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SUFU 的双重调控功能和 GLI2 的靶标组在 SHH 亚组髓母细胞瘤中的作用。

Dual Regulatory Functions of SUFU and Targetome of GLI2 in SHH Subgroup Medulloblastoma.

机构信息

Program in Developmental & Stem Cell Biology, The Hospital for Sick Children, Toronto, ON, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.

Program in Developmental & Stem Cell Biology, The Hospital for Sick Children, Toronto, ON, Canada.

出版信息

Dev Cell. 2019 Jan 28;48(2):167-183.e5. doi: 10.1016/j.devcel.2018.11.015. Epub 2018 Dec 13.

Abstract

SUFU alterations are common in human Sonic Hedgehog (SHH) subgroup medulloblastoma (MB). However, its tumorigenic mechanisms have remained elusive. Here, we report that loss of Sufu alone is unable to induce MB formation in mice, due to insufficient Gli2 activation. Simultaneous loss of Spop, an E3 ubiquitin ligase targeting Gli2, restores robust Gli2 activation and induces rapid MB formation in Sufu knockout background. We also demonstrated a tumor-promoting role of Sufu in Smo-activated MB (∼60% of human SHH MB) by maintaining robust Gli activity. Having established Gli2 activation as a key driver of SHH MB, we report a comprehensive analysis of its targetome. Furthermore, we identified Atoh1 as a target and molecular accomplice of Gli2 that activates core SHH MB signature genes in a synergistic manner. Overall, our work establishes the dual role of SUFU in SHH MB and provides mechanistic insights into transcriptional regulation underlying Gli2-mediated SHH MB tumorigenesis.

摘要

SUFU 改变在人类 Sonic Hedgehog (SHH) 亚组髓母细胞瘤 (MB) 中很常见。然而,其肿瘤发生机制仍然难以捉摸。在这里,我们报告说,由于Gli2 激活不足,单独缺失 Sufu 不足以在小鼠中诱导 MB 形成。同时缺失靶向 Gli2 的 E3 泛素连接酶 Spop,可恢复强烈的 Gli2 激活,并在 Sufu 敲除背景下迅速诱导 MB 形成。我们还通过维持强烈的 Gli 活性,证明了 Sufu 在 Smo 激活的 MB(约 60%的人类 SHH MB)中的促肿瘤作用。在确定 Gli2 激活作为 SHH MB 的关键驱动因素后,我们报告了对其靶蛋白组的全面分析。此外,我们鉴定出 Atoh1 是 Gli2 的靶标和分子同伙,以协同方式激活核心 SHH MB 特征基因。总的来说,我们的工作确立了 SUFU 在 SHH MB 中的双重作用,并为 Gli2 介导的 SHH MB 肿瘤发生的转录调控提供了机制见解。

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