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Systems approaches reveal that ABCB and PIN proteins mediate co-dependent auxin efflux

Members of the B family of membrane-bound ATP-binding cassette (ABC) transporters represent key components of the auxin efflux machinery in plants. Over the last two decades, experimental studies have shown that modifying ATP-binding cassette sub-family B (ABCB) expression affects auxin distribution...

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Autores principales: Mellor, Nathan L, Voß, Ute, Ware, Alexander, Janes, George, Barrack, Duncan, Bishopp, Anthony, Bennett, Malcolm J, Geisler, Markus, Wells, Darren M, Band, Leah R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134068/
https://www.ncbi.nlm.nih.gov/pubmed/35302640
http://dx.doi.org/10.1093/plcell/koac086
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author Mellor, Nathan L
Voß, Ute
Ware, Alexander
Janes, George
Barrack, Duncan
Bishopp, Anthony
Bennett, Malcolm J
Geisler, Markus
Wells, Darren M
Band, Leah R
author_facet Mellor, Nathan L
Voß, Ute
Ware, Alexander
Janes, George
Barrack, Duncan
Bishopp, Anthony
Bennett, Malcolm J
Geisler, Markus
Wells, Darren M
Band, Leah R
author_sort Mellor, Nathan L
collection PubMed
description Members of the B family of membrane-bound ATP-binding cassette (ABC) transporters represent key components of the auxin efflux machinery in plants. Over the last two decades, experimental studies have shown that modifying ATP-binding cassette sub-family B (ABCB) expression affects auxin distribution and plant phenotypes. However, precisely how ABCB proteins transport auxin in conjunction with the more widely studied family of PIN-formed (PIN) auxin efflux transporters is unclear, and studies using heterologous systems have produced conflicting results. Here, we integrate ABCB localization data into a multicellular model of auxin transport in the Arabidopsis thaliana root tip to predict how ABCB-mediated auxin transport impacts organ-scale auxin distribution. We use our model to test five potential ABCB–PIN regulatory interactions, simulating the auxin dynamics for each interaction and quantitatively comparing the predictions with experimental images of the DII-VENUS auxin reporter in wild-type and abcb single and double loss-of-function mutants. Only specific ABCB–PIN regulatory interactions result in predictions that recreate the experimentally observed DII-VENUS distributions and long-distance auxin transport. Our results suggest that ABCBs enable auxin efflux independently of PINs; however, PIN-mediated auxin efflux is predominantly through a co-dependent efflux where co-localized with ABCBs.
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spelling pubmed-91340682022-05-27 Systems approaches reveal that ABCB and PIN proteins mediate co-dependent auxin efflux Mellor, Nathan L Voß, Ute Ware, Alexander Janes, George Barrack, Duncan Bishopp, Anthony Bennett, Malcolm J Geisler, Markus Wells, Darren M Band, Leah R Plant Cell Research Articles Members of the B family of membrane-bound ATP-binding cassette (ABC) transporters represent key components of the auxin efflux machinery in plants. Over the last two decades, experimental studies have shown that modifying ATP-binding cassette sub-family B (ABCB) expression affects auxin distribution and plant phenotypes. However, precisely how ABCB proteins transport auxin in conjunction with the more widely studied family of PIN-formed (PIN) auxin efflux transporters is unclear, and studies using heterologous systems have produced conflicting results. Here, we integrate ABCB localization data into a multicellular model of auxin transport in the Arabidopsis thaliana root tip to predict how ABCB-mediated auxin transport impacts organ-scale auxin distribution. We use our model to test five potential ABCB–PIN regulatory interactions, simulating the auxin dynamics for each interaction and quantitatively comparing the predictions with experimental images of the DII-VENUS auxin reporter in wild-type and abcb single and double loss-of-function mutants. Only specific ABCB–PIN regulatory interactions result in predictions that recreate the experimentally observed DII-VENUS distributions and long-distance auxin transport. Our results suggest that ABCBs enable auxin efflux independently of PINs; however, PIN-mediated auxin efflux is predominantly through a co-dependent efflux where co-localized with ABCBs. Oxford University Press 2022-03-18 /pmc/articles/PMC9134068/ /pubmed/35302640 http://dx.doi.org/10.1093/plcell/koac086 Text en © American Society of Plant Biologists 2022. All rights reserved. For permissions, please email: journals.permissions@oup.com https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Mellor, Nathan L
Voß, Ute
Ware, Alexander
Janes, George
Barrack, Duncan
Bishopp, Anthony
Bennett, Malcolm J
Geisler, Markus
Wells, Darren M
Band, Leah R
Systems approaches reveal that ABCB and PIN proteins mediate co-dependent auxin efflux
title Systems approaches reveal that ABCB and PIN proteins mediate co-dependent auxin efflux
title_full Systems approaches reveal that ABCB and PIN proteins mediate co-dependent auxin efflux
title_fullStr Systems approaches reveal that ABCB and PIN proteins mediate co-dependent auxin efflux
title_full_unstemmed Systems approaches reveal that ABCB and PIN proteins mediate co-dependent auxin efflux
title_short Systems approaches reveal that ABCB and PIN proteins mediate co-dependent auxin efflux
title_sort systems approaches reveal that abcb and pin proteins mediate co-dependent auxin efflux
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134068/
https://www.ncbi.nlm.nih.gov/pubmed/35302640
http://dx.doi.org/10.1093/plcell/koac086
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