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揭示含SET结构域的哺乳动物蛋白4

Unmasking the mammalian SET domain-containing protein 4.

作者信息

Wang Yuan, Shen Zhiyuan

机构信息

Rutgers Cancer Institute of New Jersey, Department of Radiation Oncology, Rutgers Robert Wood Johnson Medical School, 195 Little Albany Street, New Brunswick, NJ 08901, USA.

出版信息

NAR Cancer. 2022 Jul 13;4(3):zcac021. doi: 10.1093/narcan/zcac021. eCollection 2022 Sep.

Abstract

SET domain-containing protein 4 (SETD4) is a member of a unique class of protein lysine methyltransferases. Here, we introduce the basic features of SETD4 and summarize the key findings from recent studies with emphases on its roles in tissue development and tumorigenesis, and its methylation substrates. SETD4 is expressed in stem/progenitor cells. Ablation of Setd4 cells impedes the repopulation of acinar cells after pancreatic injury. deletion in mice promotes the recovery of radiation-induced bone marrow (BM) failure by boosting the function of BM niche, facilitates the generation of endothelial cells and neovascularization of capillary vessels in the heart, enhances the proliferation of BM mesenchymal stem cells and disrupts the TLR4 signaling in BM-derived macrophages. SETD4 expression is also associated with the maintenance of quiescent breast cancer stem cells. While mouse knockout delays radiation-induced T-lymphoma formation, elevated SETD4 expression has been observed in some proliferative cancer cells and is associated with a pro-survival potential. Oncogenic fusions of SETD4 have also been identified in cancer, albeit rare. In addition, SETD4 methylates lysine-570 in the C-terminal globular domain of KU70, which enables KU70 translocation to cytoplasm to suppress apoptosis.

摘要

含SET结构域蛋白4(SETD4)是一类独特的蛋白质赖氨酸甲基转移酶中的成员。在此,我们介绍SETD4的基本特征,并总结近期研究的关键发现,重点关注其在组织发育和肿瘤发生中的作用及其甲基化底物。SETD4在干/祖细胞中表达。Setd4细胞的缺失会阻碍胰腺损伤后腺泡细胞的再生。小鼠中的缺失通过增强骨髓微环境的功能促进辐射诱导的骨髓(BM)衰竭的恢复,促进心脏中内皮细胞的生成和毛细血管的新生血管形成,增强BM间充质干细胞的增殖并破坏BM来源巨噬细胞中的TLR4信号传导。SETD4的表达还与静止乳腺癌干细胞的维持有关。虽然小鼠基因敲除会延迟辐射诱导的T淋巴瘤形成,但在一些增殖性癌细胞中观察到SETD4表达升高,并且与促生存潜力相关。在癌症中也鉴定出了SETD4的致癌融合体,尽管很罕见。此外,SETD4使KU70 C末端球状结构域中的赖氨酸-570甲基化,这使得KU70易位到细胞质中以抑制细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e449/9277757/5263599bee23/zcac021fig1.jpg

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