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缺乏依赖于 DNA 的蛋白激酶(DNA-PKcs)的催化亚基伴随着 CK2α'水平的升高。

Lack of the catalytic subunit of DNA-dependent protein kinase (DNA-PKcs) is accompanied by increased CK2α' levels.

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, 5230 Odense, Denmark.

出版信息

Mol Cell Biochem. 2011 Oct;356(1-2):139-47. doi: 10.1007/s11010-011-0954-7. Epub 2011 Jul 13.

Abstract

DNA-PKcs is the catalytic subunit of DNA-dependent protein kinase, an enzyme necessary for non-homologous end-joining (NHEJ) and hence repair of DNA double strand breaks. Characterization of two isogenic cell lines, M059K and M059J, which are DNA-PKcs-proficient and -deficient, respectively, revealed that lack of DNA-PKcs is accompanied by an increase in the protein level of one of the catalytic isozymes of protein kinase CK2, i.e., CK2α' and a concomitant increase in CK2 activity. The increase was also detectable at the mRNA level as measured by quantitative real time PCR. However, no increase at the DNA level was observed either by comparative PCR or fluorescent in situ hybridization indicating that gene amplification is not involved. Interestingly, only CK2α' was increased and not the other two subunits of CK2, i.e., CK2β or CK2α. In addition, the increase in CK2α' protein level was also observed in a DNA-PKcs-deficient mouse cell line.

摘要

DNA-PKcs 是 DNA 依赖性蛋白激酶的催化亚基,该酶对于非同源末端连接(NHEJ)和双链 DNA 断裂修复是必需的。对两种同基因细胞系 M059K 和 M059J 的特征分析表明,分别缺乏 DNA-PKcs 会导致蛋白激酶 CK2 的一个催化同工酶,即 CK2α'的蛋白水平增加,同时 CK2 活性增加。通过定量实时 PCR 检测到这种增加也可以在 mRNA 水平上检测到。然而,通过比较 PCR 或荧光原位杂交均未观察到 DNA 水平的增加,表明基因扩增不参与其中。有趣的是,只有 CK2α'增加,而 CK2 的其他两个亚基,即 CK2β 或 CK2α 没有增加。此外,在缺乏 DNA-PKcs 的小鼠细胞系中也观察到 CK2α'蛋白水平的增加。

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