Identification of a yeast transcription factor IID subunit, TSG2/TAF48.

J Biol Chem

Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.

Published: June 2000

AI Article Synopsis

  • TFIID is a complex essential for transcription that includes the TATA-binding protein (TBP) and TAFs, and the study focuses on the role of TAF(II)68/61p in this process.
  • The C-terminal alpha-helix of TAF(II)68/61p is crucial for its interaction with TBP, stability of the TFIID complex, and proper gene transcription in yeast.
  • The study identifies TSG2 as a high copy suppressor of the TAF68/61 mutation, which interacts with TAF(II)68/61p and is vital for TFIID stability and transcription of numerous yeast genes.

Article Abstract

The RNA polymerase II general transcription factor TFIID is a complex containing the TATA-binding protein (TBP) and associated factors (TAFs). We have used a mutant allele of the gene encoding yeast TAF(II)68/61p to analyze its function in vivo. We provide biochemical and genetic evidence that the C-terminal alpha-helix of TAF(II)68/61p is required for its direct interaction with TBP, the stable incorporation of TBP into the TFIID complex, the integrity of the TFIID complex, and the transcription of most genes in vivo. This is the first evidence that a yeast TAF(II) other than TAF(II)145/130 interacts with TBP, and the implications of this on the interpretation of data obtained studying TAF(II) mutants in vivo are discussed. We have identified a high copy suppressor of the TAF68/61 mutation, TSG2, that has sequence similarity to a region of the SAGA subunit Ada1. We demonstrate that it directly interacts with TAF(II)68/61p in vitro, is a component of TFIID, is required for the stability of the complex in vivo, and is necessary for the transcription of many yeast genes. On the basis of these functions, we propose that Tsg2/TAF(II)48p is the histone 2A-like dimerization partner for the histone 2B-like TAF(II)68/61p in the yeast TFIID complex.

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http://dx.doi.org/10.1074/jbc.M001635200DOI Listing

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