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Review
. 2014 Feb;126(3):183-94.
doi: 10.1042/CS20130203.

MicroRNAs in the onset and development of cardiovascular disease

Affiliations
Review

MicroRNAs in the onset and development of cardiovascular disease

Kasey C Vickers et al. Clin Sci (Lond). 2014 Feb.

Abstract

Physiological and pathological roles for small non-encoding miRNAs (microRNAs) in the cardiovascular system have recently emerged and are now widely studied. The discovery of widespread functions of miRNAs has increased the complexity of gene-regulatory processes and networks in both the cardiovascular system and cardiovascular diseases. Indeed, it has recently been shown that miRNAs are implicated in the regulation of many of the steps leading to the development of cardiovascular disease. These findings represent novel aspects in miRNA biology and, therefore, our understanding of the role of these miRNAs during the pathogenesis of cardiovascular disease is critical for the development of novel therapies and diagnostic interventions. The present review will focus on understanding how miRNAs are involved in the onset and development of cardiovascular diseases.

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Figures

Figure 1
Figure 1. Schematic representation of miRNA biogenesis
miRNA biogenesis is initiated with the processing of primary miRNA transcripts in the nucleus by DROSHA/DGCR8, to generate a pre-miRNA. Pre-miRNA is exported to the cytoplasm by Exportin 5 and further processed into a miRNA duplex by Dicer. One of the single stands (mature miRNA) is incorporated into RISC and binds the 3′-UTR of the target miRNA leading to mRNA degradation or translational repression. RNA pol II, RNA polymerase II.

References

    1. Bartel DP. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell. 2004;116:281–297. - PubMed
    1. Sonkoly E, Stahle M, Pivarcsi A. MicroRNAs and immunity: novel players in the regulation of normal immune function and inflammation. Semin Cancer Biol. 2008;18:131–140. - PubMed
    1. Grimson A, Farh KK, Johnston WK, Garrett-Engele P, Lim LP, Bartel DP. MicroRNA targeting specificity in mammals: determinants beyond seed pairing. Mol Cell. 2007;27:91–105. - PMC - PubMed
    1. Lim LP, Lau NC, Garrett-Engele P, Grimson A, Schelter JM, Castle J, Bartel DP, Linsley PS, Johnson JM. Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs. Nature. 2005;433:769–773. - PubMed
    1. Lee RC, Feinbaum RL, Ambros V. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell. 1993;75:843–854. - PubMed

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