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人类基因变异决定24小时节律性基因表达和疾病风险。

Human genetic variation determines 24-hour rhythmic gene expression and disease risk.

作者信息

Guan Dongyin, Chen Ying, Liu Panpan, Sabo Aniko

机构信息

Baylor College of Medicine.

出版信息

Res Sq. 2024 Aug 5:rs.3.rs-4790200. doi: 10.21203/rs.3.rs-4790200/v1.

DOI:10.21203/rs.3.rs-4790200/v1
PMID:39149455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11326361/
Abstract

24-hour biological rhythms are essential to maintain physiological homeostasis. Disruption of these rhythms increases the risks of multiple diseases. The biological rhythms are known to have a genetic basis formed by core clock genes, but how individual genetic variation shapes the oscillating transcriptome and contributes to human chronophysiology and disease risk is largely unknown. Here, we mapped interactions between temporal gene expression and genotype to identify quantitative trait loci (QTLs) contributing to rhythmic gene expression. These newly identified QTLs were termed as rhythmic QTLs (rhyQTLs), which determine previously unappreciated rhythmic genes in human subpopulations with specific genotypes. Functionally, rhyQTLs and their associated rhythmic genes contribute extensively to essential chronophysiological processes, including bile acid and lipid metabolism. The identification of rhyQTLs sheds light on the genetic mechanisms of gene rhythmicity, offers mechanistic insights into variations in human disease risk, and enables precision chronotherapeutic approaches for patients.

摘要

24小时生物节律对于维持生理稳态至关重要。这些节律的紊乱会增加多种疾病的风险。已知生物节律具有由核心时钟基因形成的遗传基础,但个体遗传变异如何塑造振荡转录组并影响人类时间生理学和疾病风险在很大程度上尚不清楚。在这里,我们绘制了时间基因表达与基因型之间的相互作用,以确定有助于节律性基因表达的数量性状位点(QTL)。这些新发现的QTL被称为节律性QTL(rhyQTL),它们在具有特定基因型的人类亚群中决定了以前未被认识的节律性基因。在功能上,rhyQTL及其相关的节律性基因广泛参与基本的时间生理过程,包括胆汁酸和脂质代谢。rhyQTL的鉴定揭示了基因节律性的遗传机制,为人类疾病风险的变异提供了机制性见解,并为患者提供了精准的时间治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11326361/e590e00575fb/nihpp-rs4790200v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11326361/4c9b76f4dfc0/nihpp-rs4790200v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11326361/31fdce8def85/nihpp-rs4790200v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11326361/80a65274c2df/nihpp-rs4790200v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11326361/e590e00575fb/nihpp-rs4790200v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11326361/4c9b76f4dfc0/nihpp-rs4790200v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11326361/31fdce8def85/nihpp-rs4790200v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11326361/80a65274c2df/nihpp-rs4790200v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11326361/e590e00575fb/nihpp-rs4790200v1-f0004.jpg

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本文引用的文献

1
Embracing cancer complexity: Hallmarks of systemic disease.拥抱癌症的复杂性:全身性疾病的特征。
Cell. 2024 Mar 28;187(7):1589-1616. doi: 10.1016/j.cell.2024.02.009.
2
Exome sequencing identifies genes associated with sleep-related traits.外显子组测序鉴定与睡眠相关特征相关的基因。
Nat Hum Behav. 2024 Mar;8(3):576-589. doi: 10.1038/s41562-023-01785-5. Epub 2024 Jan 4.
3
IGF2 deficiency promotes liver aging through mitochondrial dysfunction and upregulated CEBPB signaling in D-galactose-induced aging mice.IGF2 缺乏通过线粒体功能障碍和 D-半乳糖诱导衰老小鼠中 CEBPB 信号的上调促进肝脏衰老。
Mol Med. 2023 Nov 28;29(1):161. doi: 10.1186/s10020-023-00752-0.
4
Reducing nighttime light exposure in the urban environment to benefit human health and society.减少城市环境中的夜间光照暴露,以造福人类健康和社会。
Science. 2023 Jun 16;380(6650):1130-1135. doi: 10.1126/science.adg5277. Epub 2023 Jun 15.
5
The EN-TEx resource of multi-tissue personal epigenomes & variant-impact models.多组织个人表观基因组和变异影响模型的 EN-TEx 资源。
Cell. 2023 Mar 30;186(7):1493-1511.e40. doi: 10.1016/j.cell.2023.02.018.
6
Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids.代谢组学研究重度抑郁症发现多不饱和脂肪酸的潜在因果关联。
Biol Psychiatry. 2023 Oct 15;94(8):630-639. doi: 10.1016/j.biopsych.2023.01.027. Epub 2023 Feb 9.
7
Sex-dimorphic and age-dependent organization of 24-hour gene expression rhythms in humans.人类24小时基因表达节律的性别二态性及年龄依赖性组织
Science. 2023 Feb 3;379(6631):478-483. doi: 10.1126/science.add0846. Epub 2023 Feb 2.
8
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource.NHGRI-EBI GWAS 目录:知识库和存储资源。
Nucleic Acids Res. 2023 Jan 6;51(D1):D977-D985. doi: 10.1093/nar/gkac1010.
9
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Nat Cell Biol. 2022 Oct;24(10):1516-1527. doi: 10.1038/s41556-022-00992-y. Epub 2022 Oct 6.
10
Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation.通过药物靶点孟德尔随机化来描述脂质调节治疗的代谢组学特征。
PLoS Biol. 2022 Feb 25;20(2):e3001547. doi: 10.1371/journal.pbio.3001547. eCollection 2022 Feb.