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Redundant roles for the TFIID and SAGA complexes in global transcription

Author

Listed:
  • Tong Ihn Lee

    (Whitehead Institute for Biomedical Research, Nine Cambridge Center
    Massachusetts Institute of Technology)

  • Helen C. Causton

    (Whitehead Institute for Biomedical Research, Nine Cambridge Center)

  • Frank C. P. Holstege

    (Whitehead Institute for Biomedical Research, Nine Cambridge Center
    Department for Medical Genetics University Medical Centre Utrecht)

  • Wu-Cheng Shen

    (Howard Hughes Medical Institute Program in Molecular Medicine, University of Massachusetts Medical Center)

  • Nancy Hannett

    (Whitehead Institute for Biomedical Research, Nine Cambridge Center)

  • Ezra G. Jennings

    (Whitehead Institute for Biomedical Research, Nine Cambridge Center
    Massachusetts Institute of Technology)

  • Fred Winston

    (Harvard Medical School)

  • Michael R. Green

    (Howard Hughes Medical Institute Program in Molecular Medicine, University of Massachusetts Medical Center)

  • Richard A. Young

    (Whitehead Institute for Biomedical Research, Nine Cambridge Center
    Massachusetts Institute of Technology)

Abstract

The transcription factors TFIID and SAGA are multi-subunit complexes involved in transcription by RNA polymerase II1,2. TFIID and SAGA contain common TATA-binding protein (TBP)-associated factor (TAFII) subunits and each complex contains a subunit with histone acetyltransferase activity3. These observations have raised questions about whether the functions of the two complexes in vivo are unique or overlapping. Here we use genome-wide expression analysis to investigate how expression of the yeast genome depends on both shared and unique subunits of these two complexes. We find that expression of most genes requires one or more of the common TAFII subunits, indicating that the functions of TFIID and SAGA are widely required for gene expression. Among the subunits shared by TFIID and SAGA are three histone-like TAFIIs, which have been proposed to form a sub-complex and mediate a common function in global transcription. Unexpectedly, we find that the histone-like TAFIIs have distinct roles in expression of the yeast genome. Most importantly, we show that the histone acetylase components of TFIID and SAGA (TAFII145 and Gcn5) are functionally redundant, indicating that expression of a large fraction of yeast genes can be regulated through the action of either complex.

Suggested Citation

  • Tong Ihn Lee & Helen C. Causton & Frank C. P. Holstege & Wu-Cheng Shen & Nancy Hannett & Ezra G. Jennings & Fred Winston & Michael R. Green & Richard A. Young, 2000. "Redundant roles for the TFIID and SAGA complexes in global transcription," Nature, Nature, vol. 405(6787), pages 701-704, June.
  • Handle: RePEc:nat:nature:v:405:y:2000:i:6787:d:10.1038_35015104
    DOI: 10.1038/35015104
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    Cited by:

    1. Helka Göös & Matias Kinnunen & Kari Salokas & Zenglai Tan & Xiaonan Liu & Leena Yadav & Qin Zhang & Gong-Hong Wei & Markku Varjosalo, 2022. "Human transcription factor protein interaction networks," Nature Communications, Nature, vol. 13(1), pages 1-16, December.

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