| Literature DB >> 32753430 |
Constance Musseau1, Joana Jorly1, Stéphanie Gadin1, Iben Sørensen2, Catherine Deborde1,3, Stéphane Bernillon1,3, Jean-Philippe Mauxion1, Isabelle Atienza1, Annick Moing1,3, Martine Lemaire-Chamley1, Jocelyn K C Rose2, Christian Chevalier1, Christophe Rothan1, Lucie Fernandez-Lochu4, Frédéric Gévaudant1.
Abstract
Cell fate maintenance is an integral part of plant cell differentiation and the production of functional cells, tissues, and organs. Fleshy fruit development is characterized by the accumulation of water and solutes in the enlarging cells of parenchymatous tissues. In tomato (Solanum lycopersicum), this process is associated with endoreduplication in mesocarp cells. The mechanisms that preserve this developmental program, once initiated, remain unknown. We show here that analysis of a previously identified tomato ethyl methanesulfonate-induced mutant that exhibits abnormal mesocarp cell differentiation could help elucidate determinants of fruit cell fate maintenance. We identified and validated the causal locus through mapping-by-sequencing and gene editing, respectively, and performed metabolic, cellular, and transcriptomic analyses of the mutant phenotype. The data indicate that disruption of the SlGBP1 gene, encoding GUANYLATE BINDING PROTEIN1, induces early termination of endoreduplication followed by late divisions of polyploid mesocarp cells, which consequently acquire the characteristics of young proliferative cells. This study reveals a crucial role of plant GBPs in the control of cell cycle genes, and thus, in cell fate maintenance. We propose that SlGBP1 acts as an inhibitor of cell division, a function conserved with the human hGBP-1 protein.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32753430 PMCID: PMC7534463 DOI: 10.1105/tpc.20.00245
Source DB: PubMed Journal: Plant Cell ISSN: 1040-4651 Impact factor: 11.277