MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndrome. (September 2014)

• Record Type: Journal Article
• Authors: Hedley, Paula L.; Carlsen, Anting L.; Christiansen, Kasper M.; Kanters, Jørgen K.; Behr, Elijah R.; Corfield, Valerie A.; Christiansen, Michael
• Is Part Of: Scandinavian journal of clinical & laboratory investigation. Volume 74:Number 6(2014)
• Page Start: 485
• Page End: 491
• Publication Date: 2014-09
• Subjects: Clinical biochemistry -- Periodicals; Physiology, Pathological -- Periodicals; Physiology, Experimental -- Periodicals; Medicine -- Research -- Periodicals; Clinical medicine -- Periodicals; 616.0072
• DOI: 10.3109/00365513.2014.905696
• Languages: English
• ISSNs: 0036-5513

Abstract

<abstract> <title>Abstract</title> <p>Long QT syndrome (LQTS) is a genetic cardiac condition associated with prolonged ventricular repolarization, primarily a result of perturbations in cardiac ion channels, which predisposes individuals to life-threatening arrhythmias. Using DNA screening and sequencing methods, over 700 different LQTS-causing mutations have been identified in 13 genes worldwide. Despite this, the genetic cause of 30–50% of LQTS is presently unknown. MicroRNAs (miRNAs) are small (∼ 22 nucleotides) noncoding RNAs which post-transcriptionally regulate gene expression by binding complementary sequences within messenger RNAs (mRNAs). The human genome encodes over 1800 miRNAs, which target about 60% of human genes. Consequently, miRNAs are likely to regulate many complex processes in the body, indeed aberrant expression of various miRNA species has been implicated in numerous disease states, including cardiovascular diseases. MiR-1 and MiR-133A are the most abundant miRNAs in the heart and have both been reported to regulate cardiac ion channels. We hypothesized that, as a consequence of their role in regulating cardiac ion channels, genetic variation in the genes which encode MiR-1 and MiR-133A might explain some cases of LQTS. Four miRNA genes (<italic>miR-1-1, miR-1-2, miR-133a-1</italic> and <italic>miR-133a-2</italic>), which encode MiR-1 and MiR-133A, were sequenced in 125 LQTS probands. No genetic variants were identified in <italic>miR-1-1</italic> or <italic>miR-133a-1</italic>; but in miR-1-2 we identified a single substitution (<italic>n.100A> G</italic>) and in <italic>miR-133a-2</italic> we identified two substitutions (<italic>n.−19G> A</italic> and <italic>n.98C> T</italic>). None of the variants affect the mature miRNA products. Our findings indicate that sequence variants of <italic>miR-1-1, miR-1-2, miR-133a-1</italic> and <italic>miR-133a-2</italic> are not a cause of LQTS in this cohort.</p> </abstract>