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小鼠中脆性X综合征重复序列的不稳定性:年龄、饮食以及影响DNA复制、重组和修复能力的基因突变的作用。

Instability of the fragile X syndrome repeat in mice: the effect of age, diet and mutations in genes that affect DNA replication, recombination and repair proficiency.

作者信息

Fleming K, Riser D K, Kumari D, Usdin K

机构信息

Section on Genomic Structure and Function, Laboratory of Molecular and Cellular Biology, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0830, USA.

出版信息

Cytogenet Genome Res. 2003;100(1-4):140-6. doi: 10.1159/000072848.

Abstract

Repeat expansion diseases such as fragile X syndrome (FXS) result from increases in the size of a specific tandem repeat array. In addition to large expansions, small changes in repeat number and deletions are frequently seen in FXS pedigrees. No mouse model accurately recapitulates all aspects of this instability, particularly the occurrence of large expansions. This may be due to differences between mice and humans in CIS and/or TRANS-acting factors that affect repeat stability. The identification of such factors may help reveal the expansion mechanism and allow the development of suitable animal models for these disorders. We have examined the effect of age, dietary folate, and mutations in the Werner's syndrome helicase (WRN) and TRP53 genes on FXS repeat instability in mice. WRN facilitates replication of the FXS repeat and enhances Okazaki fragment processing, thereby reducing the incidence of processes that have been suggested to lead to expansion. p53 is a protein involved in DNA damage surveillance and repair. We find two types of repeat instability in these mice, small changes in repeat number that are seen at frequencies approaching 100%, and large deletions which occur at a frequency of about 10%. The frequency of these events was independent of WRN, p53, parental age, or folate levels. The large deletions occur at the same frequency in mice homozygous and heterozygous for the repeat suggesting that they are not the result of an interallelic recombination event. In addition, no evidence of large expansions was seen. Our data thus show that the absence of repeat expansions in mice is not due to a more efficient WRN protein or p53-mediated error correction mechanism, and suggest that these proteins, or the pathways in which they are active, may not be involved in expansion in humans either. Moreover, the fact that contractions occur in the absence of expansions suggests that these processes occur by different mechanisms.

摘要

诸如脆性X综合征(FXS)等重复序列扩增疾病是由特定串联重复序列阵列大小的增加所致。除了大的扩增外,FXS家系中还经常出现重复次数的小变化和缺失。没有小鼠模型能够准确地概括这种不稳定性的所有方面,特别是大扩增的发生情况。这可能是由于小鼠和人类在影响重复序列稳定性的顺式和/或反式作用因子方面存在差异。鉴定这些因子可能有助于揭示扩增机制,并为这些疾病开发合适的动物模型。我们研究了年龄、饮食中的叶酸以及Werner综合征解旋酶(WRN)和TRP53基因突变对小鼠FXS重复序列不稳定性的影响。WRN促进FXS重复序列的复制并增强冈崎片段的加工,从而降低了被认为会导致扩增的过程的发生率。p53是一种参与DNA损伤监测和修复的蛋白质。我们在这些小鼠中发现了两种类型的重复序列不稳定性,重复次数的小变化出现频率接近100%,大缺失的发生频率约为10%。这些事件的频率与WRN、p53、亲本年龄或叶酸水平无关。纯合和杂合重复序列的小鼠中,大缺失的发生频率相同,这表明它们不是等位基因间重组事件的结果。此外,未观察到大扩增的证据。因此,我们的数据表明,小鼠中不存在重复序列扩增不是由于WRN蛋白或p53介导的纠错机制更有效,并表明这些蛋白质或它们所参与的途径可能也不参与人类的扩增过程。此外,在没有扩增的情况下出现收缩这一事实表明,这些过程是通过不同的机制发生的。

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