In bacterial transcription, diverse sigma-family promoter recognition prote
ins compete for a common RNA polymerase core. Bacteriophage T4 infection ul
timately reduces this competition to a duel between activated viral middle
and enhanced late transcription, involving two sigma proteins, two phage-en
coded activator proteins and two phage-specific co-activators. This competi
tion has been analyzed in vitro, and the relative abundances in T4-infected
Escherichia coli of the participating proteins have been measured. Activat
ed late transcription holds an advantage over activated middle transcriptio
n, especially at higher ionic strength. This advantage is further compounde
d by ADP-ribosylation of the RNA polymerase alpha subunits, and by the phag
e-specific, RNA polymerase core-bound RpbA subunit. The largest contributio
n to the middle-late competition is made by gp55, the late sigma factor, bu
t not enough of gp55 is produced during T4 infection to shut off middle tra
nscription by direct competition with sigma 70. AsiA, the originally identi
fied anti-sigma protein is not a major determinant of middle-late competiti
on. (C) 1999 Academic Press.