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基于转录组全基因组关联研究优先考虑男性型秃发的易感性基因。

Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study.

机构信息

Department of Life Sciences, Dongguk University, Seoul, 04620, Republic of Korea.

出版信息

Hum Genomics. 2024 Apr 2;18(1):34. doi: 10.1186/s40246-024-00591-y.

DOI:10.1186/s40246-024-00591-y
PMID:38566255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10985920/
Abstract

BACKGROUND

Male-pattern baldness (MPB) is the most common cause of hair loss in men. It can be categorized into three types: type 2 (T2), type 3 (T3), and type 4 (T4), with type 1 (T1) being considered normal. Although various MPB-associated genetic variants have been suggested, a comprehensive study for linking these variants to gene expression regulation has not been performed to the best of our knowledge.

RESULTS

In this study, we prioritized MPB-related tissue panels using tissue-specific enrichment analysis and utilized single-tissue panels from genotype-tissue expression version 8, as well as cross-tissue panels from context-specific genetics. Through a transcriptome-wide association study and colocalization analysis, we identified 52, 75, and 144 MPB associations for T2, T3, and T4, respectively. To assess the causality of MPB genes, we performed a conditional and joint analysis, which revealed 10, 11, and 54 putative causality genes for T2, T3, and T4, respectively. Finally, we conducted drug repositioning and identified potential drug candidates that are connected to MPB-associated genes.

CONCLUSIONS

Overall, through an integrative analysis of gene expression and genotype data, we have identified robust MPB susceptibility genes that may help uncover the underlying molecular mechanisms and the novel drug candidates that may alleviate MPB.

摘要

背景

男性型脱发(MPB)是男性脱发最常见的原因。它可以分为三种类型:2 型(T2)、3 型(T3)和 4 型(T4),1 型(T1)被认为是正常的。尽管已经提出了各种与 MPB 相关的遗传变异,但据我们所知,尚未进行将这些变异与基因表达调控联系起来的综合研究。

结果

在这项研究中,我们使用组织特异性富集分析来确定与 MPB 相关的组织面板,并利用基因型组织表达版本 8 的单一组织面板以及特定于上下文的遗传交叉组织面板。通过全转录组关联研究和共定位分析,我们分别鉴定出 T2、T3 和 T4 的 52、75 和 144 个 MPB 关联。为了评估 MPB 基因的因果关系,我们进行了条件和联合分析,分别揭示了 T2、T3 和 T4 的 10、11 和 54 个假定因果基因。最后,我们进行了药物重定位,并确定了与 MPB 相关基因相关的潜在药物候选物。

结论

总的来说,通过基因表达和基因型数据的综合分析,我们已经确定了稳健的 MPB 易感基因,这可能有助于揭示潜在的分子机制和可能缓解 MPB 的新型药物候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/1c882a105cbd/40246_2024_591_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/fbf5093b5dec/40246_2024_591_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/26ebe2bd8ccb/40246_2024_591_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/83964380474f/40246_2024_591_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/8cfca825e1c4/40246_2024_591_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/3cf55e1a77dd/40246_2024_591_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/1c882a105cbd/40246_2024_591_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/fbf5093b5dec/40246_2024_591_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/26ebe2bd8ccb/40246_2024_591_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/83964380474f/40246_2024_591_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/8cfca825e1c4/40246_2024_591_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/3cf55e1a77dd/40246_2024_591_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918c/10985920/1c882a105cbd/40246_2024_591_Fig6_HTML.jpg

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Role of Smoking in Androgenetic Alopecia: A Systematic Review.吸烟在雄激素性脱发中的作用:一项系统综述。
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