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人类毛发相关表型的遗传学中重叠的关联信号及其对预测性 DNA 分析的相关性。

Overlapping association signals in the genetics of hair-related phenotypes in humans and their relevance to predictive DNA analysis.

机构信息

Malopolska Centre of Biotechnology, Jagiellonian University, Kraków, Poland.

Faculty of Mathematics and Computer Science, Nicolaus Copernicus University in Toruń, Toruń, Poland.

出版信息

Forensic Sci Int Genet. 2022 Jul;59:102693. doi: 10.1016/j.fsigen.2022.102693. Epub 2022 Mar 25.

DOI:10.1016/j.fsigen.2022.102693
PMID:35398773
Abstract

Genetic prediction of different hair phenotypes can help reconstruct the physical appearance of an individual whose biological sample is analyzed in criminal and identification cases. Up to date, forensic prediction models for hair colour, hair shape, hair loss and hair greying have been developed, but studies investigating predictability of hair thickness and density traits are missing. First data suggesting overlapping associations in various hair features have emerged in recent years, suggesting partially common genetic basis and molecular mechanisms, and this knowledge can be used for predictive purposes. Here we aim to broaden our understanding of the genetics underlying head, facial and body hair thickness and density traits and examine the association for a set of literature SNPs. We characterize the overlap in SNP association for various hair phenotypes, the extent of genetic interactions and the potential for genetic prediction. The study involved 999 samples from Poland, genotyped for 240 SNPs with targeted next-generation sequencing. Logistic regression methods were applied for association and prediction analyses while entropy-based approach was used for interaction testing. As a result, we refined known associations for monobrow and hairiness (PAX3, 5q13.2, TBX) and identified two novel association signals in IGFBP5 and VDR. Both genes were among top significant loci, showed broad association with different hair-related traits and were implicated in multiple interaction effects. Overall, for 14.7% of SNPs previously associated with head hair loss and/or hair shape, a positive signal of association was revealed with at least one hair feature studied in the current research. Overlap in association with at least two hair-related traits was demonstrated for 24 distinct loci. We showed that the associated SNPs explain ∼5-30% of the variation observed in particular hair traits and allow moderate accuracy of prediction. The highest accuracy was achieved for hairiness level prediction in females (AUC = 0.69 for the "none", 0.69 for the "low" and 0.76 for the "excessive" hairiness category) and monobrow (AUC = 0.69 for the "none", 0.62 for the "slight" and 0.70 for the "significant" monobrow category) with 33% of the variation in hairiness level in females explained by 7 SNPs and age, and 20% of the variation in monobrow captured by 7 SNPs and sex. Our study presents clear evidence of pleiotropy and epistasis in the genetics of hair traits. The acquired knowledge may have practical application in forensics, as well as in the cosmetic industry and anthropological research.

摘要

不同毛发表型的遗传预测有助于重建分析犯罪和识别案件中生物样本的个体的外貌。迄今为止,已经开发出用于预测头发颜色、头发形状、脱发和头发变白的法医预测模型,但研究调查头发厚度和密度特征的可预测性的研究尚属空白。近年来,各种毛发特征的重叠关联数据已经出现,这表明存在部分共同的遗传基础和分子机制,这些知识可用于预测目的。在这里,我们旨在更深入地了解头部、面部和身体毛发厚度和密度特征的遗传基础,并研究一组文献 SNP 的关联。我们描述了各种毛发表型的 SNP 关联的重叠程度、遗传相互作用的程度以及遗传预测的潜力。该研究涉及来自波兰的 999 个样本,通过靶向下一代测序对 240 个 SNP 进行了基因分型。应用逻辑回归方法进行关联和预测分析,同时应用基于熵的方法进行相互作用测试。结果,我们细化了单眉和多毛(PAX3、5q13.2、TBX)的已知关联,并在 IGFBP5 和 VDR 中确定了两个新的关联信号。这两个基因都位于最重要的基因座之一,与不同的毛发相关特征广泛关联,并涉及多个相互作用效应。总的来说,对于以前与头部脱发和/或头发形状相关的 14.7%的 SNP,与当前研究中研究的至少一种毛发特征相关的阳性关联信号被揭示出来。与至少两种毛发相关特征的重叠关联在 24 个不同的基因座中得到证实。我们表明,相关 SNP 解释了特定毛发特征观察到的变异的 5-30%,并允许进行中等准确性的预测。在女性多毛程度的预测中达到了最高的准确性(无毛的 AUC=0.69,低毛的 AUC=0.69,多毛的 AUC=0.76),以及单眉的预测(无眉的 AUC=0.69,轻度的 AUC=0.62,显著的 AUC=0.70),7 个 SNP 解释了女性多毛程度的 33%的变异,以及 7 个 SNP 和性别解释了单眉的 20%的变异。我们的研究提供了毛发特征遗传中明显的多效性和上位性证据。获得的知识在法医学、化妆品行业和人类学研究中可能具有实际应用。

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