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The plasma membrane recycling pathway and cell polarity in plants: studies on PIN proteins
Author(s) -
Yohann Boutté,
MarieThérèse Crosnier,
Nicola Carraro,
Jan Traas,
Béatrice SatiatJeunemaître
Publication year - 2006
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.02847
Subject(s) - biology , endomembrane system , microbiology and biotechnology , microtubule , cytoskeleton , cytokinesis , golgi apparatus , cell plate , context (archaeology) , cell polarity , cytoplasm , transport protein , organelle , actin cytoskeleton , actin , membrane protein , cell , endoplasmic reticulum , biochemistry , membrane , cell division , paleontology
The PIN-FORMED (PIN) proteins are plasma-membrane-associated facilitators of auxin transport. They are often targeted to one side of the cell only through subcellular mechanisms that remain largely unknown. Here, we have studied the potential roles of the cytoskeleton and endomembrane system in the localisation of PIN proteins. Immunocytochemistry and image analysis on root cells from Arabidopsis thaliana and maize showed that 10-30% of the intracellular PIN proteins mapped to the Golgi network, but never to prevacuolar compartments. The remaining 70-90% were associated with yet to be identified structures. The maintenance of PIN proteins at the plasma membrane depends on a BFA-sensitive machinery, but not on microtubules and actin filaments. The polar localisation of PIN proteins at the plasmamembrane was not reflected by any asymmetric distribution of cytoplasmic organelles. In addition, PIN proteins were inserted in a symmetrical manner at both sides of the cell plate during cytokinesis. Together, the data indicate that the localisation of PIN proteins is a postmitotic event, which depends on local characteristics of the plasma membrane and its direct environment. In this context, we present evidence that microtubule arrays might define essential positional information for PIN localisation. This information seems to require the presence of an intact cell wall.

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