A common bacterial metabolite elicits prion-based bypass of glucose repression.
David M GarciaDavid DietrichJon ClardyDaniel F JaroszPublished in: eLife (2016)
Robust preference for fermentative glucose metabolism has motivated domestication of the budding yeast Saccharomyces cerevisiae. This program can be circumvented by a protein-based genetic element, the [GAR+] prion, permitting simultaneous metabolism of glucose and other carbon sources. Diverse bacteria can elicit yeast cells to acquire [GAR+], although the molecular details of this interaction remain unknown. Here we identify the common bacterial metabolite lactic acid as a strong [GAR+] inducer. Transient exposure to lactic acid caused yeast cells to heritably circumvent glucose repression. This trait had the defining genetic properties of [GAR+], and did not require utilization of lactic acid as a carbon source. Lactic acid also induced [GAR+]-like epigenetic states in fungi that diverged from S. cerevisiae ~200 million years ago, and in which glucose repression evolved independently. To our knowledge, this is the first study to uncover a bacterial metabolite with the capacity to potently induce a prion.
Keyphrases
- lactic acid
- saccharomyces cerevisiae
- induced apoptosis
- blood glucose
- cell cycle arrest
- genome wide
- endoplasmic reticulum stress
- oxidative stress
- signaling pathway
- metabolic syndrome
- quality improvement
- cell wall
- drinking water
- high glucose
- adipose tissue
- type diabetes
- diabetic rats
- endothelial cells
- cell proliferation
- protein protein
- brain injury
- weight loss
- cerebral ischemia