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Glutathione accelerates the cell cycle and cellular reprogramming in plant regeneration.
Lee, Laura R; Guillotin, Bruno; Rahni, Ramin; Hutchison, Chanel; Desvoyes, Bénédicte; Gutierrez, Crisanto; Birnbaum, Kenneth D.
Afiliação
  • Lee LR; New York University, Center for Genomics and Systems Biology, Department of Biology, NY, New York, 10003, USA.
  • Guillotin B; New York University, Center for Genomics and Systems Biology, Department of Biology, NY, New York, 10003, USA.
  • Rahni R; New York University, Center for Genomics and Systems Biology, Department of Biology, NY, New York, 10003, USA.
  • Hutchison C; New York University, Center for Genomics and Systems Biology, Department of Biology, NY, New York, 10003, USA.
  • Desvoyes B; Centro de Biologia Molecular Severo Ochoa, 28049 Madrid, Spain.
  • Gutierrez C; Centro de Biologia Molecular Severo Ochoa, 28049 Madrid, Spain.
  • Birnbaum KD; New York University, Center for Genomics and Systems Biology, Department of Biology, NY, New York, 10003, USA.
bioRxiv ; 2024 Oct 15.
Article em En | MEDLINE | ID: mdl-38168452
ABSTRACT
The plasticity of plant cells underlies their wide capacity to regenerate, with increasing evidence in plants and animals implicating cell cycle dynamics in cellular reprogramming. To investigate the cell cycle during cellular reprogramming, we developed a comprehensive set of cell cycle phase markers in the Arabidopsis root. Using single-cell RNA-seq profiles and live imaging during regeneration, we found that a subset of cells near an ablation injury dramatically increases division rate by truncating G1. Cells in G1 undergo a transient nuclear peak of glutathione (GSH) prior to coordinated entry into S phase followed by rapid divisions and cellular reprogramming. A symplastic block of the ground tissue impairs regeneration, which is rescued by exogenous GSH. We propose a model in which GSH from the outer tissues is released upon injury licensing an exit from G1 near the wound to induce rapid cell division and reprogramming.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos