Edinburgh, Scotland, United Kingdom - TAIR
Edinburgh, Scotland, United Kingdom - TAIR
Edinburgh, Scotland, United Kingdom - TAIR
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Small GTPases in post-Golgi and endocytic<br />
membrane traffic in Arabidopsis<br />
The endomembrane organelles and their associated trafficking pathways<br />
synthesise some of the most biologically and commercially important structures<br />
in plants. Circumstantial evidence suggests that intracellular membrane trafficking<br />
pathways diversified independently in the plant kingdom but documented<br />
examples are rare. Rab GTPases are essential regulators of membrane identity<br />
and membrane targeting specificity in eukaryotic cells. Rab GTPase families<br />
have diversified independently in the animal and plant lineages. We show that<br />
in Arabidopsis root tips, the Rab-A2 and Rab-A3 subclasses define a novel post-<br />
Golgi membrane domain that communicates with the plasma membrane and<br />
early endosomal system and contributes substantially to the cell plate during<br />
cytokinesis. In contrast to the Rab-A2 and –A3 subclasses, Rab-A5 proteins<br />
define compartments with a distinct and apparently unique distribution at the<br />
periphery of root meristematic cells.<br />
We have also employed a screen based on accumulation of secreted GFP to<br />
identify mutations that affect biosynthetic membrane traffic in Arabidopsis. Using<br />
this screen we identified mutants in the GBF-family Arf GEF GNOM-LIKE1<br />
(GNL1). We show that GNL1 is a BFA-resistant GBF protein that functions<br />
together with a BFA-sensitive Arf GEF both at the Golgi and in endocytic<br />
trafficking of PIN2 but not of other plasma-membrane markers. The evolution of<br />
endocytic trafficking in plants was apparently accompanied by neofunctionalisation<br />
within the GBF family while in other kingdoms it occurred independently<br />
by elaboration of additional Arf GEF families. A TILLING screen of additional<br />
seedling-lethal secretory mutants suggests that several will identify components<br />
of the trafficking machinery that are not previously well characterised.<br />
41<br />
L16<br />
Friday 11:00 - 11:30<br />
Cell Biology<br />
Ian Moore<br />
University of Oxford<br />
UK