The Arabidopsis GRAS-type SCL28 transcription factor controls the mitotic cell cycle and division plane orientation
Gene expression is reconfigured rapidly during the cell cycle to execute the cellular functions specific to each phase. Studies conducted with synchronized plant cell suspension cultures have identified hundreds of genes with periodic expression patterns across the phases of the cell cycle, but thes...
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Published in: | Proceedings of the National Academy of Sciences - PNAS Vol. 118; no. 6; pp. 1 - 12 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
National Academy of Sciences
09-02-2021
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Subjects: | |
Online Access: | Get full text |
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Summary: | Gene expression is reconfigured rapidly during the cell cycle to execute the cellular functions specific to each phase. Studies conducted with synchronized plant cell suspension cultures have identified hundreds of genes with periodic expression patterns across the phases of the cell cycle, but these results may differ from expression occurring in the context of intact organs. Here, we describe the use of fluorescence-activated cell sorting to analyze the gene expression profile of G2/M cells in the growing root. To this end, we isolated cells expressing the early mitosis cell cycle marker CYCLINB1;1-GFP from Arabidopsis root tips. Transcriptome analysis of these cells allowed identification of hundreds of genes whose expression is reduced or enriched in G2/M cells, including many not previously reported from cell suspension cultures. From this dataset, we identified SCL28, a transcription factor belonging to the GRAS family, whose messenger RNA accumulates to the highest levels in G2/M and is regulated by MYB3R transcription factors. Functional analysis indicates that SCL28 promotes progression through G2/M and modulates the selection of cell division planes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author contributions: P.N.B., L.D.V., J.P., and R.E.R. designed research; C.G., J.-A.P.-G., N.B., T.C., R.V., and R.E.R. performed research; P.N.B., L.D.V., J.P., and R.E.R. contributed new reagents/analytic tools; C.G., J.-A.P.-G., R.V., and R.E.R. analyzed data; and C.G. and R.E.R. wrote the paper. Edited by Enrico Coen, John Innes Centre, Norwich, United Kingdom, and approved December 18, 2020 (received for review March 20, 2020) |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.2005256118 |