7221名旧秩序阿米什人的外显子变异及其临床影响。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Braxton D Mitchell, Ebuka Onyenobi, Joshua P Lewis, Brady Gaynor, James A Perry, Kristin Maloney, Jeffrey R O'Connell, Jessica Tiner, Amber L Beitelshees, Cristopher V Van Hout, Patrick F McArdle, Huichun Xu, Erik G Puffenberger, Karlla W Brigatti, Melanie Daue, Hilary B Whitlatch, Anna Alkelai, Alejandro A Schäffer, John Overton, Elizabeth A Streeten, Toni I Pollin, Alan R Shuldiner
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引用次数: 0

摘要

宾夕法尼亚州兰开斯特县的阿米什人多年来一直是基因研究的焦点,因为它的人口统计历史和独特的基因构成,包括历史瓶颈事件和随后的遗传漂变,导致遗传多样性显著减少,一些变异的频率增加,这些变异极大地影响了社区的健康。为了描述阿米什人基因组的编码差异,我们对7221名成年社区成员的外显子组进行了测序,并在本报告中对比了阿米什人和来自英国生物银行的欧洲人的遗传多样性。7221名阿米什人的外显子组序列所包含的变异数量仅为相同数量的UKB参与者的14%。这种减少的基因多样性具有重要的临床意义。我们从ClinVar和群体特异性遗传筛选小组中鉴定了致病性(P)和可能致病性(LP)变异,发现阿米什人中的大多数变异都是高度富集的,导致5.2%的阿米什人为隐性P/LP变异纯合,25.6%为至少一种显性P/LP变异杂合。在我们样本中的2141对阿米什夫妇中,43.6%的人至少有一方是P/LP显性变异的杂合,24.3%的夫妇是常染色体隐性遗传病携带者,这意味着他们的每个孩子都有25%的风险遗传该变异的两个拷贝。在其他创始人社区的基因发现工作可能会发现影响这些社区健康的不同的P(和有益的)变异,对所有人类健康都有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exonic Variation and Its Clinical Impact in 7221 Old Order Amish.

The Amish of Lancaster County, PA has been the focus of genetic studies for many years due to its demographic history and unique genetic makeup that includes a historical bottleneck event and subsequent genetic drift, resulting in a marked decrease in genetic diversity and increased frequency of some variants that have substantially shaped the health of the community. To characterize the coding variation in the Amish genome, we sequenced the exomes of 7221 adult community members, and in this report, we contrast genetic diversity between the Amish and Europeans from the UK Biobank. Exome sequences of 7221 Amish contained only 14% as many variants as the same number of UKB participants. This reduced genetic diversity has substantial clinical implications. We identified pathogenic (P) and likely pathogenic (LP) variants from ClinVar and a population-specific genetic screening panel and found that most of the variants present in the Amish were highly enriched, resulting in 5.2% of Amish individuals being homozygous for a recessive P/LP variant and 25.6% being heterozygous for at least one dominant P/LP variant. In 43.6% of the 2141 Amish spouse-pairs in our sample, at least one spouse was heterozygous for a P/LP dominant variant, and 24.3% of couples were autosomal recessive disease carrier couples, meaning that each of their children was at ~25% risk of inheriting two copies of that variant. Gene discovery efforts in other founder communities will likely uncover distinct P (and beneficial) variants impacting the health of these communities, with implications for all of human health.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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