
AbstractMean cell size at division is generally constant for specific conditions and cell types, but the mechanisms coupling cell growth and cell cycle control with cell size regulation are poorly understood in intact tissues. Here we show that the continuously dividing fields of cells within the shoot apical meristem of Arabidopsis show dynamic regulation of mean cell size dependent on developmental stage, genotype and environmental signals. We show cell size at division and cell cycle length is effectively predicted using a two-stage cell cycle model linking cell growth and two sequential cyclin dependent kinase (CDK) activities, and experimental results concur in showing that progression through both G1/S and G2/M is size dependent. This work shows that cell-autonomous co-ordination of cell growth and cell division previously observed in unicellular organisms also exists in intact plant tissues, and that cell size may be an emergent rather than directly determined property of cells.
570, [SDV]Life Sciences [q-bio], Science, Meristem, 610, Article, Gene Expression Regulation, Plant, Plant Cells, homeostasis, Homeostasis, homéostasie, Cell Size, Plant Proteins, cell division cycle, flexibilité, Models, Genetic, cellule végétale, Q, Cell Cycle, Gene Expression Regulation, Developmental, pliability, cycle cellulaire, Cyclin-Dependent Kinases, [SDV] Life Sciences [q-bio], arabidopsis, plant cells, Cell Division, Plant Shoots
570, [SDV]Life Sciences [q-bio], Science, Meristem, 610, Article, Gene Expression Regulation, Plant, Plant Cells, homeostasis, Homeostasis, homéostasie, Cell Size, Plant Proteins, cell division cycle, flexibilité, Models, Genetic, cellule végétale, Q, Cell Cycle, Gene Expression Regulation, Developmental, pliability, cycle cellulaire, Cyclin-Dependent Kinases, [SDV] Life Sciences [q-bio], arabidopsis, plant cells, Cell Division, Plant Shoots
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 124 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 1% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |
