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Published December 30, 2014 | Supplemental Material + Published
Journal Article Open

Auxin depletion from leaf primordia contributes to organ patterning

Abstract

Stem cells are responsible for organogenesis, but it is largely unknown whether and how information from stem cells acts to direct organ patterning after organ primordia are formed. It has long been proposed that the stem cells at the plant shoot apex produce a signal, which promotes leaf adaxial-abaxial (dorsoventral) patterning. Here we show the existence of a transient low auxin zone in the adaxial domain of early leaf primordia. We also demonstrate that this adaxial low auxin domain contributes to leaf adaxial-abaxial patterning. The auxin signal is mediated by the auxin-responsive transcription factor MONOPTEROS (MP), whose constitutive activation in the adaxial domain promotes abaxial cell fate. Furthermore, we show that auxin flow from emerging leaf primordia to the shoot apical meristem establishes the low auxin zone, and that this auxin flow contributes to leaf polarity. Our results provide an explanation for the hypothetical meristem-derived leaf polarity signal. Opposite to the original proposal, instead of a signal derived from the meristem, we show that a signaling molecule is departing from the primordium to the meristem to promote robustness in leaf patterning.

Additional Information

Copyright © 2014 National Academy of Sciences. Contributed by Elliot Meyerowitz, November 20, 2014 (sent for review August 14, 2014; reviewed by Yuval Eshed and Lars Østergaard) Published online before print December 15, 2014, doi: 10.1073/pnas.1421878112 We thank Drs. N. Ori, E. A. Schultz, and D. Weijers for seeds; Dr. C. Li for allowing us to use his tomato growth facility; and Drs. Y. Eshed, H. Huang, C. Kuhlemeier, O. Leyser, and L. Xu for discussions. Y.J. thanks Profs. S.-N. Bai and Z.-H. Xu for their encouragement. This work was supported by National Basic Research Program of China (973 Program) Grant 2014CB943500, National Natural Science Foundation of China Grant 31222033, State Key Laboratory of Plant Genomics Grant SKLPG2011B0103, US National Science Foundation 2010 Project Grant MCB-0929349, and France ANR-12-BSV6-0005 Grant (AuxiFlo). The E.M. laboratory is also supported by funds from the Howard Hughes Medical Institute and Gordon and Betty Moore Foundation Grant GBMF3406, and the Y.J. laboratory is supported by the Hundred Talents Program of the Chinese Academy of Sciences. J.Q. and Y.W. contributed equally to this work. Author contributions: J.Q., Y.W., T.Y., B.W., and T.V. performed research; Y.W., E.M., and Y.J. designed research; A.C. and T.V. contributed new reagents/analytic tools; J.Q., Y.W., A.C., T.V., E.M., and Y.J. analyzed data; and T.V., E.M., and Y.J. wrote the paper. Reviewers: Y.E., Weizmann Institute of Science; and L.Ø., John Innes Centre. The authors declare no conflict of interest. This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1421878112/-/DCSupplemental.

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Published - 18769.full.pdf

Supplemental Material - pnas.201421878SI.pdf

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August 22, 2023
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