Abstract

The transcription factor USF1 belongs to the family of basic helix-loop-helix proteins that are involved in the regulation of various important cellular processes. Here we characterized the factors involved in the activation of transcription by upstream stimulatory factor 1 (USF1) in a reconstituted class II gene transcription system. Activation of transcription by both wild type USF1 and a GAL-USF (amino acids 1-94 of the yeast activator protein GAL4 fused to amino acids 17-196 of USF) fusion protein required the presence of at least one positive cofactor. A novel positive cofactor (PC5) that functions specifically through the activation domain of USF1 was partially purified and biochemicaly distinguished from previously described positive cofactors. The mechanism by which PC5 mediates activation of transcription through USF1 was investigated in order-of-addition experiments. PC5 had to be present during binding of transcription factor (TF) IID to the TATA box to observe transcriptional activation. However, this event alone did not result in transcriptional activation, which also required the presence of the activator and of PC5 after binding of TFIID. Hence, PC5 may enter transcription during binding of TFIID to function in concert with the activator during subsequent steps in transcription.

Highlights

  • Upstream stimulatory factor (USF)1 was originally described as an activity derived from HeLa nuclear extract that binds to an element (E-box) upstream of the adenovirus major late promoter [1,2,3]

  • These protein fractions (PC1 to PC4) were chromatographically separated, and the PCs were shown to be required and sufficient to facilitate activator-dependent transcription in a purified transcription system, which contained a complete set of GTFs, including a native TFIID complex consisting of TBP and TAFs [41]

  • In order-of-addition experiments we show that PC5 initiates stimulation of transcription during binding of TFIID to the promoter but completes its effects in conjunction with an activator after DA complex formation

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Summary

Introduction

Upstream stimulatory factor (USF) was originally described as an activity derived from HeLa nuclear extract that binds to an element (E-box) upstream of the adenovirus major late promoter [1,2,3]. Sequence analysis showed USF1 and USF2 to be members of the basic helix-loop-helix (bHLH)/leucin zipper family of transcription factors. In nuclear extracts recombinant USF1, indistinguishable from purified USF, activates transcription of the major late promoter [14]. Recombinant USF1 is able to activate transcription in nuclear extracts indistinguishable from natural USF [14, 15], activation potential in reconstituted transcription systems is substantially reduced during purification of natural USF [16]

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