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Menin 通路的表观遗传调控。

Epigenetic regulation by the menin pathway.

机构信息

Department of Cancer BiologyAbramson Family Cancer Research Institute, Abramson Cancer Center, Institute of Diabetes, Obesity, and Metabolism (IDOM), University of Pennsylvania, Philadelphia, Pennsylvania, USA.

State Key Laboratory of Veterinary BiotechnologyHarbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, Heilongjiang, China.

出版信息

Endocr Relat Cancer. 2017 Oct;24(10):T147-T159. doi: 10.1530/ERC-17-0298. Epub 2017 Aug 15.

Abstract

There is a trend of increasing prevalence of neuroendocrine tumors (NETs), and the inherited multiple endocrine neoplasia type 1 (MEN1) syndrome serves as a genetic model to investigate how NETs develop and the underlying mechanisms. Menin, encoded by the gene, at least partly acts as a scaffold protein by interacting with multiple partners to regulate cellular homeostasis of various endocrine organs. Menin has multiple functions including regulation of several important signaling pathways by controlling gene transcription. Here, we focus on reviewing the recent progress in elucidating the key biochemical role of menin in epigenetic regulation of gene transcription and cell signaling, as well as posttranslational regulation of menin itself. In particular, we will review the progress in studying structural and functional interactions of menin with various histone modifiers and transcription factors such as MLL, PRMT5, SUV39H1 and other transcription factors including c-Myb and JunD. Moreover, the role of menin in regulating cell signaling pathways such as TGF-beta, Wnt and Hedgehog, as well as miRNA biogenesis and processing will be described. Further, the regulation of the gene transcription, posttranslational modifications and stability of menin protein will be reviewed. These various modes of regulation by menin as well as regulation of menin by various biological factors broaden the view regarding how menin controls various biological processes in neuroendocrine organ homeostasis.

摘要

神经内分泌肿瘤 (NETs) 的发病率呈上升趋势,遗传性多发性内分泌腺瘤病 1 型 (MEN1) 综合征是研究 NETs 发生发展及其潜在机制的遗传模型。MEN1 基因编码的 menin 至少部分作为支架蛋白通过与多个伴侣相互作用来调节各种内分泌器官的细胞内稳态。menin 具有多种功能,包括通过控制基因转录来调节几个重要的信号通路。在这里,我们重点回顾阐明 menin 在基因转录的表观遗传调控和细胞信号转导以及自身翻译后调控中的关键生化作用的最新进展。特别是,我们将回顾研究 menin 与各种组蛋白修饰酶和转录因子(如 MLL、PRMT5、SUV39H1 和其他转录因子,包括 c-Myb 和 JunD)之间结构和功能相互作用的进展。此外,还将描述 menin 在调节 TGF-β、Wnt 和 Hedgehog 等细胞信号通路以及 miRNA 生物发生和加工中的作用。此外,还将回顾 menin 基因转录、menin 蛋白翻译后修饰和稳定性的调节。menin 的这些各种调节方式以及各种生物因素对 menin 的调节拓宽了人们对 menin 如何控制神经内分泌器官稳态中各种生物学过程的认识。

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