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微注射部分纯化的蛋白因子可特异性修复着色性干皮病细胞A组中的DNA损伤。

Microinjection of partially purified protein factor restores DNA damage specifically in group A of xeroderma pigmentosum cells.

作者信息

Yamaizumi M, Sugano T, Asahina H, Okada Y, Uchida T

出版信息

Proc Natl Acad Sci U S A. 1986 Mar;83(5):1476-9. doi: 10.1073/pnas.83.5.1476.

Abstract

Microinjection of cell extracts prepared from both human placenta and HeLa cells into xeroderma pigmentosum (XP) cells of complementation group A restores unscheduled DNA synthesis (UDS) in these cells after UV irradiation [de Jonge, A., Vermeulen, W., Klein, B. & Hoeijmakers, J. (1983) EMBO J. 2, 637-641]. These cells also showed normal resistance to UV irradiation. The half-life of the factors in the cell extracts corresponding to the UDS activity (factor A) was 14 hr in XP cells of group A, and the maximal level of UDS was exerted 2 hr after microinjection. The factors were sensitive to protease treatment but not to RNase treatment and were found to be approximately equal to 160 and approximately equal to 90 kDa by gel filtration. These two fractions of the factor(s) acted specifically in XP cells of complementation group A among complementation groups A, B, C, D, F, G, and probably E and H.

摘要

将从人胎盘和HeLa细胞制备的细胞提取物显微注射到互补组A的着色性干皮病(XP)细胞中,可在紫外线照射后恢复这些细胞中的非预定DNA合成(UDS)[de Jonge, A., Vermeulen, W., Klein, B. & Hoeijmakers, J. (1983) EMBO J. 2, 637 - 641]。这些细胞对紫外线照射也表现出正常的抗性。在A组XP细胞中,与UDS活性相对应的细胞提取物中的因子(因子A)的半衰期为14小时,显微注射后2小时达到UDS的最大水平。这些因子对蛋白酶处理敏感,但对核糖核酸酶处理不敏感,通过凝胶过滤发现其分子量分别约为160 kDa和约90 kDa。在互补组A、B、C、D、F、G以及可能的E和H中,这两个因子组分在互补组A的XP细胞中具有特异性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a63/323099/0d3d60b190bb/pnas00309-0316-a.jpg

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