splicing or gene products of different human alleles. The CR2 cDNAs were used to isolate CR2-specific genomic phage. The entire CR2 coding sequences were found within 20 kb of human DNA. Analysis of the CR2 cDNA sequence indicated that CR2 contained internally homologous regions and suggested that CR2 arose by duplication of a primordial gene sequence encoding four SCRs. Comparison of the CR2 peptide sequence with those of other members of the gene family has identified many regions highly homologous with human CR1, fewer with C4bp and decay accelerating factor, and very few with factor H, and suggested that CR2 and CR1 arose by duplication of the same ancestral gene sequence. The homology between CR2 and CR1 extended to the transmembrane and cytoplasmic regions, suggesting that these sequences were derived from a common membrane-bound precursor.
人类2型补体受体(CR2)是C3d和爱泼斯坦-巴尔病毒的B淋巴细胞受体。该蛋白也是C3b/C4b结合蛋白家族的成员之一,这些蛋白调节补体激活,包含串联重复的60-75个氨基酸序列,其基因定位于1号染色体的q32带。从人扁桃体cDNA文库中分离出了编码整个人类CR2蛋白的重叠cDNA克隆。推导的1032个残基的氨基酸序列编码一个分子量为112,716的肽。鉴定出一个信号肽,其后是C3/C4结合蛋白家族共有的15个短共有重复序列(SCR)结构拷贝。该蛋白的整个细胞外部分都由SCR组成,因此,C3d和EBV蛋白gp350/220的配体结合位点都位于该结构内。在最后一个SCR之后紧接着是一个24个氨基酸的跨膜序列和一个34个氨基酸的细胞质区域。分离出的五个cDNA克隆之一包含一个额外的SCR,这为不同人类等位基因的可变mRNA剪接或基因产物提供了证据。CR2 cDNA被用于分离CR2特异性基因组噬菌体。发现整个人类CR2编码序列位于20 kb的人类DNA内。对CR2 cDNA序列的分析表明,CR2包含内部同源区域,并提示CR2是由编码四个SCR的原始基因序列重复产生的。将CR2肽序列与该基因家族其他成员的序列进行比较,发现与人类CR1有许多高度同源的区域,与C4bp和衰变加速因子的同源区域较少,与因子H的同源区域极少,并提示CR2和CR1是由相同的祖先基因序列重复产生的。CR2和CR1之间的同源性延伸到跨膜和细胞质区域,表明这些序列来自共同的膜结合前体。