Abstract
PIN-FORMED (PIN) proteins localize asymmetrically at the plasma membrane and mediate intercellular polar transport of the plant hormone auxin that is crucial for a multitude of developmental processes in plants. PIN localization is under extensive control by environmental or developmental cues, but mechanisms regulating PIN localization are not fully understood. Here we show that early endosomal components ARF GEF BEN1 and newly identified Sec1/Munc18 family protein BEN2 are involved in distinct steps of early endosomal trafficking. BEN1 and BEN2 are collectively required for polar PIN localization, for their dynamic repolarization, and consequently for auxin activity gradient formation and auxin-related developmental processes including embryonic patterning, organogenesis, and vasculature venation patterning. These results show that early endosomal trafficking is crucial for cell polarity and auxin-dependent regulation of plant architecture.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alcohol Oxidoreductases / genetics*
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Alcohol Oxidoreductases / metabolism
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Arabidopsis / genetics*
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Arabidopsis / growth & development
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Arabidopsis Proteins / genetics*
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Arabidopsis Proteins / metabolism
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Biological Transport
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Cell Membrane / genetics
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Cell Membrane / metabolism
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Cell Polarity / genetics*
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Cytoplasmic Dyneins / genetics*
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Endosomes / genetics
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Endosomes / metabolism
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Gene Expression Regulation, Plant
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Indoleacetic Acids / metabolism
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Munc18 Proteins / genetics*
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Munc18 Proteins / metabolism
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Plant Roots / genetics
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Plant Roots / metabolism
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Protein Transport / genetics
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Transport Vesicles / genetics
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Transport Vesicles / metabolism
Substances
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Arabidopsis Proteins
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Indoleacetic Acids
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Munc18 Proteins
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Alcohol Oxidoreductases
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BEN1 protein, Arabidopsis
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DYNLL1 protein, human
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Cytoplasmic Dyneins
Grants and funding
This work was supported by the European Research Council with a Starting Independent Research grant (ERC-2011-StG-20101109-PSDP to JF); MEXT and JSPS KAKENHI (23012026 and 23770147 to HT); International Human Frontier Science Program (HFSP CDA to HT); and Vetenskapsråde, VINNOVA, and the K&A Wallenberg Foundation (to SR). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.