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T 细胞发育中的转录抑制因子、共抑制因子和染色质修饰酶。

Transcriptional repressors, corepressors and chromatin modifying enzymes in T cell development.

机构信息

Department of Immunology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Cytokine. 2011 Mar;53(3):271-81. doi: 10.1016/j.cyto.2010.11.013. Epub 2010 Dec 16.

DOI:10.1016/j.cyto.2010.11.013
PMID:21163671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3049313/
Abstract

Gene expression is regulated by the combined action of transcriptional activators and transcriptional repressors. Transcriptional repressors function by recruiting corepressor complexes containing histone-modifying enzymes to specific sites within DNA. Chromatin modifying complexes are subsequently recruited, either directly by transcriptional repressors, or indirectly via corepressor complexes and/or histone modifications, to remodel chromatin into either a transcription-friendly 'open' form or an inhibitory 'closed' form. Transcriptional repressors, corepressors and chromatin modifying complexes play critical roles throughout T cell development. Here, we highlight those genes that function to repress transcription and that have been shown to be required for T cell development.

摘要

基因表达受转录激活因子和转录阻遏因子的共同作用调控。转录阻遏因子通过募集包含组蛋白修饰酶的共抑制复合物到 DNA 中的特定位点起作用。随后,染色质修饰复合物被募集,或者直接由转录阻遏因子募集,或者间接通过共抑制复合物和/或组蛋白修饰募集,以将染色质重塑为转录友好的“开放”形式或抑制性的“关闭”形式。转录阻遏因子、共抑制因子和染色质修饰复合物在 T 细胞发育过程中发挥关键作用。在这里,我们重点介绍那些具有转录抑制功能并已被证明是 T 细胞发育所必需的基因。

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本文引用的文献

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Conditional deletion of histone deacetylase 1 in T cells leads to enhanced airway inflammation and increased Th2 cytokine production.条件性敲除 T 细胞中的组蛋白去乙酰化酶 1 导致气道炎症增强和 Th2 细胞因子产生增加。
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组蛋白去乙酰化酶抑制后全基因组 STAT3 结合分析揭示树突状细胞中的新靶基因。
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The zinc-finger protein MAZR is part of the transcription factor network that controls the CD4 versus CD8 lineage fate of double-positive thymocytes.锌指蛋白 MAZR 是转录因子网络的一部分,该网络控制双阳性胸腺细胞的 CD4 与 CD8 谱系命运。
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