Your browser doesn't support javascript.
loading
Cross-kingdom chemical communication drives a heritable, mutually beneficial prion-based transformation of metabolism.
Jarosz, Daniel F; Brown, Jessica C S; Walker, Gordon A; Datta, Manoshi S; Ung, W Lloyd; Lancaster, Alex K; Rotem, Assaf; Chang, Amelia; Newby, Gregory A; Weitz, David A; Bisson, Linda F; Lindquist, Susan.
Afiliação
  • Jarosz DF; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Departments of Chemical and Systems Biology and of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Brown JCS; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
  • Walker GA; Department of Viticulture and Enology, University of California, Davis, Davis, CA 95616, USA.
  • Datta MS; Computational and Systems Biology Initiative, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
  • Ung WL; Department of Physics, Harvard University, Cambridge, MA 02138, USA.
  • Lancaster AK; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA; Center for Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.
  • Rotem A; Department of Physics, Harvard University, Cambridge, MA 02138, USA.
  • Chang A; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
  • Newby GA; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
  • Weitz DA; Department of Physics, Harvard University, Cambridge, MA 02138, USA; School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
  • Bisson LF; Department of Viticulture and Enology, University of California, Davis, Davis, CA 95616, USA. Electronic address: lfbisson@ucdavis.edu.
  • Lindquist S; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA. Electronic address: lindquist_admin@wi.mit.edu.
Cell ; 158(5): 1083-1093, 2014 Aug 28.
Article em En | MEDLINE | ID: mdl-25171409
ABSTRACT
In experimental science, organisms are usually studied in isolation, but in the wild, they compete and cooperate in complex communities. We report a system for cross-kingdom communication by which bacteria heritably transform yeast metabolism. An ancient biological circuit blocks yeast from using other carbon sources in the presence of glucose. [GAR(+)], a protein-based epigenetic element, allows yeast to circumvent this "glucose repression" and use multiple carbon sources in the presence of glucose. Some bacteria secrete a chemical factor that induces [GAR(+)]. [GAR(+)] is advantageous to bacteria because yeast cells make less ethanol and is advantageous to yeast because their growth and long-term viability is improved in complex carbon sources. This cross-kingdom communication is broadly conserved, providing a compelling argument for its adaptive value. By heritably transforming growth and survival strategies in response to the selective pressures of life in a biological community, [GAR(+)] presents a unique example of Lamarckian inheritance.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Príons / Staphylococcus hominis / Epigênese Genética Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Príons / Staphylococcus hominis / Epigênese Genética Idioma: En Ano de publicação: 2014 Tipo de documento: Article