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Dnmt2/Trdmt1 As Mediator of Rna Polymerase Ii Transcriptional Activity in Cardiac Growth Publisher Pubmed



Ghanbarian H1 ; Wagner N2, 3 ; Polo B3 ; Baudouy D2, 3 ; Kiani J5 ; Michiels JF2, 4 ; Cuzin F3 ; Rassoulzadegan M3 ; Wagner KD2, 3
Authors
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Authors Affiliations
  1. 1. Biotechnology Department, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  2. 2. Institute for Research on Cancer and Aging, Nice (IRCAN), University of Nice Sophia-Antipolis, CNRS UMR7284/INSERM U1081, Faculty of Medicine, Nice, France
  3. 3. Univ. Nice Sophia Antipolis, CNRS, Inserm, IBV, Nice, 06100, France
  4. 4. Department of Pathology, CHU Nice, Nice, France
  5. 5. Department of Molecular Medicine, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran

Source: PLoS ONE Published:2016


Abstract

Dnmt2/Trdmt1 is a methyltransferase, which has been shown to methylate tRNAs. Deficient mutants were reported to exhibit various, seemingly unrelated, defects in development and RNA-mediated epigenetic heredity. Here we report a role in a distinct developmental regulation effected by a noncoding RNA. We show that Dnmt2-deficiency in mice results in cardiac hypertrophy. Echocardiographic measurements revealed that cardiac function is preserved notwithstanding the increased dimensions of the organ due to cardiomyocyte enlargement. Mechanistically, activation of the P-TEFb complex, a critical step for cardiac growth, results from increased dissociation of the negatively regulating Rn7sk non-coding RNA component in Dnmt2-deficient cells. Our data suggest that Dnmt2 plays an unexpected role for regulation of cardiac growth by modulating activity of the P-TEFb complex. © 2016 Ghanbarian et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.