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缺乏RecQ解旋酶的人类疾病。

Human diseases deficient in RecQ helicases.

作者信息

Harrigan J A, Bohr V A

机构信息

Laboratory of Molecular Gerontology, National Institute on Aging, NIH, 5600 Nathan Shock Drive, Baltimore, MD 21224, USA.

出版信息

Biochimie. 2003 Nov;85(11):1185-93. doi: 10.1016/j.biochi.2003.10.006.

Abstract

RecQ helicases are conserved from bacteria to man. Mutations in three of the human RecQ family members give rise to genetic disorders characterized by genomic instability and a predisposition to cancer. RecQ helicases are therefore caretakers of the genome, and although they do not directly regulate tumorigenesis, they influence stability and the rate of accumulation of genetic alterations, which in turn, result in tumorigenesis. Maintenance of genome stability by RecQ helicases likely involves their participation in DNA replication, recombination, and repair pathways.

摘要

RecQ解旋酶从细菌到人类都是保守的。人类RecQ家族的三个成员发生突变会导致以基因组不稳定和易患癌症为特征的遗传疾病。因此,RecQ解旋酶是基因组的守护者,虽然它们不直接调节肿瘤发生,但它们会影响基因组改变的稳定性和积累速率,进而导致肿瘤发生。RecQ解旋酶对基因组稳定性的维持可能涉及其参与DNA复制、重组和修复途径。

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