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Rtf1 Transcriptionally Regulates Neonatal and Adult Cardiomyocyte Biology.
Langenbacher, Adam D; Lu, Fei; Crisman, Lauren; Huang, Zi Yi Stephanie; Chapski, Douglas J; Vondriska, Thomas M; Wang, Yibin; Gao, Chen; Chen, Jau-Nian.
Afiliación
  • Langenbacher AD; Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, CA 90025, USA.
  • Lu F; Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, CA 90025, USA.
  • Crisman L; Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, CA 90025, USA.
  • Huang ZYS; Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, CA 90025, USA.
  • Chapski DJ; Departments of Anesthesiology, Medicine, and Physiology, David Geffen School of Medicine, University of California, Los Angeles, CA 90025, USA.
  • Vondriska TM; Departments of Anesthesiology, Medicine, and Physiology, David Geffen School of Medicine, University of California, Los Angeles, CA 90025, USA.
  • Wang Y; Departments of Anesthesiology, Medicine, and Physiology, David Geffen School of Medicine, University of California, Los Angeles, CA 90025, USA.
  • Gao C; Signature Research Program in Cardiovascular and Metabolic Diseases, Duke-NUS School of Medicine and National Heart Center of Singapore, Singapore 169857, Singapore.
  • Chen JN; Departments of Anesthesiology, Medicine, and Physiology, David Geffen School of Medicine, University of California, Los Angeles, CA 90025, USA.
J Cardiovasc Dev Dis ; 10(5)2023 May 20.
Article en En | MEDLINE | ID: mdl-37233188
The PAF1 complex component Rtf1 is an RNA Polymerase II-interacting transcription regulatory protein that promotes transcription elongation and the co-transcriptional monoubiquitination of histone 2B. Rtf1 plays an essential role in the specification of cardiac progenitors from the lateral plate mesoderm during early embryogenesis, but its requirement in mature cardiac cells is unknown. Here, we investigate the importance of Rtf1 in neonatal and adult cardiomyocytes using knockdown and knockout approaches. We demonstrate that loss of Rtf1 activity in neonatal cardiomyocytes disrupts cell morphology and results in a breakdown of sarcomeres. Similarly, Rtf1 ablation in mature cardiomyocytes of the adult mouse heart leads to myofibril disorganization, disrupted cell-cell junctions, fibrosis, and systolic dysfunction. Rtf1 knockout hearts eventually fail and exhibit structural and gene expression defects resembling dilated cardiomyopathy. Intriguingly, we observed that loss of Rtf1 activity causes a rapid change in the expression of key cardiac structural and functional genes in both neonatal and adult cardiomyocytes, suggesting that Rtf1 is continuously required to support expression of the cardiac gene program.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Cardiovasc Dev Dis Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Cardiovasc Dev Dis Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
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