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Nucleic Acids Research, 1994, Vol. 22, No. 10 1855-1860
© 1994


MOLECULAR BIOLOGY

The ß recombinase from the Streptococcal plasmid pSM19035 represses its own transcription by holding the RNA polymerase at the promoter region

Fernando Rojo1,2 and Juan C. Alonso1,3,*

1Centro Nacional de Biotecnología, C.S.I.C., Campus Universidad Autónoma 28049 Madrid 2Centro de Biología Molecular ‘Severo Ochoa’, C.S.I.C., Universidad Autónoma Canto Blanco, 28049 Madrid, Spain 3Max-Planck-Institut für molekulare Genetik Ihnestrasse 73, D-14195 Berlin, Germany

*To whom correspondence should be addressed at: Centro Nacional de Biotecnología, C.S.I.C., Campus Universidad Autónoma, 28049 Madrid, Spain.

Received February 2, 1994. Revised April 12, 1994. Accepted April 12, 1994.

The ß protein encoded by the Streptococcus pyogenes plasmid pSM19035 is a site-specific recombinase involved in both resolution of plasmid multimers into monomers and DNA inversion. It has been proposed that the DNA region to which the ß recombinase binds to mediate recombination includes a promoter from which orf{alpha} and the ß gene are transcribed. We have determined the sites at which transcription of the orf{alpha} and the ß gene initiates in vitro and we have demonstrated that highly purified ß recombinase acts as a repressor of its own synthesis. The promoters are located within the ß recombinase binding site, which we have defined previously. The binding of the ß recombinase to its target site does not seem to exclude RNA polymerase from the promoter, despite the overlapping of their binding sites. Therefore, it is likely that the ß recombinase does not repress transcription by a mere steric hindrance on RNA polymerase binding.


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