MECHANISM OF MACROMOLECULAR EXPORT FROM THE NUCLEUS
Project Number7R01GM058065-02
Contact PI/Project LeaderWEIS, KARSTEN
Awardee OrganizationUNIVERSITY OF CALIFORNIA BERKELEY
Description
Abstract Text
DESCRIPTION (adapted from the applicant's abstract): Export of RNA and
protein from the nucleus into the cytoplasm is a fundamental cellular
process and a key step in the control of eukaryotic gene expression. The
mechanisms governing these transport events are still poorly understood
but kinetic competition studies in Xenopus oocytes have indicated that
different RNA classes, including mRNA, snRNA, tRNA and rRNA use distinct
export pathways. Since most, if not all RNAs, are associated with proteins
in the nucleus it was suggested that RNA export events are mediated by
proteins in the nucleus it was suggested that RNA export events are
mediated by proteins containing appropriate nuclear export signals (NESs).
This is supported by the identification of small transferable signals in
proteins that cause their rapid and active export from the nucleus. The
long-term goal of the proposed research is to characterize different RNA
and protein export pathways in the yeast S. cerevisiae and to understand
the nuclear export mechanisms at a molecular level. More specifically,
three specific aims are proposed: (1) The P.I. will characterize the
nuclear export factor export in 1 (Xpo1p/Crm1p) and its role in mRNA
export. A variety of biochemical and genetic approaches will be used to
identify factors which interact with Xpo1p. The role of the GTPase Ran in
regulating the interaction of Xpo1p with other cellular factors will be
examined and the adapter(s) that mediate(s) Xpo10,s role in mRNA export
will be characterized. (2) The NES-mediated nuclear protein export
machinery will be dissected. Genetic approaches will be explored to
identify additional components of the NES-protein export machinery. This
export pathway will be used as a model system to understand the molecular
details of how macromolecules are transported through the nuclear pore
complex into the cytoplasm. (3) Finally, the P.I. will determine whether
distinct RNA export pathways exist in yeast. In situ labeling in fixed and
live cells will be used to characterize the export of the different RNA
classes in several mutant backgrounds. If distinct pathways are
identified, factors that mediate and regulate these export events will be
identified.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
RNA binding proteinSaccharomyces cerevisiaebiological signal transductionfungal geneticsguanosinetriphosphatasesin situ hybridizationintracellular transportmessenger RNAmolecular cloningnuclear membranenucleic acid sequenceprotein structure functionprotein transportsite directed mutagenesistransport proteinsyeast two hybrid system
No Sub Projects information available for 7R01GM058065-02
Publications
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