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Targeted in Situ Mutagenesis of Histone Genes in Budding Yeast
Published on: January 26, 2017
Human DNA methyltransferase gene-transformed yeasts display an inducible flocculation inhibited by
Kei-Ichi Sugiyama1, Makiko Takamune1, Hiroko Furusawa1
1Division of Genetics and Mutagenesis, National Institute of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan.
Abstract:
Mammalian DNA methyltransferases (DNMTs) play an important role in establishing and maintaining the proper regulation of epigenetic information. However, it remains unclear whether mammalian DNMTs can be functionally expressed in yeasts, which probably lack endogenous DNMTs. We cotransformed the budding yeast Saccharomyces cerevisiae with the human DNMT1 gene, which encodes a methylation maintenance enzyme, and the DNMT3A/3B genes, which encode de novo methylation enzymes, in an expression vector also containing the GAL1 promoter, which is induced by galactose, and examined the effects of the DNMT inhibitor 5-aza-2'-deoxycytidine (5AZ) on cell growth. Transformed yeast strains grown in galactose- and glucose-containing media showed growth inhibition, and their growth rate was unaffected by 5AZ. Conversely, 5AZ, but not 2'-deoxycytidine, dose-dependently interfered with the flocculation exhibited by DNMT-gene transformants grown in glucose-containing medium. Further investigation of the properties of this flocculation indicated that it may be dependent on the expression of a Flocculin-encoding gene, FLO1. Taken together, these findings suggest that DNMT-gene transformed yeast strains functionally express these enzymes and represent a useful tool for in vivo screening for DNMT inhibitors.
Insights
Mammalian DNA methyltransferases (DNMTs) functionally expressed in yeast. These DNMT-transformed yeast strains show potential for screening novel DNMT inhibitors by affecting flocculation.
Area of Science:
- Epigenetics
- Molecular Biology
- Yeast Genetics
Background:
- Mammalian DNA methyltransferases (DNMTs) are crucial for epigenetic regulation.
- The functional expression of mammalian DNMTs in yeast, which lack endogenous DNMTs, is not well understood.
Purpose of the Study:
- To investigate the functional expression of human DNMT1, DNMT3A, and DNMT3B genes in Saccharomyces cerevisiae.
- To evaluate the utility of DNMT-transformed yeast strains for screening DNMT inhibitors.
Main Methods:
- Cotransformation of yeast with human DNMT genes under a galactose-inducible promoter (GAL1).
- Assessment of cell growth and flocculation in response to the DNMT inhibitor 5-aza-2'-deoxycytidine (5AZ).
Main Results:
- Transformed yeast strains exhibited growth inhibition in galactose- and glucose-containing media, independent of 5AZ.
- 5AZ dose-dependently interfered with yeast flocculation, suggesting DNMT activity influenced FLO1 gene expression.
- 2'-deoxycytidine did not affect flocculation.
Conclusions:
- Human DNMT genes are functionally expressed in yeast.
- DNMT-transformed yeast strains provide a viable system for in vivo screening of DNMT inhibitors.

