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在G1/S期边界,电离辐射产生的DNA损伤的组成性或诱导性修复不需要TP53。

TP53 is not required for the constitutive or induced repair of DNA damage produced by ionizing radiation at the G1/S-phase border.

作者信息

Whisnant-Hurst N, Leadon S A

机构信息

Department of Radiation Oncology, University of North Carolina at Chapel Hill, 27599-7512, USA.

出版信息

Radiat Res. 1999 Mar;151(3):263-9.

Abstract

We have previously described a novel DNA repair response that is induced in cells irradiated with ionizing radiation at the G1/S-phase border and is characterized by the formation of very long repair patches (VLRP) containing at least 150 nucleotides. In the current study, we examined whether there is a requirement for TP53 in this induced repair process. We find that in normal cells, the endogenous levels of TP53 are elevated at the G1/S-phase border, and that these levels are not further increased after irradiation with 5 Gy. In cells expressing the E6 oncoprotein of human papillomavirus, which inactivates TP53 function, there is a greatly accentuated induction of the VLRP that nearly masks the constitutive repair response. Incubation of cells in the presence of cycloheximide, which inhibits the induced repair, reveals the presence of the constitutive repair patches. All cells examined continue to replicate their DNA after exposure to ionizing radiation. In contrast, cells irradiated with UV radiation at the G1/S-phase border show an induction of TP53 protein and halt DNA synthesis, but do not induce the VLRP. Our results show that TP53 is not required for the constitutive or induced repair of DNA damage induced by ionizing radiation. In addition, these results suggest that TP53 may suppress the formation of VLRP and that the progression of cells through S phase after exposure to ionizing radiation signals the induced repair response.

摘要

我们之前描述过一种新的DNA修复反应,它在处于G1/S期边界的细胞受到电离辐射后被诱导产生,其特征是形成包含至少150个核苷酸的非常长的修复补丁(VLRP)。在当前的研究中,我们检测了在这种诱导的修复过程中是否需要TP53。我们发现,在正常细胞中,TP53的内源性水平在G1/S期边界处升高,并且在用5 Gy辐射后这些水平不会进一步增加。在表达人乳头瘤病毒E6癌蛋白(该蛋白会使TP53功能失活)的细胞中,VLRP的诱导显著增强,几乎掩盖了组成型修复反应。在存在抑制诱导修复的环己酰亚胺的情况下培养细胞,揭示了组成型修复补丁的存在。所有检测的细胞在暴露于电离辐射后继续复制其DNA。相比之下,在G1/S期边界受到紫外线辐射的细胞会诱导TP53蛋白表达并停止DNA合成,但不会诱导VLRP。我们的结果表明,TP53对于电离辐射诱导的DNA损伤的组成型或诱导型修复不是必需的。此外,这些结果表明TP53可能会抑制VLRP的形成,并且细胞在暴露于电离辐射后通过S期的进程标志着诱导的修复反应。

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