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撒丁岛的身高降低变异与矮身材选择

Height-reducing variants and selection for short stature in Sardinia.

作者信息

Zoledziewska Magdalena, Sidore Carlo, Chiang Charleston W K, Sanna Serena, Mulas Antonella, Steri Maristella, Busonero Fabio, Marcus Joseph H, Marongiu Michele, Maschio Andrea, Ortega Del Vecchyo Diego, Floris Matteo, Meloni Antonella, Delitala Alessandro, Concas Maria Pina, Murgia Federico, Biino Ginevra, Vaccargiu Simona, Nagaraja Ramaiah, Lohmueller Kirk E, Timpson Nicholas J, Soranzo Nicole, Tachmazidou Ioanna, Dedoussis George, Zeggini Eleftheria, Uzzau Sergio, Jones Chris, Lyons Robert, Angius Andrea, Abecasis Gonçalo R, Novembre John, Schlessinger David, Cucca Francesco

机构信息

Istituto di Ricerca Genetica e Biomedica, CNR, Monserrato, Cagliari, Italy.

Center for Statistical Genetics, Ann Arbor, University of Michigan, MI, USA.

出版信息

Nat Genet. 2015 Nov;47(11):1352-1356. doi: 10.1038/ng.3403. Epub 2015 Sep 14.

Abstract

We report sequencing-based whole-genome association analyses to evaluate the impact of rare and founder variants on stature in 6,307 individuals on the island of Sardinia. We identify two variants with large effects. One variant, which introduces a stop codon in the GHR gene, is relatively frequent in Sardinia (0.87% versus <0.01% elsewhere) and in the homozygous state causes Laron syndrome involving short stature. We find that this variant reduces height in heterozygotes by an average of 4.2 cm (-0.64 s.d.). The other variant, in the imprinted KCNQ1 gene (minor allele frequency (MAF) = 7.7% in Sardinia versus <1% elsewhere) reduces height by an average of 1.83 cm (-0.31 s.d.) when maternally inherited. Additionally, polygenic scores indicate that known height-decreasing alleles are at systematically higher frequencies in Sardinians than would be expected by genetic drift. The findings are consistent with selection for shorter stature in Sardinia and a suggestive human example of the proposed 'island effect' reducing the size of large mammals.

摘要

我们报告了基于测序的全基因组关联分析,以评估罕见变异和奠基者变异对撒丁岛6307名个体身高的影响。我们鉴定出两个具有较大效应的变异。其中一个变异在生长激素受体(GHR)基因中引入了一个终止密码子,在撒丁岛相对常见(频率为0.87%,而在其他地方<0.01%),纯合状态时会导致拉伦综合征,表现为身材矮小。我们发现该变异使杂合子身高平均降低4.2厘米(-0.64标准差)。另一个变异位于印记基因KCNQ1中(在撒丁岛的次要等位基因频率(MAF)为7.7%,而在其他地方<1%),当由母亲遗传时,身高平均降低1.83厘米(-0.31标准差)。此外,多基因评分表明,已知的降低身高的等位基因在撒丁岛的频率系统性地高于遗传漂变预期的频率。这些发现与撒丁岛对较矮身材的选择一致,并且是所提出的“岛屿效应”使大型哺乳动物体型变小的一个有启发性的人类实例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbe0/4627578/b7f1aa10ca8a/emss-64788-f0001.jpg

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