Suppr超能文献

脆性 X 完全突变扩增受前突变携带者中一个或多个 AGG 中断的抑制。

Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers.

机构信息

Department of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, New York, USA.

Asuragen Inc., Austin, Texas, USA.

出版信息

Genet Med. 2015 May;17(5):358-64. doi: 10.1038/gim.2014.106. Epub 2014 Sep 11.

Abstract

PURPOSE

Fragile X CGG repeat alleles often contain one or more AGG interruptions that influence allele stability and risk of a full mutation transmission from parent to child. We have examined transmissions of maternal and paternal alleles with 45-90 repeats to quantify the effect of AGG interruptions on fragile X repeat instability.

METHODS

A novel FMR1 polymerase chain reaction assay was used to determine CGG repeat length and AGG interruptions for 1,040 alleles from 705 families.

RESULTS

We grouped transmissions into nine categories of five repeats by parental size and found that in every size category, alleles with no AGGs had the greatest risk for instability. For maternal alleles <75 repeats, 89% (24/27) that expanded to a full mutation had no AGGs. Two contractions in maternal transmission were accompanied by loss of AGGs, suggesting a mechanism for generating alleles that lack AGG interruptions. Maternal age was examined as a factor in full mutation expansions using prenatal samples to minimize ascertainment bias, and a possible effect was observed though it was not statistically significant (P = 0.06).

CONCLUSION

These results strengthen the association of AGG repeats with CGG repeat stability and provide more accurate risk estimates of full mutation expansions for women with 45-90 repeat alleles.

摘要

目的

脆性 X CGG 重复等位基因通常含有一个或多个 AGG 中断,这会影响等位基因的稳定性和从父母传递至子女的完全突变的风险。我们已经研究了 45-90 个重复的母系和父系等位基因的传递,以量化 AGG 中断对脆性 X 重复不稳定的影响。

方法

我们使用一种新型的 FMR1 聚合酶链反应检测方法,对来自 705 个家庭的 1040 个等位基因的 CGG 重复长度和 AGG 中断进行了测定。

结果

我们根据亲本大小将传递分为五类五个重复的九个类别,并发现在每个大小类别中,没有 AGG 的等位基因最不稳定。对于小于 75 个重复的母系等位基因,89%(24/27)扩展为完全突变的等位基因没有 AGG。母系传递中的两次收缩伴随着 AGG 的丢失,表明了一种产生缺乏 AGG 中断的等位基因的机制。使用产前样本作为一种因素来检查母体年龄对完全突变扩展的影响,以尽量减少确定偏差,尽管这不是统计学上显著的(P=0.06),但还是观察到了可能的影响。

结论

这些结果加强了 AGG 重复与 CGG 重复稳定性的关联,并为 45-90 个重复等位基因的女性提供了更准确的完全突变扩展风险估计。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验