脂肪组织的变异-功能方法:对心脏代谢紊乱的见解。

IF 11.1 Q1 CELL BIOLOGY
Sophia Metz, Jonathan Robert Belanich, Melina Claussnitzer, Tuomas Oskari Kilpeläinen
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引用次数: 0

摘要

全基因组关联研究(GWASs)已经确定了数千个与心脏代谢疾病相关的遗传位点。然而,这些基因座的功能解释仍然是一个艰巨的挑战。对于脂肪组织来说尤其如此,脂肪组织是全身代谢和各种心脏代谢疾病发病机制的关键器官。我们讨论了如何使用变异到功能(V2F)方法来阐明GWAS基因座通过直接影响脂肪组织而增加心脏代谢紊乱风险的机制。我们概述了最有可能携带脂肪相关变异的GWAS性状,并总结了确定相关位点的假定因果变异、基因和细胞类型的工具。我们解释了如何大规模扰动实验,结合成像和多组学,可以用来筛选变异对细胞表型的影响,以及这些表型如何与生理机制联系在一起。最后,我们讨论了V2F研究面临的挑战和机遇,并提出了未来研究的路线图。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Variant-to-function approaches for adipose tissue: Insights into cardiometabolic disorders.

Genome-wide association studies (GWASs) have identified thousands of genetic loci associated with cardiometabolic disorders. However, the functional interpretation of these loci remains a daunting challenge. This is particularly true for adipose tissue, a critical organ in systemic metabolism and the pathogenesis of various cardiometabolic diseases. We discuss how variant-to-function (V2F) approaches are used to elucidate the mechanisms by which GWAS loci increase the risk of cardiometabolic disorders by directly influencing adipose tissue. We outline GWAS traits most likely to harbor adipose-related variants and summarize tools to pinpoint the putative causal variants, genes, and cell types for the associated loci. We explain how large-scale perturbation experiments, coupled with imaging and multi-omics, can be used to screen variants' effects on cellular phenotypes and how these phenotypes can be tied to physiological mechanisms. Lastly, we discuss the challenges and opportunities that lie ahead for V2F research and propose a roadmap for future studies.

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CiteScore
7.10
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