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Genetics meets epigenetics: Genetic variants that modulate noncoding RNA in cardiovascular diseases

机译:遗传学符合EPigenetics:遗传变异,调节心血管疾病中的非沉积RNA

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摘要

After the recent description of the human genome by the ENCODE and the FANTOM consortia, major attention has been addressed to the so-called "genomic noise", which mainly consists of noncoding RNAs (ncRNAs). Among them, microRNAs and long non-coding RNAs have been demonstrated to modulate gene expression and to be involved in several human diseases. Since ncRNAs and their targets are encoded in the genome, genetic principles apply. Common variants are supposed to influence the expression level and the functionality of ncRNAs, with subsequent differential regulation of their target genes. Moreover, several reports showed that polymorphisms in ncRNA or their target genes play a role in the development of cardiovascular adverse phenotype. Here, we provide an overview of the effects of these variations in cardiovascular diseases. (c) 2015 Elsevier Ltd. All rights reserved.
机译:在通过编码和芬特联盟的人类基因组的最近描述后,主要关注所谓的“基因组噪声”,主要由非编码的RNA(NCRNA)组成。 其中,已经证明了MicroRNA和长期非编码RNA调节基因表达并参与几种人类疾病。 由于NCRNA及其靶标在基因组中编码,遗传原理适用。 应该影响NCRNA的表达水平和NCRNA的功能性,随后对其靶基因进行差异调节。 此外,若干报道显示NCRNA或其靶基因中的多态性在心血管不良表型的发育中发挥作用。 在这里,我们概述了这些变化在心血管疾病中的影响。 (c)2015 Elsevier Ltd.保留所有权利。

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