Isolation of RNase H genes that are essential for growth of Bacillus subtilis 168

被引:79
|
作者
Itaya, M
Omori, A
Kanaya, S
Crouch, RJ
Tanaka, T
Kondo, K
机构
[1] Mitsubishi Kasei Inst Life Sci, Machida, Tokyo 1948511, Japan
[2] Osaka Univ, Grad Sch Engn, Suita, Osaka 5650871, Japan
[3] NICHHD, Genet Mol Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1128/JB.181.7.2118-2123.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 (28.1 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 rnhR 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.
引用
收藏
页码:2118 / 2123
页数:6
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