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DNA链断裂修复与人类遗传疾病。

DNA strand break repair and human genetic disease.

作者信息

McKinnon Peter J, Caldecott Keith W

机构信息

Department of Genetics and Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

出版信息

Annu Rev Genomics Hum Genet. 2007;8:37-55. doi: 10.1146/annurev.genom.7.080505.115648.

Abstract

Each day tens of thousands of DNA single-strand breaks (SSBs) arise in every cell from the attack of deoxyribose and DNA bases by reactive oxygen species and other electrophilic molecules. DNA double-strand breaks (DSBs) also arise, albeit at a much lower frequency, from similar attacks and from the encounter of unrepaired SSBs and possibly other DNA structures by DNA replication forks. DSBs are also created during normal development of the immune system. Defects in the cellular response to DNA strand breaks underpin many human diseases, including disorders associated with cancer predisposition, immune dysfunction, radiosensitivity, and neurodegeneration. Here we provide an overview of the genetic diseases associated with defects in the repair/response to DNA strand breaks.

摘要

每天,活性氧和其他亲电分子对脱氧核糖和DNA碱基的攻击会导致每个细胞中出现数以万计的DNA单链断裂(SSB)。DNA双链断裂(DSB)也会出现,尽管频率要低得多,其来源包括类似的攻击、未修复的SSB与DNA复制叉相遇以及可能与其他DNA结构相遇。在免疫系统的正常发育过程中也会产生DSB。细胞对DNA链断裂反应的缺陷是许多人类疾病的基础,包括与癌症易感性、免疫功能障碍、放射敏感性和神经退行性变相关的疾病。在这里,我们概述了与DNA链断裂修复/反应缺陷相关的遗传疾病。

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