The long-term objective of the research proposed is to develop understanding of growth polarity in eukaryotic organisms through the elucidation of the molecular mechanisms of hyphal growth in the filamentous fungus Neurospora crassa. A class of ten N. crassa ropy mutants has been identified that are defective in normal hyphal growth. One of the genes, ro-1, encodes the heavy chain of cytoplasmic dynein, a microtubule-dependent motor that is required for retrograde transport of vesicles in axons of nerve cells. It is proposed that the remaining phenotypically identical ro mutants identify genes that code for additional subunits or regulators of N. crassa cytoplasmic dynein. The specific objective of this study is to genetically dissect N. crassa cytoplasmic dynein and determine its role in vesicle transport and hyphal growth. The experimental approaches are: (1) molecular analysis of ro-1, the gene encoding cytoplasmic dynein heavy chain; and (2) genetic identification of all ro complementation groups and isolation and characterization of ro genes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21GM051217-02
Application #
2189589
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1994-09-01
Project End
1996-08-31
Budget Start
1995-09-01
Budget End
1996-08-31
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Texas A&M University
Department
Biology
Type
Schools of Earth Sciences/Natur
DUNS #
City
College Station
State
TX
Country
United States
Zip Code
77845