Cell division genes ftsQAZ in escherichia coli require distant cis- acting signals upstream of ddlB for full expression
A transcriptional reporter fusion has been introduced into the chromosomal ftsZ locus in such a way that all transcription that normally reaches ftsZ can be monitored. The new Φ(ftsZ-lacZ) fusion yields four times more β-galactosidase activity than a ddlB-ftsQAZ-lacZ fusion on a lambda prophage vector. A strongly polar ddlB::Ω insertion prevents contributions from signals upstream of the ftsQAZ pr
