Isolation of RNase H Genes That Are Essential for Growth of Bacillus subtilis 168

Author:

Itaya Mitsuhiro1,Omori Akira1,Kanaya Shigenori2,Crouch Robert J.3,Tanaka Teruo1,Kondo Kanae1

Affiliation:

1. Mitsubishi-Kasei Institute of Life Sciences, Machida-shi, Tokyo 194-8511,1 and

2. Material and Life Science, Graduate School of Engineering, Osaka University, Osaka 565-0871,2 Japan, and

3. Laboratory of Molecular Genetics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-27903

Abstract

ABSTRACT Two genes encoding functional RNase H (EC 3.1.26.4 ) were isolated from a gram-positive bacterium, Bacillus subtilis 168. Two DNA clones exhibiting RNase H activities both in vivo and in vitro were obtained from a B. subtilis DNA library. One (28.2 kDa) revealed high similarity to Escherichia coli RNase HII, encoded by the rnhB gene. The other (33.9 kDa) was designated rnhC and encodes B. subtilis RNase HIII. The B. subtilis genome has an rnhA homologue, the product of which has not yet shown RNase H activity. Analyses of all three B. subtilis genes revealed that rnhB and rnhC cannot be simultaneously inactivated. This observation indicated that in B. subtilis both the rnhB and rnhC products are involved in certain essential cellular processes that are different from those suggested by E. coli rnh mutation studies. Sequence conservation between the rnhB and rnhC genes implies that both originated from a single ancestral RNase H gene. The roles of bacterial RNase H may be indicated by the single rnhC homologue in the small genome of Mycoplasma species.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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