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MYCN 癌基因蛋白是核外切体靶向复合物的 RNA 结合辅助因子。

The MYCN oncoprotein is an RNA-binding accessory factor of the nuclear exosome targeting complex.

机构信息

Theodor Boveri Institute, Department of Biochemistry and Molecular Biology, Biocenter, University of Würzburg, Am Hubland, 97074 Würzburg, Germany; Mildred Scheel Early Career Center, University Hospital Würzburg, Josef-Schneider-Str. 6, 97080 Würzburg, Germany.

Theodor Boveri Institute, Department of Biochemistry and Molecular Biology, Biocenter, University of Würzburg, Am Hubland, 97074 Würzburg, Germany.

出版信息

Mol Cell. 2024 Jun 6;84(11):2070-2086.e20. doi: 10.1016/j.molcel.2024.04.007. Epub 2024 May 3.

Abstract

The MYCN oncoprotein binds active promoters in a heterodimer with its partner protein MAX. MYCN also interacts with the nuclear exosome, a 3'-5' exoribonuclease complex, suggesting a function in RNA metabolism. Here, we show that MYCN forms stable high-molecular-weight complexes with the exosome and multiple RNA-binding proteins. MYCN binds RNA in vitro and in cells via a conserved sequence termed MYCBoxI. In cells, MYCN associates with thousands of intronic transcripts together with the ZCCHC8 subunit of the nuclear exosome targeting complex and enhances their processing. Perturbing exosome function results in global re-localization of MYCN from promoters to intronic RNAs. On chromatin, MYCN is then replaced by the MNT(MXD6) repressor protein, inhibiting MYCN-dependent transcription. RNA-binding-deficient alleles show that RNA-binding limits MYCN's ability to activate cell growth-related genes but is required for MYCN's ability to promote progression through S phase and enhance the stress resilience of neuroblastoma cells.

摘要

MYCN 癌基因蛋白与其伴侣蛋白 MAX 形成异二聚体结合活性启动子。MYCN 还与核 exosome(一种 3'-5' 外切核酸酶复合物)相互作用,表明其在 RNA 代谢中具有功能。在这里,我们表明 MYCN 与 exosome 和多个 RNA 结合蛋白形成稳定的高分子量复合物。MYCN 通过一个称为 MYCBoxI 的保守序列在体外和细胞内结合 RNA。在细胞中,MYCN 与数千个内含子转录本一起与核 exosome 靶向复合物的 ZCCHC8 亚基结合,并增强其加工。干扰 exosome 的功能会导致 MYCN 从启动子全局重新定位到内含子 RNA。在染色质上,MYCN 随后被 MNT(MXD6)抑制蛋白取代,抑制 MYCN 依赖性转录。RNA 结合缺陷等位基因表明,RNA 结合限制了 MYCN 激活与细胞生长相关基因的能力,但对于 MYCN 促进 S 期进展和增强神经母细胞瘤细胞应激弹性的能力是必需的。

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