内复制
生物
有丝分裂
细胞周期蛋白依赖激酶
激酶
细胞生物学
细胞周期蛋白依赖激酶4
拟南芥
细胞周期蛋白
细胞周期
细胞周期蛋白依赖激酶6
细胞周期蛋白依赖激酶2
蛋白激酶A
遗传学
基因
突变体
作者
Aurine Verkest,Carmem-Lara de O. Manes,Steven Vercruysse,Sara Maes,Els Van Der Schueren,Tom Beeckman,Pascal Genschik,Martin Kuiper,Dirk Inzé,Lieven De Veylder
出处
期刊:The Plant Cell
[Oxford University Press]
日期:2005-04-29
卷期号:17 (6): 1723-1736
被引量:276
标识
DOI:10.1105/tpc.105.032383
摘要
Abstract Exit from the mitotic cell cycle and initiation of cell differentiation frequently coincides with the onset of endoreduplication, a modified cell cycle during which DNA continues to be duplicated in the absence of mitosis. Although the mitotic cell cycle and the endoreduplication cycle share much of the same machinery, the regulatory mechanisms controlling the transition between both cycles remain poorly understood. We show that the A-type cyclin-dependent kinase CDKA;1 and its specific inhibitor, the Kip-related protein, KRP2 regulate the mitosis-to-endocycle transition during Arabidopsis thaliana leaf development. Constitutive overexpression of KRP2 slightly above its endogenous level only inhibited the mitotic cell cycle–specific CDKA;1 kinase complexes, whereas the endoreduplication cycle-specific CDKA;1 complexes were unaffected, resulting in an increase in the DNA ploidy level. An identical effect on the endoreduplication cycle could be observed by overexpressing KRP2 exclusively in mitotically dividing cells. In agreement with a role for KRP2 as activator of the mitosis-to-endocycle transition, KRP2 protein levels were more abundant in endoreduplicating than in mitotically dividing tissues. We illustrate that KRP2 protein abundance is regulated posttranscriptionally through CDK phosphorylation and proteasomal degradation. KRP2 phosphorylation by the mitotic cell cycle–specific CDKB1;1 kinase suggests a mechanism in which CDKB1;1 controls the level of CDKA;1 activity through regulating KRP2 protein abundance. In accordance with this model, KRP2 protein levels increased in plants with reduced CDKB1;1 activity. Moreover, the proposed model allowed a dynamical simulation of the in vivo observations, validating the sufficiency of the regulatory interactions between CDKA;1, KRP2, and CDKB1;1 in fine-tuning the mitosis-to-endocycle transition.
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