A common bacterial metabolite elicits prion-based bypass of glucose repression

Author:

Garcia David M1ORCID,Dietrich David2ORCID,Clardy Jon2ORCID,Jarosz Daniel F13ORCID

Affiliation:

1. Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, United States

2. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, United States

3. Department of Developmental Biology, Stanford University School of Medicine, Stanford, United States

Abstract

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.

Funder

National Institutes of Health

National Science Foundation

Searle Scholars Program

Ford Foundation

Burroughs Wellcome Fund

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference56 articles.

1. Comprehensive review on lactate metabolism in human health;Adeva-Andany;Mitochondrion,2014

2. A bacterial sulfonolipid triggers multicellular development in the closest living relatives of animals;Alegado;eLife,2012

3. Glucosamine resistance in yeast. I. A preliminary genetic analysis;Ball;Genetics,1976

4. Saccharomyces cerevisiae forms D-2-Hydroxyglutarate and couples its degradation to D-Lactate formation via a cytosolic transhydrogenase;Becker-Kettern;Journal of Biological Chemistry,2016

Cited by 41 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3