Projects per year
Abstract
The Escherichia coli melR gene encodes the MelR transcription factor that controls melibiose utilization. Expression of melR is autoregulated by MelR, which represses the melR promoter by binding to a target that overlaps the transcript start. Here, we show that MelR-dependent repression of the melR promoter can be enhanced by the presence of a second single DNA site for MelR located up to 250 base pairs upstream. Parallels with AraC-dependent repression at the araC-araBAD regulatory region and the possibility of the MelR-dependent repression loop formation are discussed. The results show that MelR bound at two distal loci can cooperate together in transcriptional repression.
Original language | English |
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Pages (from-to) | 62-7 |
Number of pages | 6 |
Journal | FEMS Microbiology Letters |
Volume | 338 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2013 |
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Dive into the research topics of 'Two DNA sites for MelR in the same orientation are sufficient for optimal MelR-dependent repression at the Escherichia coli melR promoter'. Together they form a unique fingerprint.Projects
- 1 Finished
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Molecular Mechanism of Triggering of a Bacterial Transcription Activator
Biotechnology & Biological Sciences Research Council
1/12/04 → 14/09/08
Project: Research Councils