Evidence for distinct CD4 silencer functions at different stages of thymocyte differentiation

被引:104
作者
Taniuchi, I
Sunshine, MJ
Festenstein, R
Littman, DR
机构
[1] NYU, Sch Med, Skirball Inst Biomol Med, Howard Hughes Med Inst,Mol Pathogenesis Program, New York, NY 10016 USA
[2] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp,Sch Med, MRC,Clin Sci Ctr, Dept Med Gene Control Mech & Dis, London, England
关键词
D O I
10.1016/S1097-2765(02)00735-9
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
An intronic silencer within the CD4 gene is the critical cis regulatory element for T cell subset-specific expression of CD4. We have combined transfection studies with gene targeting in mice to identify several key sequences within the silencer core that are required for gene silencing during thymocyte development. In mice, mutations in individual sites resulted in variegated, but heritable, derepression of CD4 in mature CD8(+) T lymphocytes, whereas compound mutations resulted in full derepression. These results indicate that there is partial redundancy in recruiting a chromatin remodeling machinery that results in epigenetic silencing. Mutations in single sites also resulted in partial derepression of CD4 in immature double-negative thymocytes, but there was no apparent variegation. These findings suggest two distinct modes of CD4 silencer function at different developmental stages: active repression in CD4(-)CD8(-) thymocytes, in which silencing must be reversible, and epigenetic gene silencing upon differentiation to the CD8(+) cytotoxic T cell lineage.
引用
收藏
页码:1083 / 1096
页数:14
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