| dc.contributor.author | Jarosz, Daniel F. | |
| dc.contributor.author | Lancaster, Alex K. | |
| dc.contributor.author | Brown, Jessica Conrad | |
| dc.contributor.author | Lindquist, Susan | |
| dc.date.accessioned | 2016-12-05T20:16:45Z | |
| dc.date.available | 2016-12-05T20:16:45Z | |
| dc.date.issued | 2014-08 | |
| dc.identifier.issn | 00928674 | |
| dc.identifier.issn | 1097-4172 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/105721 | |
| dc.description.abstract | [GAR[superscript +]] is a protein-based element of inheritance that allows yeast (Saccharomyces cerevisiae) to circumvent a normal hallmark of their biology: extreme metabolic specialization for glucose fermentation. When glucose is present, even in trace quantities, yeast will not use other carbon
sources. [GAR[superscript +]] allows cells to circumvent this “glucose repression.” [GAR[superscript +]] is induced in yeast by a factor secreted by bacteria inhabiting their environment. We report that the de novo rates of [GAR[superscript +]] appearance correlate with the yeast’s ecological niche. Evolutionarily distant fungi possess similar epigenetic elements that are also induced by bacteria. As expected for a mechanism whose adaptive value originates from the selective pressures of life in biological communities, the ability of bacteria to induce [GAR[superscript +]] and the ability of yeast to respond to bacterial signals have been extinguished repeatedly during the extended monoculture of domestication. Thus, [GAR[superscript +]] is a broadly conserved adaptive strategy that links environmental and social cues to heritable changes in metabolism. | en_US |
| dc.description.sponsorship | G. Harold and Leila Y. Mathers Foundation | en_US |
| dc.description.sponsorship | Howard Hughes Medical Institute | en_US |
| dc.language.iso | en_US | |
| dc.publisher | Elsevier | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1016/j.cell.2014.07.024 | en_US |
| dc.rights | Creative Commons Attribution-NonCommercial-NoDerivs License | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | en_US |
| dc.source | PMC | en_US |
| dc.title | An Evolutionarily Conserved Prion-like Element Converts Wild Fungi from Metabolic Specialists to Generalists | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Jarosz, Daniel F. et al. “An Evolutionarily Conserved Prion-like Element Converts Wild Fungi from Metabolic Specialists to Generalists.” Cell 158.5 (2014): 1072–1082. | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
| dc.contributor.department | Whitehead Institute for Biomedical Research | en_US |
| dc.contributor.mitauthor | Brown, Jessica Conrad | |
| dc.contributor.mitauthor | Lindquist, Susan | |
| dc.relation.journal | Cell | en_US |
| dc.eprint.version | Author's final manuscript | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dspace.orderedauthors | Jarosz, Daniel F.; Lancaster, Alex K.; Brown, Jessica C.S.; Lindquist, Susan | en_US |
| dspace.embargo.terms | N | en_US |
| dc.identifier.orcid | https://orcid.org/0000-0003-1307-882X | |
| mit.license | PUBLISHER_CC | en_US |