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PML 通过稳定 MHC II 类转录激活子促进 MHC II 类基因的表达。

PML promotes MHC class II gene expression by stabilizing the class II transactivator.

机构信息

Leibniz Institute for Age Research, Fritz-Lipmann Institute, 07745 Jena, Germany.

出版信息

J Cell Biol. 2012 Oct 1;199(1):49-63. doi: 10.1083/jcb.201112015. Epub 2012 Sep 24.

Abstract

Promyelocytic leukemia (PML) nuclear bodies selectively associate with transcriptionally active genomic regions, including the gene-rich major histocompatibility (MHC) locus. In this paper, we have explored potential links between PML and interferon (IFN)-γ-induced MHC class II expression. IFN-γ induced a substantial increase in the spatial proximity between PML bodies and the MHC class II gene cluster in different human cell types. Knockdown experiments show that PML is required for efficient IFN-γ-induced MHC II gene transcription through regulation of the class II transactivator (CIITA). PML mediates this function through protection of CIITA from proteasomal degradation. We also show that PML isoform II specifically forms a stable complex with CIITA at PML bodies. These observations establish PML as a coregulator of IFN-γ-induced MHC class II expression.

摘要

早幼粒细胞白血病(PML)核体选择性地与转录活跃的基因组区域相关联,包括富含基因的主要组织相容性复合体(MHC)基因座。在本文中,我们探讨了 PML 与干扰素(IFN)-γ诱导的 MHC Ⅱ类表达之间的潜在联系。IFN-γ诱导 PML 体与不同人类细胞类型中的 MHC Ⅱ类基因簇之间的空间接近度显著增加。敲低实验表明,PML 通过调节 MHC II 类转录激活物(CIITA),是 IFN-γ诱导的 MHC II 类基因转录所必需的。PML 通过保护 CIITA 免受蛋白酶体降解来介导此功能。我们还表明,PML 同种型 II 特异性地在 PML 体上与 CIITA 形成稳定的复合物。这些观察结果确立了 PML 作为 IFN-γ诱导的 MHC Ⅱ类表达的核心调节因子。

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