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对我们在体细胞哺乳动物细胞中对辐射诱导的 DNA 双链断裂修复的理解的历史反思;连接过去与现在。

A historical reflection on our understanding of radiation-induced DNA double strand break repair in somatic mammalian cells; interfacing the past with the present.

机构信息

a Education and Research Support Center , Gunma University Graduate School of Medicine , Gunma , Maebashi , Japan.

b Genome Damage and Stability Centre, School of Life Sciences , University of Sussex , Brighton , UK.

出版信息

Int J Radiat Biol. 2019 Jul;95(7):945-956. doi: 10.1080/09553002.2018.1564083. Epub 2019 Jan 17.

Abstract

The International Journal of Radiation Biology (IJRB) is celebrating 60 years of publishing in 2019. IJRB has made an enormous contribution to publishing papers that have enhanced our understanding of the DNA damage response (DDR) activated following exposure to ionizing radiation (IR). The IR-induced DDR field has a rich history but many outstanding papers pass unread by young scientists overwhelmed by the current literature. We provide a historical reflection on key advances in the DDR field and interface them with current knowledge. DNA double strand breaks (DSBs) were identified as the major biological lesion induced by IR. But early studies on cells from IR-sensitive ataxia telangiectasia patients showed that DSB repair was not sufficient to prevent IR hypersensitivity. Subsequently, the ATM-dependent signal transduction process was revealed, with the breadth of the response being slowly unearthed. Early studies demonstrated at least two processes of DSB repair and revealed that mis-repair causes translocation formation. Recent studies, however, are unraveling more complexity in the repair process, including the specific processing of DSBs within transcriptionally active regions, and the significance of the chromatin environment. Despite the quality of these early and current studies, many questions remain to be addressed.

摘要

《国际放射生物学杂志》(IJRB)于 2019 年庆祝创刊 60 周年。IJRB 为发表增强我们对电离辐射(IR)暴露后 DNA 损伤反应(DDR)理解的论文做出了巨大贡献。IR 诱导的 DDR 领域历史悠久,但许多杰出的论文被当前文献淹没的年轻科学家忽视了。我们对 DDR 领域的关键进展进行了历史反思,并将其与当前的知识联系起来。DNA 双链断裂(DSBs)被确定为 IR 诱导的主要生物学损伤。但对来自辐射敏感共济失调毛细血管扩张症患者的细胞的早期研究表明,DSB 修复不足以防止 IR 超敏反应。随后,揭示了 ATM 依赖性信号转导过程,其反应的广度逐渐被揭示。早期研究表明至少有两种 DSB 修复过程,并揭示了错误修复会导致易位形成。然而,最近的研究正在揭示修复过程中的更多复杂性,包括转录活跃区域内 DSB 的特定处理,以及染色质环境的意义。尽管这些早期和当前的研究质量很高,但仍有许多问题有待解决。

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