带有 rs41524547-G 的扩展单倍型定义了 SCA10 的祖先起源。

IF 3.1 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Karen N McFarland, Anjana Tiwari, Vera Hashem, Linwei Zhang, Desmond Zeng, Justin Vincent, Maria J Arredondo, Kristy L Johnson, Shi Rui Gan, Ichiro Yabe, Laurits Skov, Astrid Rasmussen, Tetsuo Ashizawa
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引用次数: 0

摘要

脊髓小脑共济失调 10 型(SCA10)是一种罕见的常染色体显性共济失调,由 ATXN10 中 (ATTCT)n 重复序列的大量扩增引起。SCA10 在美洲原住民和亚洲人中被描述,这促使人们寻找扩增的单倍型,以确认扩增事件的共同祖源。我们队列中的所有 SCA10 扩增患者都有一个单倍型,其 5'- 端由位于 SCA10 扩增上游 ~35 kb 的 rs41524547 小等位基因定义。耐人寻味的是,rs41524547 位于 miRNA 基因 MIR4762 中,在其 DROSHA 分裂位点内,刚好位于 mir4792-5p 种子序列之外。rs41524547-G 的全球频率低于 5%,几乎只出现在美洲和东亚--这一地理分布反映了已报道的 SCA10 病例。我们从 1000 基因组/国际基因组样本资源和我们自己的普通人群样本中鉴定出了 rs41524547-G(+) DNA,并在这些样本中鉴定出了高达 25% 的 SCA10 重复扩增。这些 SCA10 扩增的低渗透性可能是由于样本采集时年龄较小(发病前)、重复大小较小、重复单位纯度较高或 miR4762-5p 功能被破坏。我们的结论是,rs41524547-G 是 SCA10 最稳健的高危 SNP 等位基因,有助于在群体遗传学研究中筛选 SCA10 扩增,并为 SCA10 扩增的单一史前起源提供了迄今为止最有力的证据,即在个体穿越白令陆桥迁移到美洲之前或期间的某个时期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extended haplotype with rs41524547-G defines the ancestral origin of SCA10.

Spinocerebellar ataxia type 10 (SCA10) is a rare autosomal dominant ataxia caused by a large expansion of the (ATTCT)n repeat in ATXN10. SCA10 was described in Native American and Asian individuals which prompted a search for an expanded haplotype to confirm a common ancestral origin for the expansion event. All patients with SCA10 expansions in our cohort share a single haplotype defined at the 5'-end by the minor allele of rs41524547, located ~35 kb upstream of the SCA10 expansion. Intriguingly, rs41524547 is located within the miRNA gene, MIR4762, within its DROSHA cleavage site and just outside the seed sequence for mir4792-5p. The world-wide frequency of rs41524547-G is less than 5% and found almost exclusively in the Americas and East Asia-a geographic distribution that mirrors reported SCA10 cases. We identified rs41524547-G(+) DNA from the 1000 Genomes/International Genome Sample Resource and our own general population samples and identified SCA10 repeat expansions in up to 25% of these samples. The reduced penetrance of these SCA10 expansions may be explained by a young (pre-onset) age at sample collection, a small repeat size, purity of repeat units, or the disruption of miR4762-5p function. We conclude that rs41524547-G is the most robust at-risk SNP allele for SCA10, is useful for screening of SCA10 expansions in population genetics studies and provides the most compelling evidence to date for a single, prehistoric origin of SCA10 expansions sometime prior to or during the migration of individuals across the Bering Land Bridge into the Americas.

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来源期刊
Human molecular genetics
Human molecular genetics 生物-生化与分子生物学
CiteScore
6.90
自引率
2.90%
发文量
294
审稿时长
2-4 weeks
期刊介绍: Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. These include: the molecular basis of human genetic disease developmental genetics cancer genetics neurogenetics chromosome and genome structure and function therapy of genetic disease stem cells in human genetic disease and therapy, including the application of iPS cells genome-wide association studies mouse and other models of human diseases functional genomics computational genomics In addition, the journal also publishes research on other model systems for the analysis of genes, especially when there is an obvious relevance to human genetics.
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