Core-sigma interaction: Probing the interaction of the bacteriophage T4 gene 55 promoter recognition protein with E. coli RNA polymerase core

• Published in: The EMBO journal 1998-03, Vol.17 (5), p.1467-1475
• Main Authors: Leonetti, J-P, Wong, K, Geiduschek, E P
• Format: Article
• Language: English
• ISSN: 0261-4189
• DOI: 10.1093/emboj/17.5.1467

The bacterial RNA polymerase sigma subunits are key participants in the early steps of RNA synthesis, conferring specificity of promoter recognition, facilitating promoter opening and promoter clearance, and responding to diverse transcriptional regulators. The T4 gene 55 protein (gp55), the sigma protein of the bacteriophage T4 late genes, is one of the smallest and most divergent members of this family. Protein footprinting was used to identify segments of gp55 that become buried upon binding to RNA polymerase core, and are therefore likely to constitute its interface with the core enzyme. Site-directed mutagenesis in two parts of this contact surface generated gene 55 proteins that are defective in polymerase-binding to different degrees. Alignment with the sequences of the sigma proteins and with a recently determined structure of a large segment of sigma super(70) suggests that the gp55 counterpart of sigma super(70) regions 2.1 and 2.2 is involved in RNA polymerase core binding, and that sigma super(70) and gp55 may be structurally similar in this region. The diverse phenotypes of the mutants implicate this region of gp55 in multiple aspects of sigma function.