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CD4-CD8-至CD4+CD8+胸腺细胞分化过程中TCR-β基因座染色质变化的生化与功能分析。

Biochemical and functional analyses of chromatin changes at the TCR-beta gene locus during CD4-CD8- to CD4+CD8+ thymocyte differentiation.

作者信息

Chattopadhyay S, Whitehurst C E, Schwenk F, Chen J

机构信息

Center for Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

J Immunol. 1998 Feb 1;160(3):1256-67.

PMID:9570542
Abstract

Allelic exclusion is the process wherein lymphocytes express Ag receptors from only one of two possible alleles, and is effected through a feedback inhibition of further rearrangement of the second allele. The feedback signal is thought to cause chromatin changes that block accessibility of the second allele to the recombinase. To identify the putative chromatin changes associated with allelic exclusion, we assayed for DNase I hypersensitivity, DNA methylation, and transcription in 100 kb of the TCR-beta locus. Contrary to current models, we identified chromatin changes indicative of an active and accessible locus associated with the occurrence of allelic exclusion. Of 11 DNase I hypersensitive sites identified, 3 were induced during CD4-CD8- to CD4+CD8+ thymocyte differentiation, and demethylation and increased germline transcription of the locus were evident. We further examined the role of the most prominently induced site near the TCR-beta enhancer (E beta) in allelic exclusion by targeted mutagenesis. Two other sites were also examined in New Zealand White (NZW) mice that have a natural deletion in the TCR-beta locus. TCR-beta gene recombination and allelic exclusion were normal in both mutant mice, negating dominant roles for the three hypersensitive sites in the control of allelic exclusion. The data suggest that alternative cis-regulatory elements, perhaps contained in the E beta enhancer and/or in the upstream V beta region, are involved in the control of TCR-beta allelic exclusion.

摘要

等位基因排斥是淋巴细胞仅从两个可能的等位基因中的一个表达抗原受体的过程,并且通过对第二个等位基因进一步重排的反馈抑制来实现。反馈信号被认为会引起染色质变化,从而阻止第二个等位基因与重组酶的接触。为了确定与等位基因排斥相关的假定染色质变化,我们检测了TCR-β基因座100 kb区域内的DNA酶I超敏性、DNA甲基化和转录情况。与当前模型相反,我们发现了与等位基因排斥发生相关的、指示活跃且可及基因座的染色质变化。在鉴定出的11个DNA酶I超敏位点中,有3个是在CD4-CD8-到CD4+CD8+胸腺细胞分化过程中诱导产生的,并且该基因座的去甲基化和种系转录增加是明显的。我们通过靶向诱变进一步研究了TCR-β增强子(Eβ)附近最显著诱导位点在等位基因排斥中的作用。还在TCR-β基因座存在天然缺失的新西兰白兔(NZW)小鼠中检测了另外两个位点。两种突变小鼠中的TCR-β基因重组和等位基因排斥均正常,否定了这三个超敏位点在等位基因排斥控制中的主导作用。数据表明,可能包含在Eβ增强子和/或上游Vβ区域中的替代顺式调控元件参与了TCR-β等位基因排斥的控制。

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