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DUB-1,一种具有生长抑制活性的去泛素化酶。

DUB-1, a deubiquitinating enzyme with growth-suppressing activity.

作者信息

Zhu Y, Carroll M, Papa F R, Hochstrasser M, D'Andrea A D

机构信息

Division of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3275-9. doi: 10.1073/pnas.93.8.3275.

Abstract

Cytokines regulate cell growth by inducing the expression of specific target genes. Using the differential display method, we have cloned a cytokine-inducible immediate early gene, DUB-1 (for deubiquitinating enzyme). DUB-1 is related to members of the UBP superfamily of deubiquitinating enzymes, which includes the oncoprotein Tre-2. A glutathione S-transferase-DUB-1 fusion protein cleaved ubiquitin from a ubiquitin-beta-galactosidase protein. When a conserved cysteine residue of DUB-1, required for ubiquitin-specific thiol protease activity, was mutated to serine (C60S), deubiquitinating activity was abolished. Continuous expression of DUB-1 from a steroid-inducible promoter induced growth arrest in the G1 phase of the cell cycle. Cells arrested by DUB-1 expression remained viable and resumed proliferation upon steroid withdrawal. Our results suggest that DUB-1 regulates cellular growth by modulating either the ubiquitin-dependent proteolysis or the ubiquitination state of an unknown growth regulatory factor(s).

摘要

细胞因子通过诱导特定靶基因的表达来调节细胞生长。利用差异显示法,我们克隆了一个细胞因子诱导的即刻早期基因DUB-1(去泛素化酶)。DUB-1与去泛素化酶的UBP超家族成员相关,该家族包括癌蛋白Tre-2。谷胱甘肽S-转移酶-DUB-1融合蛋白从泛素-β-半乳糖苷酶蛋白上切割下泛素。当DUB-1中泛素特异性硫醇蛋白酶活性所需的保守半胱氨酸残基突变为丝氨酸(C60S)时,去泛素化活性丧失。从类固醇诱导型启动子持续表达DUB-1会诱导细胞周期G1期的生长停滞。因DUB-1表达而停滞的细胞仍保持活力,并在撤除类固醇后恢复增殖。我们的结果表明,DUB-1通过调节泛素依赖性蛋白水解或未知生长调节因子的泛素化状态来调节细胞生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cc/39596/cfd9930a586f/pnas01515-0127-a.jpg

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