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Obesity Associated Modulation of miRNA and Co-Regulated Target Transcripts in Human Adipose Tissue of Non-Diabetic Subjects

机译:肥胖相关的非糖尿病对象的人类脂肪组织中的miRNA和共同调控的目标转录物的调控。

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摘要

Objective: Micro RNAs (miRNAs) are a class of non-coding regulatory RNAs. We performed a transcriptome-wide analysis of subcutaneous adipose tissue and in vitro studies to identify miRNAs and co-regulated target transcripts associated with insulin sensitivity (SI) and obesity in human. Methods: We selected 20 insulin-resistant (IR, SI=2.0±0.7) and 20 insulin-sensitive (IS, SI=7.2±2.3) subjects from a cohort of 117 metabolically characterized non-diabetic Caucasians for comparison. Results: After global profiling, 3 miRNAs had marginally different expressions between IR and IS subjects. A total of 14 miRNAs were significantly correlated with %fat mass, body mass index (BMI), or SI. The qRT-PCR validated the correlation of miR-148a-3p with BMI (r=-0.70, P=2.73X10-6). MiRNA target filtering analysis identified DNA methyltransferase 1 (DNMT1) as one of the target genes of miR-148a-3p. DNMT1 expression in adipose tissue was positively correlated with BMI (r=0.47, p=8.42X10-7) and was inversely correlated with miR-148a-3p (r=-0.34). Differentiation of SGBS preadipocytes showed up-regulation of miR-148a-3p and down-regulation of DNMT1 in differentiated adipocytes. After transfecting miR-148a-3p mimics into HeLa-S3 cells, DNMT1 was down-regulated, while transfection of adipose stem cells with miR-148a-3p inhibitor up-regulated DNMT1. Conclusions: Our results indicate that miR-148a-3p-mediated regulation of DNMT1 expression may play a mechanistic role in obesity.
机译:目的:微小RNA(miRNA)是一类非编码调控RNA。我们对皮下脂肪组织进行了转录组范围的分析,并进行了体外研究,以鉴定与人类胰岛素敏感性(SI)和肥胖症相关的miRNA和共同调控的目标转录本。方法:我们从117名具有代谢特征的非糖尿病高加索人队列中选择了20名胰岛素抵抗(IR,SI = 2.0±0.7)和20名胰岛素敏感(IS,SI = 7.2±2.3)受试者进行比较。结果:整体分析后,IR和IS受试者之间3个miRNA的表达略有不同。共有14个miRNA与%脂肪质量,体重指数(BMI)或SI显着相关。 qRT-PCR验证了miR-148a-3p与BMI的相关性(r = -0.70,P = 2.73X10 -6 )。 MiRNA靶标过滤分析确定DNA甲基转移酶1(DNMT1)为miR-148a-3p的靶标基因之一。脂肪组织中DNMT1的表达与BMI呈正相关(r = 0.47,p = 8.42X10 -7 ),与miR-148a-3p呈负相关(r = -0.34)。 SGBS前脂肪细胞的分化显示miR-148a-3p的上调和mR-148a-3p的下调DNMT1在分化的脂肪细胞中。转染miR-148a-3p模拟物后进入HeLa-S3细胞后,DNMT1被下调,而转染含miR-148a-3p抑制剂的脂肪干细胞上调DNMT1。结论:我们的结果表明,miR-148a-3p介导的调节DNMT1表达的改变可能在肥胖中起机械作用。

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