Sallmyr A, Henriksson G, Fukushima S, Bredberg A
Department of Medical Microbiology, Lund University, Malmö University Hospital, S-205 02, Malmö, Sweden.
Biochim Biophys Acta. 2001 Apr 23;1538(2-3):305-12. doi: 10.1016/s0167-4889(01)00081-7.
DNA-dependent protein kinase (DNA-PK) has been shown to take part in cell cycle regulatory signal transduction and in the repair of X-ray-induced DNA double-strand breaks. Functional DNA-PK is furthermore needed for the generation of antigen specificity during lymphocyte maturation. The Ku86 subunit of DNA-PK has been reported to exist in human B lymphocytes in a truncated form capable of binding to broken DNA but lacking the ability to activate the kinase function of DNA-PK. In the present work the Ku70 and Ku86 dimer proteins in T and B lymphocytes from human blood donors were analysed by immunoblotting and were observed apparently to be of full length. Also, nuclear protein extracted from B and non-B lymphocytes displayed DNA-dependent kinase activity. However, a minor fraction of Ku86 in lymphocytes was observed to be truncated with a molecular mass of approx. 70 kDa.
DNA依赖性蛋白激酶(DNA-PK)已被证明参与细胞周期调节信号转导以及X射线诱导的DNA双链断裂的修复。此外,功能性DNA-PK是淋巴细胞成熟过程中产生抗原特异性所必需的。据报道,DNA-PK的Ku86亚基以截短形式存在于人类B淋巴细胞中,该截短形式能够与断裂的DNA结合,但缺乏激活DNA-PK激酶功能的能力。在本研究中,通过免疫印迹分析了来自人类献血者的T和B淋巴细胞中的Ku70和Ku86二聚体蛋白,观察到它们显然是全长的。此外,从B淋巴细胞和非B淋巴细胞中提取的核蛋白显示出DNA依赖性激酶活性。然而,观察到淋巴细胞中一小部分Ku86被截短,分子量约为70 kDa。