Complete sequence determination of the mouse and human CTLA4 gene loci: Cross-species DNA sequence similarity beyond exon borders

被引:62
作者
Ling, V
Wu, PW
Finnerty, HF
Sharpe, AH
Gray, GS
Collins, M
机构
[1] Genet Inst, Dept Immunol, Cambridge, MA 02140 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Div Immunol Res, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Boston, MA 02115 USA
关键词
D O I
10.1006/geno.1999.5930
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
CTLA4 (CD152), a receptor for the B7 costimulatory molecules (CD80 and CD86), is considered a fundamental regulator of T-cell activation. In this paper, we present the complete primary structure of the mouse and human CTLA4 gene loci. Sequence comparison between the mouse and the human CTLA4 gene loci revealed a high degree of sequence conservation both for homologous noncoding regions (65-78% identity) and for coding regions (72-98% identity), with an overall score of 71% over the entire length of the two genes. Of the CTLA4 genomic regions aligned, five simple repetitive elements were found in the mouse locus, whereas two simple repetitive sequences were localized on the human locus, RNA blot analysis of mouse and human primary tissues indicated that both CTLA4 and T-cell receptor transcripts were found in most organs with generally higher levels in lymphoid tissues. The conservation of CTLA4 gene patterning raises the possibility that constrained gene evolution of CTLA4 may be linked to conserved transcriptional control of this locus. (C) 1999 Academic Press.
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页码:341 / 355
页数:15
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