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This study investigates the functional conservation of the MET17 gene in methionine biosynthesis by comparing the S. cerevisiae MET17 and S. pombe Met17 homologs. Using various molecular techniques, the research demonstrated that both genes could complement methionine biosynthesis mutations in S. cerevisiae, with S. cerevisiae MET17 showing more robust functionality. The findings emphasize the utility of GAL1-regulated plasmid systems for analyzing gene function and expression in yeast models.

Author

izhusti

Language

EN