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人类基因连接组预测的新型棕色脂肪组织候选基因。

Novel brown adipose tissue candidate genes predicted by the human gene connectome.

机构信息

PROFITH 'PROmoting FITness and Health Through Physical Activity' Research Group, Sport and Health University Research Institute (iMUDS), University of Granada, Granada, Spain.

Department of Ecology and Evolutionary Biology, University of Arizona, Tucson, AZ, USA.

出版信息

Sci Rep. 2022 May 9;12(1):7614. doi: 10.1038/s41598-022-11317-2.

Abstract

Brown adipose tissue (BAT) is a promising therapeutic target against obesity. Therefore, research on the genetic architecture of BAT could be key for the development of successful therapies against this complex phenotype. Hypothesis-driven candidate gene association studies are useful for studying genetic determinants of complex traits, but they are dependent upon the previous knowledge to select candidate genes. Here, we predicted 107 novel-BAT candidate genes in silico using the uncoupling protein one (UCP1) as the hallmark of BAT activity. We first identified the top 1% of human genes predicted by the human gene connectome to be biologically closest to the UCP1, estimating 167 additional pathway genes (BAT connectome). We validated this prediction by showing that 60 genes already associated with BAT were included in the connectome and they were biologically closer to each other than expected by chance (p < 2.2 × 10). The rest of genes (107) are potential candidates for BAT, being also closer to known BAT genes and more expressed in BAT biopsies than expected by chance (p < 2.2 × 10; p = 4.39 × 10). The resulting new list of predicted human BAT genes should be useful for the discovery of novel BAT genes and metabolic pathways.

摘要

棕色脂肪组织 (BAT) 是治疗肥胖症的有前途的治疗靶点。因此,对 BAT 的遗传结构的研究可能是开发针对这种复杂表型的成功疗法的关键。基于假设的候选基因关联研究对于研究复杂性状的遗传决定因素很有用,但它们依赖于先前的知识来选择候选基因。在这里,我们使用解偶联蛋白 1 (UCP1) 作为 BAT 活性的标志,通过计算在计算机上预测了 107 个新的 BAT 候选基因。我们首先确定了人类基因连接组中预测的最接近 UCP1 的前 1%的人类基因,估计了另外 167 个途径基因(BAT 连接组)。我们通过证明已经与 BAT 相关的 60 个基因包含在连接组中,并且它们彼此之间的生物学关系比随机预期更密切(p < 2.2 × 10)来验证了这一预测。其余的基因(107 个)是 BAT 的潜在候选基因,它们与已知的 BAT 基因也更接近,并且在 BAT 活检中的表达比随机预期更密切(p < 2.2 × 10;p = 4.39 × 10)。由此产生的新的人类 BAT 基因预测列表应该有助于发现新的 BAT 基因和代谢途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ee/9085833/84e65d8c7a1a/41598_2022_11317_Fig1_HTML.jpg

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