DNA molecules exchange parts with each other in a variety of circumstances. In meiosis eukaryotic chromosomes break and join parts with strict adherance to homology, so that the order of gene loci is preserved. This process, generalized genetic recombination, will be investigated in the eukaryote Saccharomyces cerevisiae and in the bacteriophage Lambda. A fuller understanding of recombination may have implications for developmental anomalies, immune deficiencies, and cancer induction. The proposed invesitagations will seek and characterize nucleotide sequences that play special roles in recombination. These studies will include tests of hypotheses regarding the mechanism of action of the Chi sequence (5 feet GCTGGTGG). Recombination can be initiated by doulbe stand breaks in DNA. It is possible that such breaks are the normal mode of initiation in meiosis. That hypothesis will be tested as will hypotheses regarding the involvement of double stand breaks in prokaryotic recombination. In addition, improvements in gene cloning methodology will be attempted. The improved methods sought are in vitro packaging of Lambda DNA and in the cloning of DNA palindromes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033677-03
Application #
3283569
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1984-08-01
Project End
1987-07-31
Budget Start
1986-08-01
Budget End
1987-07-31
Support Year
3
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Oregon
Department
Type
Organized Research Units
DUNS #
948117312
City
Eugene
State
OR
Country
United States
Zip Code
97403
Tarkowski, Trudee A; Mooney, Duane; Thomason, Lynn C et al. (2002) Gene products encoded in the ninR region of phage lambda participate in Red-mediated recombination. Genes Cells 7:351-63
Copenhaver, G P; Housworth, E A; Stahl, F W (2002) Crossover interference in Arabidopsis. Genetics 160:1631-9
Stahl, F; Bowers Jr, R; Mooney, D et al. (2001) Growth and recombination of phage lambda in the presence of exonuclease V from Bacillus subtilis. Mol Gen Genet 264:716-23
Stahl, F W; Hillers, K J (2000) Heteroduplex rejection in yeast? Genetics 154:1913-6
Thompson, D A; Stahl, F W (1999) Genetic control of recombination partner preference in yeast meiosis. Isolation and characterization of mutants elevated for meiotic unequal sister-chromatid recombination. Genetics 153:621-41
Foss, H M; Hillers, K J; Stahl, F W (1999) The conversion gradient at HIS4 of Saccharomyces cerevisiae. II. A role for mismatch repair directed by biased resolution of the recombinational intermediate. Genetics 153:573-83
Hillers, K J; Stahl, F W (1999) The conversion gradient at HIS4 of Saccharomyces cerevisiae. I. Heteroduplex rejection and restoration of Mendelian segregation. Genetics 153:555-72
Stahl, F W (1998) Recombination in phage lambda: one geneticist's historical perspective. Gene 223:95-102
Zhou, H; Dahlquist, F W (1997) Phosphotransfer site of the chemotaxis-specific protein kinase CheA as revealed by NMR. Biochemistry 36:699-710
Stahl, M M; Thomason, L; Poteete, A R et al. (1997) Annealing vs. invasion in phage lambda recombination. Genetics 147:961-77

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