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Noxa,一种仅含BH3结构域的Bcl-2家族成员,是p53诱导凋亡的潜在介导因子。

Noxa, a BH3-only member of the Bcl-2 family and candidate mediator of p53-induced apoptosis.

作者信息

Oda E, Ohki R, Murasawa H, Nemoto J, Shibue T, Yamashita T, Tokino T, Taniguchi T, Tanaka N

机构信息

Department of Immunology, Graduate School of Medicine and Faculty of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

Science. 2000 May 12;288(5468):1053-8. doi: 10.1126/science.288.5468.1053.

Abstract

A critical function of tumor suppressor p53 is the induction of apoptosis in cells exposed to noxious stresses. We report a previously unidentified pro-apoptotic gene, Noxa. Expression of Noxa induction in primary mouse cells exposed to x-ray irradiation was dependent on p53. Noxa encodes a Bcl-2 homology 3 (BH3)-only member of the Bcl-2 family of proteins; this member contains the BH3 region but not other BH domains. When ectopically expressed, Noxa underwent BH3 motif-dependent localization to mitochondria and interacted with anti-apoptotic Bcl-2 family members, resulting in the activation of caspase-9. We also demonstrate that blocking the endogenous Noxa induction results in the suppression of apoptosis. Noxa may thus represent a mediator of p53-dependent apoptosis.

摘要

肿瘤抑制因子p53的一项关键功能是在遭受有害应激的细胞中诱导细胞凋亡。我们报告了一个此前未被鉴定的促凋亡基因Noxa。在受到X射线照射的原代小鼠细胞中,Noxa的诱导表达依赖于p53。Noxa编码一种仅含Bcl-2同源结构域3(BH3)的Bcl-2家族蛋白;该成员含有BH3区域,但不含其他BH结构域。当异位表达时,Noxa会通过依赖BH3基序的方式定位于线粒体,并与抗凋亡的Bcl-2家族成员相互作用,从而激活caspase-9。我们还证明,阻断内源性Noxa的诱导会导致细胞凋亡受到抑制。因此,Noxa可能是p53依赖性细胞凋亡的一种介质。

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