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Lipid-independent activation of a muscle-specific PKCα splicing variant.
Gao, Chen; Gong, Jianli; Cao, Nancy; Wang, Yibin; Steinberg, Susan F.
Afiliación
  • Gao C; Department of Pharmacology and System Physiology, University of Cincinnati, Cincinnati, Ohio.
  • Gong J; The Department of Pharmacology, Columbia University College of Physicians and Surgeons, New York, New York.
  • Cao N; University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
  • Wang Y; Signature Research Program in Cardiovascular and Metabolic Diseases, Duke-NUS Medical School, Singapore.
  • Steinberg SF; The Department of Pharmacology, Columbia University College of Physicians and Surgeons, New York, New York.
Am J Physiol Heart Circ Physiol ; 323(4): H825-H832, 2022 10 01.
Article en En | MEDLINE | ID: mdl-36112502
ABSTRACT
Protein kinase C-α (PKCα) plays a major role in a diverse range of cellular processes. Studies to date have defined the regulatory controls and function of PKCα entirely based upon the previously annotated ubiquitously expressed prototypical isoform. From RNA-seq-based transcriptome analysis in murine heart, we identified a previously unannotated PKCα variant produced by alternative RNA splicing. This PKCα transcript variant, which we named PKCα-novel exon (PKCα-NE), contains an extra exon between exon 16 and exon 17, and is specifically detected in adult mouse cardiac and skeletal muscle, but not other tissues; it is also detected in human hearts. This transcript variant yields a PKCα isoform with additional 16 amino acids inserted in its COOH-terminal variable region. Although the canonical PKCα enzyme is a lipid-dependent kinase, in vitro kinase assays show that PKCα-NE displays a high level of basal lipid-independent catalytic activity. Our unbiased proteomic analysis identified a specific interaction between PKCα-NE and eukaryotic elongation factor-1α (eEF1A1). Studies in cardiomyocytes link PKCα-NE expression to an increase in eEF1A1 phosphorylation and elevated protein synthesis. In summary, we have identified a previously uncharacterized muscle-specific PKCα splicing variant, PKCα-NE, with distinct biochemical properties that plays a unique role in the control of the protein synthesis machinery in cardiomyocytes.NEW & NOTEWORTHY PKCα is an important signaling molecule extensively studied in many cellular processes. However, no isoforms have been reported for PKCα except one prototypic isoform. Alternative mRNA splicing of Prkca gene was detected for the first time in rodent and human cardiac tissue, which can produce a previously unknown PKCα-novel exon (NE) isoform. The biochemistry and molecular effects of PKCα-NE are markedly different from PKCα wild type, suggesting potential functional diversity of PKCα signaling in muscle.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteómica / Proteína Quinasa C-alfa Tipo de estudio: Prognostic_studies Límite: Adult / Animals / Humans Idioma: En Revista: Am J Physiol Heart Circ Physiol Asunto de la revista: CARDIOLOGIA / FISIOLOGIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteómica / Proteína Quinasa C-alfa Tipo de estudio: Prognostic_studies Límite: Adult / Animals / Humans Idioma: En Revista: Am J Physiol Heart Circ Physiol Asunto de la revista: CARDIOLOGIA / FISIOLOGIA Año: 2022 Tipo del documento: Article