Long Noncoding RNA TRIBAL Links the 8q24.13 Locus to Hepatic Lipid Metabolism and Coronary Artery Disease.

IF 6 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Sébastien Soubeyrand, Paulina Lau, Majid Nikpay, Lijiang Ma, Johan L M Bjorkegren, Ruth McPherson
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引用次数: 0

Abstract

Background: Genome-wide association studies identified a 20-Kb region of chromosome 8 (8q24.13) associated with plasma lipids, hepatic steatosis, and risk for coronary artery disease. The region is proximal to TRIB1, and given its well-established role in lipid regulation in animal models, TRIB1 has been proposed to mediate the contribution of the 8q24.13 locus to these traits. This region overlaps a gene encoding the primate-specific long noncoding RNA transcript TRIBAL/TRIB1AL (TRIB1-associated locus), but the contribution of TRIBAL to coronary artery disease risk remains untested.

Methods: Using recently available expression quantitative trait loci data and hepatocyte models, we further investigated this locus by Mendelian randomization analysis. Following antisense oligonucleotide targeting of TRIBAL, transcription array, quantitative reverse transcription polymerase chain reaction, and enrichment analyses were performed and effects on apoB and triglyceride secretion were determined.

Results: Mendelian randomization analysis supports a causal relationship between genetically determined hepatic TRIBAL expression and markers of hepatic steatosis and coronary artery disease risk. By contrast, expression data sets did not support expression quantitative trait loci relationships between coronary artery disease-associated variants and TRIB1. TRIBAL suppression reduced the expression of key regulators of triglyceride metabolism and bile acid synthesis. Enrichment analyses identified patterns consistent with impaired metabolic functions, including reduced triglyceride and cholesterol handling ability. Furthermore, TRIBAL suppression was associated with reduced hepatocyte secretion of triglycerides.

Conclusions: This work identifies TRIBAL as a gene bridging the genotype-phenotype relationship at the 8q24.13 locus with effects on genes regulating hepatocyte lipid metabolism and triglyceride secretion.

长链非编码RNA tribe将8q24.13位点与肝脂质代谢和冠状动脉疾病联系起来。
背景:全基因组关联研究发现,8号染色体(8q24.13)上一个20 kb的区域与血脂、肝脂肪变性和冠状动脉疾病的风险相关。该区域靠近TRIB1,鉴于其在动物模型中脂质调节中的作用,已经提出TRIB1介导8q24.13位点对这些性状的贡献。该区域与一个编码灵长类特异性长非编码RNA转录本tribe /TRIB1AL (trib1相关位点)的基因重叠,但tribe对冠状动脉疾病风险的贡献尚未得到验证。方法:利用最近获得的表达数量性状位点数据和肝细胞模型,采用孟德尔随机化分析方法对该位点进行进一步研究。在对TRIBAL进行反义寡核苷酸靶向后,进行转录阵列、qRT-PCR和富集分析,并确定对载脂蛋白ob和甘油三酯分泌的影响。结果:孟德尔随机化分析支持遗传决定的肝脏tribe表达与肝脂肪变性和冠状动脉疾病风险标志物之间的因果关系。相比之下,表达数据集不支持冠状动脉疾病相关变异与TRIB1之间的表达数量性状位点关系。部落抑制降低了甘油三酯代谢和胆汁酸合成的关键调节因子的表达。富集分析确定了与代谢功能受损相一致的模式,包括甘油三酯和胆固醇处理能力降低。此外,部落抑制与肝细胞甘油三酯分泌减少有关。结论:本研究确定了TRIBAL基因在8q24.13位点连接了基因型-表型关系,并影响了调节肝细胞脂质代谢和甘油三酯分泌的基因。
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来源期刊
Circulation: Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
9.20
自引率
5.40%
发文量
144
期刊介绍: Circulation: Genomic and Precision Medicine is a distinguished journal dedicated to advancing the frontiers of cardiovascular genomics and precision medicine. It publishes a diverse array of original research articles that delve into the genetic and molecular underpinnings of cardiovascular diseases. The journal's scope is broad, encompassing studies from human subjects to laboratory models, and from in vitro experiments to computational simulations. Circulation: Genomic and Precision Medicine is committed to publishing studies that have direct relevance to human cardiovascular biology and disease, with the ultimate goal of improving patient care and outcomes. The journal serves as a platform for researchers to share their groundbreaking work, fostering collaboration and innovation in the field of cardiovascular genomics and precision medicine.
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