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质子微束辐照造成的局部DNA损伤可诱导哺乳动物细胞中聚(ADP-核糖)的合成。

Local DNA damage by proton microbeam irradiation induces poly(ADP-ribose) synthesis in mammalian cells.

作者信息

Tartier Laurence, Spenlehauer Catherine, Newman Heidi C, Folkard Melvyn, Prise Kevin M, Michael Barry D, Ménissier-de Murcia Josiane, de Murcia Gilbert

机构信息

Unité 9003 du CNRS, Laboratoire Conventionné avec le Commissariat à l'Energie Atomique, Ecole Supérieure de Biotechnologie de Strasbourg, Boulevard Sebastien Brant, BP 10413, F-67412 Illkirch-Graffenstaden, France.

出版信息

Mutagenesis. 2003 Sep;18(5):411-6. doi: 10.1093/mutage/geg015.

Abstract

Cellular recovery from ionizing radiation (IR)-induced damage involves poly(ADP-ribose) polymerase (PARP-1 and PARP-2) activity, resulting in the induction of a signalling network responsible for the maintenance of genomic integrity. In the present work, a charged particle microbeam delivering 3.2 MeV protons from a Van de Graaff accelerator has been used to locally irradiate mammalian cells. We show the immediate response of PARPs to local irradiation, concomitant with the recruitment of ATM and Rad51 at sites of DNA damage, both proteins being involved in DNA strand break repair. We found a co-localization but no connection between two DNA damage-dependent post-translational modifications, namely poly(ADP-ribosyl)ation of nuclear proteins and phosphorylation of histone H2AX. Both of them, however, should be considered and used as bona fide immediate sensitive markers of IR damage in living cells. This technique thus provides a powerful approach aimed at understanding the interactions between the signals originating from sites of DNA damage and the subsequent activation of DNA strand break repair mechanisms

摘要

细胞从电离辐射(IR)诱导的损伤中恢复涉及聚(ADP - 核糖)聚合酶(PARP - 1和PARP - 2)的活性,从而导致负责维持基因组完整性的信号网络的诱导。在本研究中,使用了一台从范德格拉夫加速器发射3.2 MeV质子的带电粒子微束对哺乳动物细胞进行局部照射。我们展示了PARP对局部照射的即时反应,同时伴随ATM和Rad51在DNA损伤位点的募集,这两种蛋白质都参与DNA链断裂修复。我们发现两种依赖于DNA损伤的翻译后修饰之间存在共定位但无关联,即核蛋白的聚(ADP - 核糖)基化和组蛋白H2AX的磷酸化。然而,这两者都应被视为并用作活细胞中IR损伤的真正即时敏感标志物。因此,这项技术提供了一种强大的方法,旨在理解源自DNA损伤位点的信号与随后DNA链断裂修复机制激活之间的相互作用。

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