Notch 二聚化的缺失会通过涉及 HDAC 活性的机制扰乱肠道稳态。

IF 4 2区 生物学 Q1 GENETICS & HEREDITY PLoS Genetics Pub Date : 2024-12-12 eCollection Date: 2024-12-01 DOI:10.1371/journal.pgen.1011486
Quanhui Dai, Kristina Preusse, Danni Yu, Rhett A Kovall, Konrad Thorner, Xinhua Lin, Raphael Kopan
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引用次数: 0

摘要

包含 NICD、RBPj 和 MAML1 的三蛋白复合物以单体或合作二聚体的形式与 DNA 结合,从而调节转录。表达Notch1和Notch2的Notch二聚化缺陷等位基因(NDD)的小鼠对环境损伤敏感,但在其他方面发育和衰老正常。结肠球体的转录组分析没有发现二聚体依赖性靶基因调控失误的证据,证实了体外干细胞维持能力受损,并发现了上皮先天性免疫对共生体的反应特征升高,这可能是 NDD 小鼠敏感性升高的根本原因。在表达 NOTCH2DD 或 NOTCH2 的人类结肠癌细胞系中进行 TurboID 之后的定量纳米喷雾 MS/MS 质谱分析,发现了一个不平衡的相互作用组,NOTCH2DD 与转录机制的相互作用减少,但与 HDAC2 相互作用组的相互作用相对保留,这表明通过合作性进行调节。为了弄清HDAC2的活性是否有助于Notch功能缺失表型的形成,我们使用了HDAC2抑制剂丙戊酸(VPA),发现它能防止NDD和γ分泌酶抑制剂(DBZ或DAPT)处理小鼠和球形细胞造成的肠道后果,这表明HDAC活性与肠道干细胞的促分化程序之间存在协同作用。
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Loss of Notch dimerization perturbs intestinal homeostasis by a mechanism involving HDAC activity.

A tri-protein complex containing NICD, RBPj and MAML1 binds DNA as monomer or as cooperative dimers to regulate transcription. Mice expressing Notch dimerization-deficient alleles (NDD) of Notch1 and Notch2 are sensitized to environmental insults but otherwise develop and age normally. Transcriptomic analysis of colonic spheroids uncovered no evidence of dimer-dependent target gene miss-regulation, confirmed impaired stem cell maintenance in-vitro, and discovered an elevated signature of epithelial innate immune response to symbionts, a likely underlying cause for heightened sensitivity in NDD mice. TurboID followed by quantitative nano-spray MS/MS mass-spectrometry analyses in a human colon carcinoma cell line expressing either NOTCH2DD or NOTCH2 revealed an unbalanced interactome, with reduced interaction of NOTCH2DD with the transcription machinery but relatively preserved interaction with the HDAC2 interactome suggesting modulation via cooperativity. To ask if HDAC2 activity contributes to Notch loss-of-function phenotypes, we used the HDAC2 inhibitor Valproic acid (VPA) and discovered it could prevent the intestinal consequences of NDD and gamma secretase inhibitors (DBZ or DAPT) treatment in mice and spheroids, suggesting synergy between HDAC activity and pro-differentiation program in intestinal stem cells.

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PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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