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免疫球蛋白μ重链增强子处ETS蛋白依赖性的可及性变化

ETS protein-dependent accessibility changes at the immunoglobulin mu heavy chain enhancer.

作者信息

Nikolajczyk B S, Sanchez J A, Sen R

机构信息

Rosenstiel Research Center and Department of Biology, Brandeis University, Waltham, Massachusetts 02454, USA.

出版信息

Immunity. 1999 Jul;11(1):11-20. doi: 10.1016/s1074-7613(00)80077-1.

Abstract

Directed accessibility mediated by antigen-receptor gene enhancers ensures developmental stage-specific activation of V(D)J recombination. Here, we used a combination of in vitro and in vivo assays to explore the mechanisms that regulate immunoglobulin mu heavy chain gene enhancer-dependent chromatin accessibility. Ets-1 or PU.1 bound to mu enhancer-containing plasmids assembled into chromatin in vitro and increased restriction enzyme access to a proximal site. In complementary analyses, expression of PU.1 in Ets-1-containing 2017 pro-T cells or NIH 3T3 cells induced sterile I mu transcripts at the IgH locus and increased accessibility of the endogenous mu enhancer to restriction endonucleases. These observations suggest that one role of PU.1 is to increase accessibility of the mu locus to initiate heavy chain gene expression.

摘要

由抗原受体基因增强子介导的定向可及性确保了V(D)J重组的发育阶段特异性激活。在这里,我们使用体外和体内试验相结合的方法来探索调节免疫球蛋白μ重链基因增强子依赖性染色质可及性的机制。Ets-1或PU.1与含有μ增强子的质粒结合,在体外组装成染色质,并增加了限制酶对近端位点的可及性。在互补分析中,在含有Ets-1的2017原T细胞或NIH 3T3细胞中表达PU.1会在IgH位点诱导无菌Iμ转录本,并增加内源性μ增强子对限制性内切酶的可及性。这些观察结果表明,PU.1的一个作用是增加μ基因座的可及性,以启动重链基因表达。

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