Abstract:
:In bacterial transcription, diverse sigma-family promoter recognition proteins compete for a common RNA polymerase core. Bacteriophage T4 infection ultimately reduces this competition to a duel between activated viral middle and enhanced late transcription, involving two sigma proteins, two phage-encoded activator proteins and two phage-specific co-activators. This competition has been analyzed in vitro, and the relative abundances in T4-infected Escherichia coli of the participating proteins have been measured. Activated late transcription holds an advantage over activated middle transcription, especially at higher ionic strength. This advantage is further compounded by ADP-ribosylation of the RNA polymerase alpha subunits, and by the phage-specific, RNA polymerase core-bound RpbA subunit. The largest contribution to the middle-late competition is made by gp55, the late sigma factor, but not enough of gp55 is produced during T4 infection to shut off middle transcription by direct competition with sigma(70). AsiA, the originally identified anti-sigma protein is not a major determinant of middle-late competition.
journal_name
J Mol Bioljournal_title
Journal of molecular biologyauthors
Kolesky S,Ouhammouch M,Brody EN,Geiduschek EPdoi
10.1006/jmbi.1999.2953keywords:
subject
Has Abstractpub_date
1999-08-13 00:00:00pages
267-81issue
2eissn
0022-2836issn
1089-8638pii
S0022-2836(99)92953-4journal_volume
291pub_type
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