Continuing genetic and cytological investigations of the filamentous ascomycete Neurospora will concern chromosome rearrangements - their origin, behavior, and applications; segregation-distorting Spore killer mutants - their chromosomal basis, mode of action, and significance in nature; and chromosome behavior in meiosis, as revealed by the synaptonemal complex and recombination nodules of nuclei reconstructed from thin sections in crosses that involve chromosome rearrangements and meiotic mutants. Mutants affecting events in the ascus will be analyzed. A locus-specific mutator system will be investigated, and other example of instability will be examined. - Genetic analysis of natural populations will be continued, using 4000 strains previously collected from five continents, with special interest in meiotic drive, the genetic isolation mechanisms involved in speciation, and dysgenic consequences of crosses between unrelated strains. -Aims of the research are to develop Neurospora as a model organism for genetics, cytology, and molecular biology; to increase understanding of chromosome organization in a small eukaryote genome; to analyze recombination, meiosis, and other events in the developing ascus; and to extend population genetics to organisms having a predominantly haploid life cycle. Knowledge of Neurospora Segentel aneuploids that are generated in meiosis parallel chromosomal anomalies responsible for birth defects in man.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AI001462-39
Application #
2057719
Study Section
Special Emphasis Panel (NSS)
Project Start
1977-09-01
Project End
1996-10-31
Budget Start
1994-11-01
Budget End
1995-10-31
Support Year
39
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Stanford University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305