Elucidating the functional role of endoreduplication in tomato fruit development
Langue
en
Article de revue
Ce document a été publié dans
Annals of Botany. 2011, vol. 107, n° 7, p. 1159-1169
Oxford University Press (OUP)
Résumé en anglais
Background Endoreduplication is the major source of endopolyploidy in higher plants. The process of endoreduplication results from the ability of cells to modify their classical cell cycle into a partial cell cycle where ...Lire la suite >
Background Endoreduplication is the major source of endopolyploidy in higher plants. The process of endoreduplication results from the ability of cells to modify their classical cell cycle into a partial cell cycle where DNA synthesis occurs independently from mitosis. Despite the ubiquitous occurrence of the phenomenon in eukaryotic cells, the physiological meaning of endoreduplication remains vague,although several roles during plant development have been proposed, mostly related to cell differentiation and cell size determination. Scope Here recent advances in the knowledge of endoreduplication and fruit organogenesis are reviewed, focusing on tomato (Solanum lycopersicum) as a model, and the functional analyses of endoreduplication-associated regulatory genes in tomato fruit are described. Conclusions The cyclin-dependent kinase inhibitory kinase WEE1 and the anaphase promoting complex activator CCS52A both participate in the control of cell size and the endoreduplication process driving cell expansion during early fruit development in tomato. Moreover the fruit-specific functional analysis of the tomato CDK inhibitor KRP1 reveals that cell size and fruit size determination can be uncoupled from DNA ploidy levels, indicating that endoreduplication acts rather as a limiting factor for cell growth. The overall functional data contribute to unravelling the physiological role of endoreduplication in growth induction of fleshy fruits.< Réduire
Mots clés
CCS52A
BIOLOGIE DU DEVELOPPEMENT
BIOLOGIE MOLECULAIRE
BIOLOGIE VEGETALE
Mots clés en anglais
ANAPHASE PROMOTING COMPLEX
CDK INHIBITORS
CELL CYCLE CONTROL
WEE1 KINASE
CYCLIN-DEPENDENT KINASE
Origine
Importé de halUnités de recherche