Abstract

Human U6 small nuclear RNA (snRNA) gene transcription by RNA polymerase III requires cooperative promoter binding involving the snRNA-activating protein complex (SNAP(c)) and the TATA-box binding protein (TBP). To investigate the role of SNAP(c) for TBP function at U6 promoters, TBP recruitment assays were performed using full-length TBP and a mini-SNAP(c) containing SNAP43, SNAP50, and a truncated SNAP190. Mini-SNAP(c) efficiently recruits TBP to the U6 TATA box, and two SNAP(c) subunits, SNAP43 and SNAP190, directly interact with the TBP DNA binding domain. Truncated SNAP190 containing only the Myb DNA binding domain is sufficient for TBP recruitment to the TATA box. Therefore, the SNAP190 Myb domain functions both to specifically recognize the proximal sequence element present in the core promoters of human snRNA genes and to stimulate TBP recognition of the neighboring TATA box present in human U6 snRNA promoters. The SNAP190 Myb domain also stimulates complex assembly with TBP and Brf2, a subunit of a snRNA-specific TFIIIB complex. Thus, interactions between the DNA binding domains of SNAP190 and TBP at juxtaposed promoter elements define the assembly of a RNA polymerase III-specific preinitiation complex.

Highlights

  • Transcription in eukaryotic organisms occurs by three different RNA polymerases that transcribe different classes of genes

  • To understand how TATA-box binding protein (TBP) is recruited to human U6 small nuclear RNA (snRNA) gene promoters, we have examined those proteins within snRNA-activating protein complex (SNAPc) which are important for interactions with TBP and for cooperative DNA binding of the U6 promoters by both SNAPc and TBP

  • A baculovirus-expressed mini-SNAPc with only three proteins, SNAP43, SNAP50, and SNAP190 containing amino acids 1–514 is sufficient for recruiting TBP to a U6 snRNA TATA box [43]

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Summary

Introduction

Transcription in eukaryotic organisms occurs by three different RNA polymerases that transcribe different classes of genes. Further analysis of SNAP43 and SNAP190 indicate that the SNAP190 Myb DNA binding domain plays a pivotal role in TBP recruitment and stimulates assembly of a complex containing TBP and the TFIIIB factor Brf2.

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