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First published online March 13, 2009; 10.1104/pp.108.133918 Plant Physiology 150:105-113 (2009) © 2009 American Society of Plant Biologists The Arabidopsis Callose Synthase Gene GSL8 Is Required for Cytokinesis and Cell Patterning1,[C],[W]Division of Applied Life Science (BK21 Program), Graduate School of Gyeongsang National University, Plant Molecular Biology and Biotechnology Research Center, Environmental Biotechnology National Core Research Center, Jinju 660–701, Korea (X.-Y.C., L.L., X.H., Y.R., H.C., S.-W.K., J.-Y.K.); and Department of Botany, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z4 (E.L., F.S.)
Cytokinesis is the division of the cytoplasm and its separation into two daughter cells. Cell plate growth and cytokinesis appear to require callose, but direct functional evidence is still lacking. To determine the role of callose and its synthesis during cytokinesis, we identified and characterized mutants in many members of the GLUCAN SYNTHASE-LIKE (GSL; or CALLOSE SYNTHASE) gene family in Arabidopsis (Arabidopsis thaliana). Most gsl mutants (gsl1–gsl7, gsl9, gsl11, and gsl12) exhibited roughly normal seedling growth and development. However, mutations in GSL8, which were previously reported to be gametophytic lethal, were found to produce seedlings with pleiotropic defects during embryogenesis and early vegetative growth. We found cell wall stubs, two nuclei in one cell, and other defects in cell division in homozygous gsl8 insertional alleles. In addition, gsl8 mutants and inducible RNA interference lines of GSL8 showed reduced callose deposition at cell plates and/or new cell walls. Together, these data show that the GSL8 gene encodes a putative callose synthase required for cytokinesis and seedling maturation. In addition, gsl8 mutants disrupt cellular and tissue-level patterning, as shown by the presence of clusters of stomata in direct contact and by islands of excessive cell proliferation in the developing epidermis. Thus, GSL8 is required for patterning as well as cytokinesis during Arabidopsis development.
1 This work was supported by the Korea Research Foundation (grant no. C00239), by grants from Korea Science and Engineering Foundation/Ministry of Education, Science and Technology to the National Research Lab Program (grant no. M10600000205–06J0000–20510), the World Class University Program (grant no. R33–2008–000–1002–0), and the Environmental Biotechnology National Core Research Center (grant no. R15–2003–012–01003–0), by the Natural Sciences and Engineering Research Council of Canada (Discovery grant to F.D.S.), and by scholarships from the BK21 Program from the Ministry of Education, Science, and Technology, Korea, to X.-Y.C., X.H., Y.R., H.C., and L.L. 2 These authors contributed equally to the article. 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: Jae-Yean Kim (kimjy{at}gnu.ac.kr). [C] Some figures in this article are displayed in color online but in black and white in the print edition. [W] The online version of this article contains Web-only data. www.plantphysiol.org/cgi/doi/10.1104/pp.108.133918 * Corresponding author; e-mail kimjy{at}gnu.ac.kr. Received December 9, 2008; accepted March 10, 2009; published March 13, 2009.
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