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SET8 通过非甲基化依赖的方式成为 TGF-β 信号的新型负调控因子。

SET8 is a novel negative regulator of TGF-β signaling in a methylation-independent manner.

机构信息

Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.

Department of Pathobiology, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, 467-8603, Japan.

出版信息

Sci Rep. 2023 Dec 18;13(1):22877. doi: 10.1038/s41598-023-49961-x.

Abstract

Transforming growth factor β (TGF-β) is a multifunctional cytokine that induces a diverse set of cellular processes principally through Smad-dependent transcription. Transcriptional responses induced by Smads are tightly regulated by Smad cofactors and histone modifications; however, the underlying mechanisms have not yet been elucidated in detail. We herein report lysine methyltransferase SET8 as a negative regulator of TGF-β signaling. SET8 physically associates with Smad2/3 and negatively affects transcriptional activation by TGF-β in a catalytic activity-independent manner. The depletion of SET8 results in an increase in TGF-β-induced plasminogen activator inhibitor-1 (PAI-1) and p21 expression and enhances the antiproliferative effects of TGF-β. Mechanistically, SET8 occupies the PAI-1 and p21 promoters, and a treatment with TGF-β triggers the replacement of the suppressive binding of SET8 with p300 on these promoters, possibly to promote gene transcription. Collectively, the present results reveal a novel role for SET8 in the negative regulation of TGF-β signaling.

摘要

转化生长因子 β(TGF-β)是一种多功能细胞因子,主要通过 Smad 依赖性转录诱导多种细胞过程。Smads 诱导的转录反应受 Smad 共因子和组蛋白修饰的严格调控;然而,其潜在的机制尚未详细阐明。我们在此报告赖氨酸甲基转移酶 SET8 是 TGF-β 信号的负调节剂。SET8 与 Smad2/3 物理结合,并以非催化活性依赖性方式负调控 TGF-β 的转录激活。SET8 的耗竭导致 TGF-β 诱导的纤溶酶原激活物抑制剂-1(PAI-1)和 p21 表达增加,并增强 TGF-β 的抗增殖作用。在机制上,SET8 占据 PAI-1 和 p21 启动子,TGF-β 处理触发抑制性 SET8 与这些启动子上的 p300 的结合被取代,可能促进基因转录。总之,本研究结果揭示了 SET8 在 TGF-β 信号负调控中的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c186/10739863/fee5e6b6e07c/41598_2023_49961_Fig1_HTML.jpg

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