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First published online 3 October 2007
doi: 10.1242/dev.009654
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1 Graduate School of Biological Sciences, Nara Institute of Science and
Technology, Nara 630-0101, Japan.
2 Lehrstuhl für Genetik, Technische Universität München,
Wissenschaftszentrum Weihenstephan, Am Hochanger 8, 85350 Freising,
Germany.
Author for correspondence (e-mail:
m-tasaka{at}bs.naist.jp)
Accepted 10 August 2007
Intercellular transport of the phytohormone auxin is a significant factor for plant organogenesis. To investigate molecular mechanisms by which auxin controls organogenesis, we analyzed the macchi-bou 4 (mab4) mutant identified as an enhancer of pinoid (pid). Although mab4 and pid single mutants displayed relatively mild cotyledon phenotypes, pid mab4 double mutants completely lacked cotyledons. We found that MAB4 was identical to ENHANCER OF PINOID (ENP), which has been suggested to control PIN1 polarity in cotyledon primordia. MAB4/ENP encodes a novel protein, which belongs to the NON-PHOTOTROPIC HYPOCOTYL 3 (NPH3) family thought to function as a signal transducer in phototropism and control lateral translocation of auxin. MAB4/ENP mRNA was detected in the protodermal cell layer of the embryo and the meristem L1 layer at the site of organ initiation. In the mab4 embryo, the abundance of PIN1:GFP was severely decreased at the plasma membrane in the protodermal cell layer. In addition, subcellular localization analyses indicated that MAB4/ENP resides on a subpopulation of endosomes as well as on unidentified intracellular compartments. These results indicate that MAB4/ENP is involved in polar auxin transport in organogenesis.
Key words: Polar auxin transport, Organ development, PIN1, PID, NPH3, Arabidopsis thaliana
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