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J Biol Chem, Vol. 274, Issue 16, 10743-10750, April 16, 1999
,
From the Golgi membranes and Golgi-derived vesicles are
associated with multiple cytoskeletal proteins and motors, the
diversity and distribution of which have not yet been defined. Carrier
vesicles were separated from Golgi membranes, using an in
vitro budding assay, and different populations of vesicles were
separated using sucrose density gradients. Three main populations of
vesicles labeled with Centre for Molecular and Cellular Biology,
-COP, 
-adaptin, or p200/myosin II were
separated and analyzed for the presence of actin/actin-binding
proteins. -Actin was bound to Golgi cisternae and to all populations
of newly budded vesicles. Centractin was selectively associated with vesicles co-distributing with -COP-vesicles, while p200/myosin II
(non-muscle myosin IIA) and non-muscle myosin IIB were found on
different vesicle populations. Isoforms of the Tm5 tropomyosins were
found on selected Golgi-derived vesicles, while other Tm isoforms did
not colocalize with Tm5 indicating the association of specialized actin
filaments with Golgi-derived vesicles. Golgi-derived vesicles were
shown to bind to F-actin polymerized from cytosol with Jasplakinolide.
Thus, newly budded, coated vesicles derived from Golgi membranes can
bind to actin and are customized for differential interactions with
microfilaments by the presence of selective arrays of actin-binding proteins.
Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.
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