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A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis.


ABSTRACT: The coupling of endocytosis and exocytosis underlies fundamental biological processes ranging from fertilization to neuronal activity and cellular polarity. However, the mechanisms governing the spatial organization of endocytosis and exocytosis require clarification. Using a quantitative imaging-based screen in budding yeast, we identified 89 mutants displaying defects in the localization of either one or both pathways. High-resolution single-vesicle tracking revealed that the endocytic and exocytic mutants she4? and bud6? alter post-Golgi vesicle dynamics in opposite ways. The endocytic and exocytic pathways display strong interdependence during polarity establishment while being more independent during polarity maintenance. Systems analysis identified the exocyst complex as a key network hub, rich in genetic interactions with endocytic and exocytic components. Exocyst mutants displayed altered endocytic and post-Golgi vesicle dynamics and interspersed endocytic and exocytic domains compared with control cells. These data are consistent with an important role for the exocyst in coordinating endocytosis and exocytosis.

SUBMITTER: Jose M 

PROVIDER: S-EPMC4571305 | biostudies-literature | 2015 Jul

REPOSITORIES: biostudies-literature

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A quantitative imaging-based screen reveals the exocyst as a network hub connecting endocytosis and exocytosis.

Jose Mini M   Tollis Sylvain S   Nair Deepak D   Mitteau Romain R   Velours Christophe C   Massoni-Laporte Aurelie A   Royou Anne A   Sibarita Jean-Baptiste JB   McCusker Derek D  

Molecular biology of the cell 20150506 13


The coupling of endocytosis and exocytosis underlies fundamental biological processes ranging from fertilization to neuronal activity and cellular polarity. However, the mechanisms governing the spatial organization of endocytosis and exocytosis require clarification. Using a quantitative imaging-based screen in budding yeast, we identified 89 mutants displaying defects in the localization of either one or both pathways. High-resolution single-vesicle tracking revealed that the endocytic and exo  ...[more]

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