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Oxygen-dependent proteolysis regulates the stability of angiosperm polycomb repressive complex 2 subunit VERNALIZATION 2.
Gibbs, Daniel J; Tedds, Hannah M; Labandera, Anne-Marie; Bailey, Mark; White, Mark D; Hartman, Sjon; Sprigg, Colleen; Mogg, Sophie L; Osborne, Rory; Dambire, Charlene; Boeckx, Tinne; Paling, Zachary; Voesenek, Laurentius A C J; Flashman, Emily; Holdsworth, Michael J.
Afiliación
  • Gibbs DJ; School of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK. d.gibbs@bham.ac.uk.
  • Tedds HM; School of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK.
  • Labandera AM; School of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK.
  • Bailey M; School of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK.
  • White MD; Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK.
  • Hartman S; Plant Ecophysiology, Institute of Environmental Biology, Faculty of Science, Utrecht University, Padualaan 8, Utrecht, 3584 CH, The Netherlands.
  • Sprigg C; School of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK.
  • Mogg SL; School of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK.
  • Osborne R; School of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK.
  • Dambire C; School of Biosciences, University of Nottingham, Loughborough, LE12 5RD, UK.
  • Boeckx T; School of Biosciences, University of Nottingham, Loughborough, LE12 5RD, UK.
  • Paling Z; School of Biosciences, University of Birmingham, Edgbaston, B15 2TT, UK.
  • Voesenek LACJ; Plant Ecophysiology, Institute of Environmental Biology, Faculty of Science, Utrecht University, Padualaan 8, Utrecht, 3584 CH, The Netherlands.
  • Flashman E; Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK.
  • Holdsworth MJ; School of Biosciences, University of Nottingham, Loughborough, LE12 5RD, UK. michael.holdsworth@nottingham.ac.uk.
Nat Commun ; 9(1): 5438, 2018 12 21.
Article en En | MEDLINE | ID: mdl-30575749
The polycomb repressive complex 2 (PRC2) regulates epigenetic gene repression in eukaryotes. Mechanisms controlling its developmental specificity and signal-responsiveness are poorly understood. Here, we identify an oxygen-sensitive N-terminal (N-) degron in the plant PRC2 subunit VERNALIZATION(VRN) 2, a homolog of animal Su(z)12, that promotes its degradation via the N-end rule pathway. We provide evidence that this N-degron arose early during angiosperm evolution via gene duplication and N-terminal truncation, facilitating expansion of PRC2 function in flowering plants. We show that proteolysis via the N-end rule pathway prevents ectopic VRN2 accumulation, and that hypoxia and long-term cold exposure lead to increased VRN2 abundance, which we propose may be due to inhibition of VRN2 turnover via its N-degron. Furthermore, we identify an overlap in the transcriptional responses to hypoxia and prolonged cold, and show that VRN2 promotes tolerance to hypoxia. Our work reveals a mechanism for post-translational regulation of VRN2 stability that could potentially link environmental inputs to the epigenetic control of plant development.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Nucleares / Proteínas Portadoras / Regulación de la Expresión Génica de las Plantas / Evolución Molecular / Proteínas de Arabidopsis / Complejo Represivo Polycomb 2 Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Nucleares / Proteínas Portadoras / Regulación de la Expresión Génica de las Plantas / Evolución Molecular / Proteínas de Arabidopsis / Complejo Represivo Polycomb 2 Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2018 Tipo del documento: Article