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Menin: a scaffold protein that controls gene expression and cell signaling

门1 支架蛋白 生物 转录因子 基因 细胞生物学 癌症研究 抑制器 信号转导 基因表达调控 遗传学 多发性内分泌肿瘤
作者
Smita Matkar,Austin Thiel,Xianxin Hua
出处
期刊:Trends in Biochemical Sciences [Elsevier BV]
卷期号:38 (8): 394-402 被引量:217
标识
DOI:10.1016/j.tibs.2013.05.005
摘要

•Molecular and structural basis for menin-mediated activation of gene transcription. •Multiple modes and molecular basis of menin-mediated suppression of gene transcription. •Menin regulates multiple cell signaling pathways. •Menin is regulated by multiple factors and signaling pathways. The protein menin is encoded by the MEN1 gene, which is mutated in patients with multiple endocrine neoplasia type 1 (MEN1) syndrome. Although menin acts as a tumor suppressor in endocrine organs, it is required for leukemic transformation in mouse models. Menin possesses these dichotomous functions probably because it can both positively and negatively regulate gene expression, as well as interact with a multitude of proteins with diverse functions. Here, we review the recent progress in understanding the molecular mechanisms by which menin functions. The crystal structures of menin with different binding partners reveal that menin is a key scaffold protein that functionally crosstalks with various partners to regulate gene transcription and interplay with multiple signaling pathways. The protein menin is encoded by the MEN1 gene, which is mutated in patients with multiple endocrine neoplasia type 1 (MEN1) syndrome. Although menin acts as a tumor suppressor in endocrine organs, it is required for leukemic transformation in mouse models. Menin possesses these dichotomous functions probably because it can both positively and negatively regulate gene expression, as well as interact with a multitude of proteins with diverse functions. Here, we review the recent progress in understanding the molecular mechanisms by which menin functions. The crystal structures of menin with different binding partners reveal that menin is a key scaffold protein that functionally crosstalks with various partners to regulate gene transcription and interplay with multiple signaling pathways.
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