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Click chemistry-based tracking reveals putative cell wall-located auxin binding sites in expanding cells
J. Mravec, SK. Kračun, E. Zemlyanskaya, MG. Rydahl, X. Guo, M. Pičmanová, KK. Sørensen, K. Růžička, WGT. Willats,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
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Directory of Open Access Journals
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- MeSH
- buněčná stěna metabolismus MeSH
- kyseliny indoloctové metabolismus MeSH
- rostlinné proteiny metabolismus MeSH
- syntetická chemie okamžité shody metody MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Auxin is a key plant regulatory molecule, which acts upon a plethora of cellular processes, including those related to cell differentiation and elongation. Despite the stunning progress in all disciplines of auxin research, the mechanisms of auxin-mediated rapid promotion of cell expansion and underlying rearrangement of cell wall components are poorly understood. This is partly due to the limitations of current methodologies for probing auxin. Here we describe a click chemistry-based approach, using an azido derivative of indole-3-propionic acid. This compound is as an active auxin analogue, which can be tagged in situ. Using this new tool, we demonstrate the existence of putative auxin binding sites in the cell walls of expanding/elongating cells. These binding sites are of protein nature but are distinct from those provided by the extensively studied AUXIN BINDING PROTEIN 1 (ABP1). Using immunohistochemistry, we have shown the apoplastic presence of endogenous auxin epitopes recognised by an anti-IAA antibody. Our results are intriguingly in line with previous observations suggesting some transcription-independent (non-genomic) activity of auxin in cell elongation.
CEITEC Masaryk University Kamenice 5 CZ 625 00 Brno Czechia
Department of Chemistry University of Copenhagen Thorvaldsensvej 40 1871 Frederiksberg C Denmark
Citace poskytuje Crossref.org
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- $a Mravec, Jozef $u Department of Plant and Environmental Sciences, University of Copenhagen, Thorvaldsensvej 40, 1871, Frederiksberg-C, Denmark. mravec@plen.ku.dk.
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- $a Click chemistry-based tracking reveals putative cell wall-located auxin binding sites in expanding cells / $c J. Mravec, SK. Kračun, E. Zemlyanskaya, MG. Rydahl, X. Guo, M. Pičmanová, KK. Sørensen, K. Růžička, WGT. Willats,
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- $a Auxin is a key plant regulatory molecule, which acts upon a plethora of cellular processes, including those related to cell differentiation and elongation. Despite the stunning progress in all disciplines of auxin research, the mechanisms of auxin-mediated rapid promotion of cell expansion and underlying rearrangement of cell wall components are poorly understood. This is partly due to the limitations of current methodologies for probing auxin. Here we describe a click chemistry-based approach, using an azido derivative of indole-3-propionic acid. This compound is as an active auxin analogue, which can be tagged in situ. Using this new tool, we demonstrate the existence of putative auxin binding sites in the cell walls of expanding/elongating cells. These binding sites are of protein nature but are distinct from those provided by the extensively studied AUXIN BINDING PROTEIN 1 (ABP1). Using immunohistochemistry, we have shown the apoplastic presence of endogenous auxin epitopes recognised by an anti-IAA antibody. Our results are intriguingly in line with previous observations suggesting some transcription-independent (non-genomic) activity of auxin in cell elongation.
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