Umeå University's logo

umu.sePublications
System disruptions
There are recurring service disruptions on some of the search portals due to high traffic. We are working to resolve the issue, you may temporarily encounter an error message.
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
The Med1 subunit of the yeast mediator complex is involved in both transcriptional activation and repression
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics. Department of Medical Biochemistry and Microbiology, Uppsala University Biomedical Center, Uppsala, Sweden.
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics. Department of Medical Biochemistry and Microbiology, Uppsala University Biomedical Center, Uppsala, Sweden.
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics. Department of Medical Biochemistry and Microbiology, Uppsala University Biomedical Center, Uppsala, Sweden.
1999 (English)In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 96, no 2, p. 376-381Article in journal (Refereed) Published
Abstract [en]

The mediator complex is essential for regulated transcription in vitro. In the yeast Saccharomyces cerevisiae, mediator comprises >15 subunits and interacts with the C-terminal domain of the largest subunit of RNA polymerase II, thus forming an RNA polymerase II holoenzyme. Here we describe the molecular cloning of the MED1 cDNA encoding the 70-kDa subunit of the mediator complex. Yeast cells lacking the MED1 gene are viable but show a complex phenotype including partial defects in both repression and induction of the GAL genes. Together with results on other mediator subunits, this implies that the mediator is involved in both transcriptional activation and repression. Similar to mutations in the SRB10 and SRB11 genes encoding cyclin C and the cyclin C-dependent kinase, a disruption of the MED1 gene can partially suppress loss of the Snf1 protein kinase. We further found that a lexA-Med1 fusion protein is a strong activator in srb11 cells, which suggests a functional link between Med1 and the Srb10/11 complex. Finally, we show that the Med2 protein is lost from the mediator on purification from Med1-deficient cells, indicating a physical interaction between Med1 and Med2.

Place, publisher, year, edition, pages
Proceedings of the National Academy of Sciences (PNAS), 1999. Vol. 96, no 2, p. 376-381
National Category
Molecular Biology
Identifiers
URN: urn:nbn:se:umu:diva-236220DOI: 10.1073/pnas.96.2.376PubMedID: 9892641Scopus ID: 2-s2.0-0033582218OAI: oai:DiVA.org:umu-236220DiVA, id: diva2:1943020
Available from: 2025-03-07 Created: 2025-03-07 Last updated: 2025-03-10Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Björklund, Stefan

Search in DiVA

By author/editor
Björklund, Stefan
By organisation
Department of Medical Biochemistry and Biophysics
In the same journal
Proceedings of the National Academy of Sciences of the United States of America
Molecular Biology

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 179 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf