TY - JOUR
T1 - Overexpression of RNase H partially complements the growth defect of an Escherichia coli ΔtopA mutant
T2 - R-loop formation is a major problem in the absence of DNA topoisomerase I
AU - Drolet, Marc
AU - Phoenix, Pauline
AU - Menzel, Rolf
AU - Massé, Eric
AU - Liu, Leroy F.
AU - Crouch, Robert J.
PY - 1995/4/11
Y1 - 1995/4/11
N2 - Previous biochemical studies have suggested a role for bacterial DNA topoisomerase (TOPO) I in the suppression of R-loop formation during transcription. In this report, we present several pieces of genetic evidence to support a model in which R-loop formation is dynamically regulated during transcription by activities of multiple DNA TOPOs and RNase H. In addition, our results suggest that events leading to the serious growth problems in the absence of DNA TOPO I are linked to R-loop formation. We show that the overexpression of RNase H, an enzyme that degrades the RNA moiety of an R loop, can partially compensate for the absence of DNA TOPO I. We also note that a defect in DNA gyrase can correct several phenotypes associated with a mutation in the rnhA gene, which encodes the major RNase H activity. In addition, we found that a combination of topA and rnhA mutations is lethal.
AB - Previous biochemical studies have suggested a role for bacterial DNA topoisomerase (TOPO) I in the suppression of R-loop formation during transcription. In this report, we present several pieces of genetic evidence to support a model in which R-loop formation is dynamically regulated during transcription by activities of multiple DNA TOPOs and RNase H. In addition, our results suggest that events leading to the serious growth problems in the absence of DNA TOPO I are linked to R-loop formation. We show that the overexpression of RNase H, an enzyme that degrades the RNA moiety of an R loop, can partially compensate for the absence of DNA TOPO I. We also note that a defect in DNA gyrase can correct several phenotypes associated with a mutation in the rnhA gene, which encodes the major RNase H activity. In addition, we found that a combination of topA and rnhA mutations is lethal.
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U2 - 10.1073/pnas.92.8.3526
DO - 10.1073/pnas.92.8.3526
M3 - Article
C2 - 7536935
AN - SCOPUS:0028966185
SN - 0027-8424
VL - 92
SP - 3526
EP - 3530
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 8
ER -