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转录因子 RBPJ 作为调节 Notch 反应的分子开关。

Transcription Factor RBPJ as a Molecular Switch in Regulating the Notch Response.

机构信息

Institute of Biochemistry, University of Giessen, Giessen, Germany.

Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

出版信息

Adv Exp Med Biol. 2021;1287:9-30. doi: 10.1007/978-3-030-55031-8_2.

Abstract

The Notch signal transduction cascade requires cell-to-cell contact and results in the proteolytic processing of the Notch receptor and subsequent assembly of a transcriptional coactivator complex containing the Notch intracellular domain (NICD) and transcription factor RBPJ. In the absence of a Notch signal, RBPJ remains at Notch target genes and dampens transcriptional output. Like in other signaling pathways, RBPJ is able to switch from activation to repression by associating with corepressor complexes containing several chromatin-modifying enzymes. Here, we focus on the recent advances concerning RBPJ-corepressor functions, especially in regard to chromatin regulation. We put this into the context of one of the best-studied model systems for Notch, blood cell development. Alterations in the RBPJ-corepressor functions can contribute to the development of leukemia, especially in the case of acute myeloid leukemia (AML). The versatile role of transcription factor RBPJ in regulating pivotal target genes like c-MYC and HES1 may contribute to the better understanding of the development of leukemia.

摘要

Notch 信号转导级联需要细胞间接触,导致 Notch 受体的蛋白水解加工,随后组装包含 Notch 细胞内结构域 (NICD) 和转录因子 RBPJ 的转录共激活复合物。在没有 Notch 信号的情况下,RBPJ 仍位于 Notch 靶基因上,并抑制转录输出。与其他信号通路一样,RBPJ 通过与包含几种染色质修饰酶的核心抑制复合物结合,能够从激活状态切换到抑制状态。在这里,我们重点介绍了关于 RBPJ-共抑制因子功能的最新进展,特别是在染色质调节方面。我们将其置于 Notch 研究最深入的模型系统之一——血细胞发育的背景下。RBPJ-共抑制因子功能的改变可能导致白血病的发生,尤其是急性髓系白血病 (AML)。转录因子 RBPJ 调节关键靶基因如 c-MYC 和 HES1 的多功能作用可能有助于更好地理解白血病的发生。

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