Cargando…

Evolutionary Adaptations of Plant AGC Kinases: From Light Signaling to Cell Polarity Regulation

Signaling and trafficking over membranes involves a plethora of transmembrane proteins that control the flow of compounds or relay specific signaling events. Next to external cues, internal stimuli can modify the activity or abundance of these proteins at the plasma membrane (PM). One such regulator...

Descripción completa

Detalles Bibliográficos
Autores principales: Rademacher, Eike H., Offringa, Remko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499706/
https://www.ncbi.nlm.nih.gov/pubmed/23162562
http://dx.doi.org/10.3389/fpls.2012.00250
_version_ 1782250004199505920
author Rademacher, Eike H.
Offringa, Remko
author_facet Rademacher, Eike H.
Offringa, Remko
author_sort Rademacher, Eike H.
collection PubMed
description Signaling and trafficking over membranes involves a plethora of transmembrane proteins that control the flow of compounds or relay specific signaling events. Next to external cues, internal stimuli can modify the activity or abundance of these proteins at the plasma membrane (PM). One such regulatory mechanism is protein phosphorylation by membrane-associated kinases, several of which are AGC kinases. The AGC kinase family is one of seven kinase families that are conserved in all eukaryotic genomes. In plants evolutionary adaptations introduced specific structural changes within the AGC kinases that most likely allow modulation of kinase activity by external stimuli (e.g., light). Starting from the well-defined structural basis common to all AGC kinases we review the current knowledge on the structure-function relationship in plant AGC kinases. Nine of the 39 Arabidopsis AGC kinases have now been shown to be involved in the regulation of auxin transport. In particular, AGC kinase-mediated phosphorylation of the auxin transporters ABCB1 and ABCB19 has been shown to regulate their activity, while auxin transporters of the PIN family are located to different positions at the PM depending on their phosphorylation status, which is a result of counteracting AGC kinase and PP6 phosphatase activities. We therefore focus on regulation of AGC kinase activity in this context. Identified structural adaptations of the involved AGC kinases may provide new insight into AGC kinase functionality and demonstrate their position as central hubs in the cellular network controlling plant development and growth.
format Online
Article
Text
id pubmed-3499706
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-34997062012-11-16 Evolutionary Adaptations of Plant AGC Kinases: From Light Signaling to Cell Polarity Regulation Rademacher, Eike H. Offringa, Remko Front Plant Sci Plant Science Signaling and trafficking over membranes involves a plethora of transmembrane proteins that control the flow of compounds or relay specific signaling events. Next to external cues, internal stimuli can modify the activity or abundance of these proteins at the plasma membrane (PM). One such regulatory mechanism is protein phosphorylation by membrane-associated kinases, several of which are AGC kinases. The AGC kinase family is one of seven kinase families that are conserved in all eukaryotic genomes. In plants evolutionary adaptations introduced specific structural changes within the AGC kinases that most likely allow modulation of kinase activity by external stimuli (e.g., light). Starting from the well-defined structural basis common to all AGC kinases we review the current knowledge on the structure-function relationship in plant AGC kinases. Nine of the 39 Arabidopsis AGC kinases have now been shown to be involved in the regulation of auxin transport. In particular, AGC kinase-mediated phosphorylation of the auxin transporters ABCB1 and ABCB19 has been shown to regulate their activity, while auxin transporters of the PIN family are located to different positions at the PM depending on their phosphorylation status, which is a result of counteracting AGC kinase and PP6 phosphatase activities. We therefore focus on regulation of AGC kinase activity in this context. Identified structural adaptations of the involved AGC kinases may provide new insight into AGC kinase functionality and demonstrate their position as central hubs in the cellular network controlling plant development and growth. Frontiers Media S.A. 2012-11-16 /pmc/articles/PMC3499706/ /pubmed/23162562 http://dx.doi.org/10.3389/fpls.2012.00250 Text en Copyright © 2012 Rademacher and Offringa. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Plant Science
Rademacher, Eike H.
Offringa, Remko
Evolutionary Adaptations of Plant AGC Kinases: From Light Signaling to Cell Polarity Regulation
title Evolutionary Adaptations of Plant AGC Kinases: From Light Signaling to Cell Polarity Regulation
title_full Evolutionary Adaptations of Plant AGC Kinases: From Light Signaling to Cell Polarity Regulation
title_fullStr Evolutionary Adaptations of Plant AGC Kinases: From Light Signaling to Cell Polarity Regulation
title_full_unstemmed Evolutionary Adaptations of Plant AGC Kinases: From Light Signaling to Cell Polarity Regulation
title_short Evolutionary Adaptations of Plant AGC Kinases: From Light Signaling to Cell Polarity Regulation
title_sort evolutionary adaptations of plant agc kinases: from light signaling to cell polarity regulation
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499706/
https://www.ncbi.nlm.nih.gov/pubmed/23162562
http://dx.doi.org/10.3389/fpls.2012.00250
work_keys_str_mv AT rademachereikeh evolutionaryadaptationsofplantagckinasesfromlightsignalingtocellpolarityregulation
AT offringaremko evolutionaryadaptationsofplantagckinasesfromlightsignalingtocellpolarityregulation