Suppr超能文献

共济失调毛细血管扩张症细胞在γ射线照射后(ADP-核糖)n和DNA合成水平异常

Unusual levels of (ADP-ribose)n and DNA synthesis in ataxia telangiectasia cells following gamma-ray irradiation.

作者信息

Edwards M J, Taylor A M

出版信息

Nature. 1980 Oct 23;287(5784):745-7. doi: 10.1038/287745a0.

Abstract

Poly (ADP-ribose) polymerase is a eukaryotic chromosomal enzyme which utilizes the ADP-ribose moiety of NAD to synthesize the nucleic acid homopolymer (ADP-ribose)n (ref. 1). The precise function of (ADP-ribose)n has not been fully established although it does covalently modify chromosomal proteins by ADP-ribosylation. Here we demonstrate that gamma-ray irradiation of lymphoblastoid cells from normal subjects results in depressed DNA synthesis and increased (ADP-ribose)n synthesis. Irradiation of lymphoblastoid cells from patients with the autosomal recessive disease ataxia telangiectasia (AT), however, failed to depress DNA synthesis and did not elevate (ADP-ribose)n levels. We have confirmed that (ADP-ribose)n is synthesized in response to DNA damage and we propose that this polymer may function in the recovery from DNA damage by suppressing DNA synthesis.

摘要

聚(ADP - 核糖)聚合酶是一种真核染色体酶,它利用NAD的ADP - 核糖部分来合成核酸同聚物(ADP - 核糖)n(参考文献1)。尽管(ADP - 核糖)n确实通过ADP - 核糖基化共价修饰染色体蛋白,但其确切功能尚未完全明确。在此我们证明,对正常受试者的淋巴母细胞进行γ射线照射会导致DNA合成受抑以及(ADP - 核糖)n合成增加。然而,对患有常染色体隐性疾病共济失调毛细血管扩张症(AT)患者的淋巴母细胞进行照射,未能抑制DNA合成,也未提高(ADP - 核糖)n水平。我们已证实(ADP - 核糖)n是响应DNA损伤而合成的,并且我们提出这种聚合物可能通过抑制DNA合成在DNA损伤修复中发挥作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验