| Literature DB >> 1719220 |
B Ghosh1, E Grzadzielska, P Bhattacharya, E Peralta, J DeVito, A Das.
Abstract
Transcription of the ribosomal RNA operons (rrn) in Escherichia coli is subject to an antitermination mechanism whereby RNA polymerase is modified to a termination-resistant form during transit through the rrn leader region. This antitermination mechanism is unable to overcome the T1-T2 terminator cluster located at the end of an rrn operon, such as rrnB. We have tested the specificity with which the T1-T2 terminators override an antitermination mechanism, by placing the terminator cluster downstream from the nut and qut sites recognized by phage lambda N and Q gene antiterminators, respectively. Measurement of downstream gene expression shows that RNA polymerase modified by either N or Q reads through the T1-T2 terminators quite efficiently. This supports the view that T1-T2 are not superterminators, and that the rrn antitermination mechanism may have a restricted terminator specificity.Entities:
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Year: 1991 PMID: 1719220 DOI: 10.1016/0022-2836(91)90737-q
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469