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Interactions among PIN-FORMED and P-Glycoprotein Auxin Transporters in Arabidopsis
Author(s) -
Joshua J. Blakeslee,
Anindita Bandyopadhyay,
Ok Ran Lee,
Jozef Mravec,
Boosaree Titapiwatanakun,
Michael Sauer,
Srinivas N. Makam,
Yan Cheng,
Rodolphe Bouchard,
Jiří Adamec,
Markus Geisler,
Akitomo Nagashima,
Tatsuya Sakai,
Enrico Martinoia,
Jìří Friml,
Wendy Ann Peer,
Angus Murphy
Publication year - 2007
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.106.040782
Subject(s) - auxin , biology , arabidopsis , polar auxin transport , microbiology and biotechnology , heterologous expression , efflux , mutant , heterologous , arabidopsis thaliana , transporter , membrane transport protein , biochemistry , function (biology) , transport protein , immunoprecipitation , gene , recombinant dna
Directional transport of the phytohormone auxin is established primarily at the point of cellular efflux and is required for the establishment and maintenance of plant polarity. Studies in whole plants and heterologous systems indicate that PIN-FORMED (PIN) and P-glycoprotein (PGP) transport proteins mediate the cellular efflux of natural and synthetic auxins. However, aromatic anion transport resulting from PGP and PIN expression in nonplant systems was also found to lack the high level of substrate specificity seen in planta. Furthermore, previous reports that PGP19 stabilizes PIN1 on the plasma membrane suggested that PIN-PGP interactions might regulate polar auxin efflux. Here, we show that PGP1 and PGP19 colocalized with PIN1 in the shoot apex in Arabidopsis thaliana and with PIN1 and PIN2 in root tissues. Specific PGP-PIN interactions were seen in yeast two-hybrid and coimmunoprecipitation assays. PIN-PGP interactions appeared to enhance transport activity and, to a greater extent, substrate/inhibitor specificities when coexpressed in heterologous systems. By contrast, no interactions between PGPs and the AUXIN1 influx carrier were observed. Phenotypes of pin and pgp mutants suggest discrete functional roles in auxin transport, but pin pgp mutants exhibited phenotypes that are both additive and synergistic. These results suggest that PINs and PGPs characterize coordinated, independent auxin transport mechanisms but also function interactively in a tissue-specific manner.

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