A eukaryotic cell is compartmentalized into numerous membrane-enclosed organelles. Of fundamental interest to cell biologists are the mechanisms by which these organelles achieve unique compositions. The goal of this proposal is an understanding of the selective transport of macromolecules into the nucleus. Such transport occurs through nuclear pores, which perforate the nuclear envelope and comprise the sites at which selective entry is controlled. Two approaches are proposed to address the mechanism of transport through the pores: 1) analysis of a particular pore protein, a 63 kd glycoprotein, and 2) analysis of the requirements for nuclear transport itself. Using a system which allows the rapid in vitro assay of nuclear transport, we have identified a nuclear pore protein required for pore function. A molecular and functional analysis of this protein is porposed. The protein will be purified and antibodies raised against it. With these tools, fundamental questions of pore function will be asked, including how the protein is involved, the role of the carbohydrate moiety of the protein in function, and whether this protein is integral to the structure of the nucleus. In a second approach to understanding nuclear transport, experiments are proposed to determine the minimal cellular components involved in transport. It should be possible to determine whether a carrier protein is required for nuclear transport, as it is for import into other organelles. Lastly, the role of ATP in either the recognition step or the translocation step of nuclear transport will be addressed.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033279-05
Application #
3282769
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1984-04-01
Project End
1992-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
5
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Type
Schools of Arts and Sciences
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Tam, Arvin B; Roberts, Lindsay S; Chandra, Vivek et al. (2018) The UPR Activator ATF6 Responds to Proteotoxic and Lipotoxic Stress by Distinct Mechanisms. Dev Cell 46:327-343.e7
Forbes, Douglass J; Travesa, Anna; Nord, Matthew S et al. (2015) Nuclear transport factors: global regulation of mitosis. Curr Opin Cell Biol 35:78-90
Schwartz, Michal; Travesa, Anna; Martell, Steven W et al. (2015) Analysis of the initiation of nuclear pore assembly by ectopically targeting nucleoporins to chromatin. Nucleus 6:40-54
Torres-Machorro, Ana Lilia; Clark, Lauren G; Chang, Christie S et al. (2015) The Set3 Complex Antagonizes the MYST Acetyltransferase Esa1 in the DNA Damage Response. Mol Cell Biol 35:3714-25
Basnet, Harihar; Su, Xue B; Tan, Yuliang et al. (2014) Tyrosine phosphorylation of histone H2A by CK2 regulates transcriptional elongation. Nature 516:267-71
Eustice, Moriah; Pillus, Lorraine (2014) Unexpected function of the glucanosyltransferase Gas1 in the DNA damage response linked to histone H3 acetyltransferases in Saccharomyces cerevisiae. Genetics 196:1029-39
Bernis, Cyril; Forbes, Douglass J (2014) Analysis of nuclear reconstitution, nuclear envelope assembly, and nuclear pore assembly using Xenopus in vitro assays. Methods Cell Biol 122:165-91
Bernis, Cyril; Swift-Taylor, Beth; Nord, Matthew et al. (2014) Transportin acts to regulate mitotic assembly events by target binding rather than Ran sequestration. Mol Biol Cell 25:992-1009
Powers, Maureen A; Forbes, Douglass J (2012) Nuclear transport: beginning to gel? Curr Biol 22:R1006-9
Fichtman, Boris; Ramos, Corinne; Rasala, Beth et al. (2010) Inner/Outer nuclear membrane fusion in nuclear pore assembly: biochemical demonstration and molecular analysis. Mol Biol Cell 21:4197-211

Showing the most recent 10 out of 45 publications