Polar transport of the plant hormone auxin is controlled by PIN- and ABCB/PGP-efflux catalysts. PIN polarity is regulated by the AGC protein kinase, PINOID (PID), while ABCB activity was shown to be dependent on interaction with the FKBP42, TWISTED DWARF1 (TWD1). Using co-immunoprecipitation (co-IP) and shotgun LC–MS/MS analysis, we identified PID as a valid partner in the interaction with TWD1. In-vitro and yeast expression analyses indicated that PID specifically modulates ABCB1-mediated auxin efflux in an action that is dependent on its kinase activity and that is reverted by quercetin binding and thus inhibition of PID autophosphorylation. Triple ABCB1/PID/TWD1 co-transfection in tobacco revealed that PID enhances ABCB1-mediated auxin efflux but blocks ABCB1 in the presence of TWD1. Phospho-proteomic analyses identified S634 as a key residue of the regulatory ABCB1 linker and a very likely target of PID phosphorylation that determines both transporter drug binding and activity. In summary, we provide evidence that PID phosphorylation has a dual, counter-active impact on ABCB1 activity that is coordinated by TWD1–PID interaction.

Regulation of ABCB1/PGP1-catalysed auxin transport by linker phosphorylation / Sina Henrichs;Bangjun Wang;Yoichiro Fukao;Jinsheng Zhu;Laurence Charrier;Aurélien Bailly;Sophie C Oehring;Miriam Linnert;Matthias Weiwad;Anne Endler;Paolo Nanni;Stephan Pollmann;Stefano Mancuso;Alexander Schulz;Markus Geisler. - In: EMBO JOURNAL. - ISSN 1460-2075. - STAMPA. - 31:(2012), pp. 2965-2980. [10.1038/emboj.2012.120]

Regulation of ABCB1/PGP1-catalysed auxin transport by linker phosphorylation

MANCUSO, STEFANO;
2012

Abstract

Polar transport of the plant hormone auxin is controlled by PIN- and ABCB/PGP-efflux catalysts. PIN polarity is regulated by the AGC protein kinase, PINOID (PID), while ABCB activity was shown to be dependent on interaction with the FKBP42, TWISTED DWARF1 (TWD1). Using co-immunoprecipitation (co-IP) and shotgun LC–MS/MS analysis, we identified PID as a valid partner in the interaction with TWD1. In-vitro and yeast expression analyses indicated that PID specifically modulates ABCB1-mediated auxin efflux in an action that is dependent on its kinase activity and that is reverted by quercetin binding and thus inhibition of PID autophosphorylation. Triple ABCB1/PID/TWD1 co-transfection in tobacco revealed that PID enhances ABCB1-mediated auxin efflux but blocks ABCB1 in the presence of TWD1. Phospho-proteomic analyses identified S634 as a key residue of the regulatory ABCB1 linker and a very likely target of PID phosphorylation that determines both transporter drug binding and activity. In summary, we provide evidence that PID phosphorylation has a dual, counter-active impact on ABCB1 activity that is coordinated by TWD1–PID interaction.
2012
31
2965
2980
Sina Henrichs;Bangjun Wang;Yoichiro Fukao;Jinsheng Zhu;Laurence Charrier;Aurélien Bailly;Sophie C Oehring;Miriam Linnert;Matthias Weiwad;Anne Endler;Paolo Nanni;Stephan Pollmann;Stefano Mancuso;Alexander Schulz;Markus Geisler
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/651334
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