RETINOBLASTOMA RELATED1 Regulates Asymmetric Cell Divisions in Arabidopsis
Author(s) -
Annika K. Weimer,
Moritz K. Nowack,
Daniel Bouyer,
Xin’Ai Zhao,
Hirofumi Harashima,
Sadaf Naseer,
Freya De Winter,
Nico Dißmeyer,
Niko Geldner,
Arp Schnittger
Publication year - 2012
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.112.104620
Subject(s) - biology , cyclin dependent kinase , arabidopsis , microbiology and biotechnology , cell cycle , retinoblastoma protein , cell fate determination , e2f , cyclin dependent kinase 1 , cell division , asymmetric cell division , formative assessment , genetics , transcription factor , gene , cell , mutant , statistics , mathematics
Formative, also called asymmetric, cell divisions produce daughter cells with different identities. Like other divisions, formative divisions rely first of all on the cell cycle machinery with centrally acting cyclin-dependent kinases (CDKs) and their cyclin partners to control progression through the cell cycle. However, it is still largely obscure how developmental cues are translated at the cellular level to promote asymmetric divisions. Here, we show that formative divisions in the shoot and root of the flowering plant Arabidopsis thaliana are controlled by a common mechanism that relies on the activity level of the Cdk1 homolog CDKA;1, with medium levels being sufficient for symmetric divisions but high levels being required for formative divisions. We reveal that the function of CDKA;1 in asymmetric cell divisions operates through a transcriptional regulation system that is mediated by the Arabidopsis Retinoblastoma homolog RBR1. RBR1 regulates not only cell cycle genes, but also, independent of the cell cycle transcription factor E2F, genes required for formative divisions and cell fate acquisition, thus directly linking cell proliferation with differentiation. This mechanism allows the implementation of spatial information, in the form of high kinase activity, with intracellular gating of developmental decisions.
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