The object of the research described in this proposal is to expand our knowledge of development in general and of meiosis in particular, using as a model system the meiotic life cycle of the yeast Saccharomyces cerevisiae. We intend to use a set of Gamma-Charon 28 yeast chimeric bacteriophage, each of which contains a gene which is transcribed in meiotic cells but either much less or not at all in mitotic cells, to explore the mechanism of regulation of gene expression during development. In order to do this we will distinguish those genes which are required for sporulation (sporulation-essential) from the sporulation-specific ones by using transformation to disrupt the chromosomal copy and then determining the phenotype of the homozygous mutant cells. We already know that the transcripts from several of these genes appear in the cells at about meiosis I. We will determine the time and rate of synthesis and breakdown of the transcripts from these genes, and we will determine when they appear on polysomes, in order to ascertain whether post-transcriptional regulation occurs. We will construct fusions of these genes with the E. coli lac Z gene, determine whether regulation of the fused gene is normal, and then use the fusion products to select for mutations, both cis and trans acting, which affect regulation. All mutants isolated will be subjected to standard genetic analysis. We expect from this work to learn about the molecular basis of the regulation of gene expression during development; in particular, we hope to begin to understand the way in which temporal cycles are controlled. This knowledge will help us to approach rationally problems in birth defects, neoplasia, and immunoonotology, as well as contributing to our understanding of basic biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033305-02
Application #
3282855
Study Section
Genetics Study Section (GEN)
Project Start
1984-05-01
Project End
1987-04-30
Budget Start
1985-05-01
Budget End
1986-04-30
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Michigan State University
Department
Type
Schools of Arts and Sciences
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Muthukumar, G; Suhng, S H; Magee, P T et al. (1993) The Saccharomyces cerevisiae SPR1 gene encodes a sporulation-specific exo-1,3-beta-glucanase which contributes to ascospore thermoresistance. J Bacteriol 175:386-94
Pugh, T A; Shah, J C; Magee, P T et al. (1989) Characterization and localization of the sporulation glucoamylase of Saccharomyces cerevisiae. Biochim Biophys Acta 994:200-9
Smith, L M; Robbins, L G; Kennedy, A et al. (1988) Identification and characterization of mutations affecting sporulation in Saccharomyces cerevisiae. Genetics 120:899-907