| Literature DB >> 35472321 |
Peiheng Gan1, Zhaoning Wang2, Maria Gabriela Morales1, Yu Zhang1, Rhonda Bassel-Duby1, Ning Liu3, Eric N Olson4.
Abstract
Noncompaction cardiomyopathy is a common congenital cardiac disorder associated with abnormal ventricular cardiomyocyte trabeculation and impaired pump function. The genetic basis and underlying mechanisms of this disorder remain elusive. We show that the genetic deletion of RNA-binding protein with multiple splicing (Rbpms), an uncharacterized RNA-binding factor, causes perinatal lethality in mice due to congenital cardiovascular defects. The loss of Rbpms causes premature onset of cardiomyocyte binucleation and cell cycle arrest during development. Human iPSC-derived cardiomyocytes with RBPMS gene deletion have a similar blockade to cytokinesis. Sequencing analysis revealed that RBPMS plays a role in RNA splicing and influences RNAs involved in cytoskeletal signaling pathways. We found that RBPMS mediates the isoform switching of the heart-enriched LIM domain protein Pdlim5. The loss of Rbpms leads to an abnormal accumulation of Pdlim5-short isoforms, disrupting cardiomyocyte cytokinesis. Our findings connect premature cardiomyocyte binucleation to noncompaction cardiomyopathy and highlight the role of RBPMS in this process.Entities:
Keywords: Pdlim5; RNA-binding protein; Rbpms; alternative splicing; cardiomyocyte binucleation; hypertrabeculation; noncompaction cardiomyopathy; patent ductus arteriosus
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Year: 2022 PMID: 35472321 PMCID: PMC9116735 DOI: 10.1016/j.devcel.2022.03.017
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 13.417