Preparation and topology of the Mediator middle module.

Nucleic Acids Res

Department of Biochemistry, Gene Center Munich and Center for Integrated Protein Science Munich, Ludwig-Maximilians-Universität München, Feodor-Lynen-St. 25, 81377 Munich, Germany.

Published: June 2010

AI Article Synopsis

  • Mediator is a crucial coactivator complex for RNA polymerase II transcription, made up of 25 subunits organized into distinct modules.
  • The study details protocols to isolate both pure endogenous and recombinant Mediator's middle module from yeast, which contains seven subunits that work together.
  • Advanced analysis techniques show that the middle module has a flexible, elongated structure, and specific subunits (Med7 and Med4) act as platforms for forming important subcomplexes in the Mediator's architecture.

Article Abstract

Mediator is the central coactivator complex required for regulated transcription by RNA polymerase (Pol) II. Mediator consists of 25 subunits arranged in the head, middle, tail and kinase modules. Structural and functional studies of Mediator are limited by the availability of protocols for the preparation of recombinant modules. Here, we describe protocols for obtaining pure endogenous and recombinant complete Mediator middle module from Saccharomyces cerevisiae that consists of seven subunits: Med1, 4, 7, 9, 10, 21 and 31. Native mass spectrometry reveals that all subunits are present in equimolar stoichiometry. Ion-mobility mass spectrometry, limited proteolysis, light scattering and small-angle X-ray scattering all indicate a high degree of intrinsic flexibility and an elongated shape of the middle module. Protein-protein interaction assays combined with previously published data suggest that the Med7 and Med4 subunits serve as a binding platform to form the three heterodimeric subcomplexes, Med7N/21, Med7C/31 and Med4/9. The subunits, Med1 and Med10, which bridge to the Mediator tail module, bind to both Med7 and Med4.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2879511PMC
http://dx.doi.org/10.1093/nar/gkq029DOI Listing

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