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DNA 修复缺陷小鼠模型中的单倍不足:外显率的修饰因子。

Haploinsufficiency in mouse models of DNA repair deficiency: modifiers of penetrance.

机构信息

Department of Nutrition and Food Science, Wayne State University, Detroit, MI 48201, USA.

出版信息

Cell Mol Life Sci. 2012 Mar;69(5):727-40. doi: 10.1007/s00018-011-0839-7. Epub 2011 Sep 28.

Abstract

Mouse models of DNA repair deficiency are useful tools for determining susceptibility to disease. Cancer predisposition and premature aging are commonly impacted by deficiencies in DNA repair, presumably as a function of reduced genomic fitness. In this review, a comprehensive analysis of all DNA repair mutant mouse models has been completed in order to assess the importance of haploinsufficiency for these genes. This analysis brings to light a clear role for haploinsufficiency in disease predisposition. Unfortunately, much of the data on heterozygous models are buried or underinvestigated. In light of a better understanding that the role of DNA repair haploinsufficiency may play in penetrance of other oncogenic or disease causing factors, it may be in the interest of human health and disease prevention to further investigate the phenotypes in many of these mouse models.

摘要

DNA 修复缺陷的小鼠模型是确定疾病易感性的有用工具。癌症易感性和早衰通常受到 DNA 修复缺陷的影响,这可能是由于基因组适应性降低所致。在这篇综述中,我们全面分析了所有的 DNA 修复突变体小鼠模型,以评估这些基因的杂合不足的重要性。该分析揭示了杂合不足在疾病易感性中的重要作用。不幸的是,许多关于杂合模型的数据被埋没或研究不足。鉴于更好地理解 DNA 修复杂合不足可能在其他致癌或致病因素的外显率中发挥的作用,进一步研究这些小鼠模型中的许多表型可能符合人类健康和疾病预防的利益。

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