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First published online March 2, 2006; 10.1104/pp.106.077990

Plant Physiology 140:1355-1366 (2006)
© 2006 American Society of Plant Biologists

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SYSTEMS BIOLOGY, MOLECULAR BIOLOGY, AND GENE REGULATION

Interplay between Arabidopsis Activating Factors E2Fb and E2Fa in Cell Cycle Progression and Development1,[W]

Rosangela Sozzani, Caterina Maggio, Serena Varotto, Sabrina Canova, Catherine Bergounioux, Diego Albani and Rino Cella*

Department of Genetics and Microbiology, University of Pavia, 27100 Pavia, Italy (R.S., C.M., R.C.); Department of Environmental Agronomy and Crop Production, University of Padova, Agripolis, 35020 Legnaro, Italy (S.V., S.C.); Institute of Plant Biotechnology, University of Paris-XI, 91400 Orsay, France (C.B.); and Department of Botany and Plant Ecology, University of Sassari, 07100 Sassari, Italy (D.A.)

Eukaryotic E2Fs are conserved transcription factors playing crucial and antagonistic roles in several pathways related to cell division, DNA repair, and differentiation. In plants, these processes are strictly intermingled at the growing zone to produce postembryonic development in response to internal signals and environmental cues. Of the six AtE2F proteins found in Arabidopsis (Arabidopsis thaliana), only AtE2Fa and AtE2Fb have been clearly indicated as activators of E2F-responsive genes. AtE2Fa activity was shown to induce S phase and endoreduplication, whereas the function of AtE2Fb and the interrelationship between these two transcription factors was unclear. We have investigated the role played by the AtE2Fb gene during cell cycle and development performing in situ RNA hybridization, immunolocalization of the AtE2Fb protein in planta, and analysis of AtE2Fb promoter activity in transgenic plants. Overexpression of AtE2Fb in transgenic Arabidopsis plants led to striking modifications of the morphology of roots, cotyledons, and leaves that can be ascribed to stimulation of cell division. The accumulation of the AtE2Fb protein in these lines was paralleled by an increased expression of E2F-responsive G1/S and G2/M marker genes. These results suggest that AtE2Fa and AtE2Fb have specific expression patterns and play similar but distinct roles during cell cycle progression.


1 This work was supported by the Ministero dell'Istruzione, dell'Università e della Ricerca (grant nos. RBNE01TYZF–004 and PRIN 2004).

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Rino Cella (cella{at}ipvgen.unipv.it).

[W] The online version of this article contains Web-only data.

Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.106.077990.

* Corresponding author; e-mail cella{at}ipvgen.unipv.it; fax 39–0382–528496.

Received January 27, 2006; returned for revision February 13, 2006; accepted February 14, 2006.




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