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Lamin A/C phosphorylation at serine 22 is a conserved heat shock response to regulate nuclear adaptation during stress.
Virtanen, Laura; Holm, Emilia; Halme, Mona; West, Gun; Lindholm, Fanny; Gullmets, Josef; Irjala, Juho; Heliö, Tiina; Padzik, Artur; Meinander, Annika; Eriksson, John E; Taimen, Pekka.
Afiliación
  • Virtanen L; Institute of Biomedicine and FICAN West Cancer Centre, University of Turku, 20520 Turku, Finland.
  • Holm E; Faculty of Science and Engineering, Åbo Akademi University, 20520 Turku, Finland.
  • Halme M; Institute of Biomedicine and FICAN West Cancer Centre, University of Turku, 20520 Turku, Finland.
  • West G; Institute of Biomedicine and FICAN West Cancer Centre, University of Turku, 20520 Turku, Finland.
  • Lindholm F; Institute of Biomedicine and FICAN West Cancer Centre, University of Turku, 20520 Turku, Finland.
  • Gullmets J; Institute of Biomedicine and FICAN West Cancer Centre, University of Turku, 20520 Turku, Finland.
  • Irjala J; Faculty of Science and Engineering, Åbo Akademi University, 20520 Turku, Finland.
  • Heliö T; Institute of Biomedicine and FICAN West Cancer Centre, University of Turku, 20520 Turku, Finland.
  • Padzik A; Heart and Lung Center, Helsinki University Hospital and University of Helsinki, 00029 Helsinki, Finland.
  • Meinander A; Genome Editing Core, Turku Bioscience Centre, University of Turku and Åbo Akademi University, 20520 Turku, Finland.
  • Eriksson JE; Faculty of Science and Engineering, Åbo Akademi University, 20520 Turku, Finland.
  • Taimen P; Faculty of Science and Engineering, Åbo Akademi University, 20520 Turku, Finland.
J Cell Sci ; 136(4)2023 02 15.
Article en En | MEDLINE | ID: mdl-36695453
The heat shock (HS) response is crucial for cell survival in harmful environments. Nuclear lamin A/C, encoded by the LMNA gene, contributes towards altered gene expression during HS, but the underlying mechanisms are poorly understood. Here, we show that upon HS, lamin A/C was reversibly phosphorylated at serine 22 in concert with HSF1 activation in human cells, mouse cells and Drosophila melanogaster in vivo. Consequently, the phosphorylation facilitated nucleoplasmic localization of lamin A/C and nuclear sphericity in response to HS. Interestingly, lamin A/C knock-out cells showed deformed nuclei after HS and were rescued by ectopic expression of wild-type lamin A, but not by a phosphomimetic (S22D) lamin A mutant. Furthermore, HS triggered concurrent downregulation of lamina-associated protein 2α (Lap2α, encoded by TMPO) in wild-type lamin A/C-expressing cells, but a similar response was perturbed in lamin A/C knock-out cells and in LMNA mutant patient fibroblasts, which showed impaired cell cycle arrest under HS and compromised survival at recovery. Taken together, our results suggest that the altered phosphorylation stoichiometry of lamin A/C provides an evolutionarily conserved mechanism to regulate lamina structure and serve nuclear adaptation and cell survival during HS.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Serina / Lamina Tipo A Límite: Animals / Humans Idioma: En Revista: J Cell Sci Año: 2023 Tipo del documento: Article País de afiliación: Finlandia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Serina / Lamina Tipo A Límite: Animals / Humans Idioma: En Revista: J Cell Sci Año: 2023 Tipo del documento: Article País de afiliación: Finlandia Pais de publicación: Reino Unido