Volume 54, Issue 1 pp. 198-211
Free Access

RNase HI overproduction is required for efficient full-length RNA synthesis in the absence of topoisomerase I in Escherichia coli

Imad Baaklini

Imad Baaklini

Département de microbiologie et immunologie, Université de Montréal, C.P. 6128, Succ. Centre-ville, Montréal, P. Québec, Canada, H3C 3J7.

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Chadi Hraiky

Chadi Hraiky

Département de microbiologie et immunologie, Université de Montréal, C.P. 6128, Succ. Centre-ville, Montréal, P. Québec, Canada, H3C 3J7.

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Fabien Rallu

Fabien Rallu

Département de microbiologie et immunologie, Université de Montréal, C.P. 6128, Succ. Centre-ville, Montréal, P. Québec, Canada, H3C 3J7.

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Yuk-Ching Tse-Dinh

Yuk-Ching Tse-Dinh

Department of Biochemistry and Molecular Biology, New York Medical College, Valhalla, NY 10595, USA.

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Marc Drolet

Corresponding Author

Marc Drolet

Département de microbiologie et immunologie, Université de Montréal, C.P. 6128, Succ. Centre-ville, Montréal, P. Québec, Canada, H3C 3J7.

E-mail [email protected]; Tel. (+1) 514 343 5796; Fax (+1) 514 343 5701.Search for more papers by this author
First published: 03 August 2004
Citations: 63

Summary

It has long been known that Escherichia coli cells deprived of topoisomerase I (topA null mutants) do not grow. Because mutations reducing DNA gyrase activity and, as a consequence, negative supercoiling, occur to compensate for the loss of topA function, it has been assumed that excessive negative supercoiling is somehow involved in the growth inhibition of topA null mutants. However, how excess negative supercoiling inhibits growth is still unknown. We have previously shown that the overproduction of RNase HI, an enzyme that degrades the RNA portion of an R-loop, can partially compensate for the growth defects because of the absence of topoisomerase I. In this article, we have studied the effects of gyrase reactivation on the physiology of actively growing topA null cells. We found that growth immediately and almost completely ceases upon gyrase reactivation, unless RNase HI is overproduced. Northern blot analysis shows that the cells have a significantly reduced ability to accumulate full-length mRNAs when RNase HI is not overproduced. Interestingly, similar phenotypes, although less severe, are also seen when bacterial cells lacking RNase HI activity are grown and treated in the same way. All together, our results suggest that excess negative supercoiling promotes the formation of R-loops, which, in turn, inhibit RNA synthesis.

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