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Ribonuclease M5 Has Few, If Any, mRNA Substrates in Bacillus subtilis

机译:核糖核酸酶M5在枯草芽孢杆菌中几乎没有mRNA底物

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In Bacillus subtilis, maturation of 5S rRNA is catalyzed by an enzyme called RNase M5. We searched for potential mRNA substrates for RNase M5 by gene array technology, based on the premise that most endonucleolytic cleavages have an effect on the stability of RNA and hence on steady-state levels of expression. Only a handful of genes had significantly altered expression in rnmV mutants compared to wild-type strains that could subsequently be confirmed by Northern blotting. The effect of RNase M5 on the expression of the best candidates, the odhAB and sucCD operons, is indirect, by a mechanism we do not yet understand. We show that an effect of RNase M5 on the expression of the remaining candidate, ctsR, is due to the failure to process the 5S rRNA contained in the rrnW lying directly upstream. We thus conclude that RNase M5 has very few or possibly no mRNA substrates in B. subtilis.
机译:枯草芽孢杆菌中,5S rRNA的成熟被称为RNase M5的酶催化。我们基于大多数内切核酸酶裂解对RNA的稳定性以及因此对表达的稳态水平有影响的前提,通过基因阵列技术搜索了RNase M5的潜在mRNA底物。与野生型菌株相比,只有少数基因在 rnmV 突变体中的表达发生了显着改变,随后可以通过Northern印迹法进行确认。 RNase M5对最佳候选蛋白 odhAB sucCD 操纵子表达的影响是间接的,目前尚不清楚。我们表明,RNase M5对其余候选表达 ctsR 的影响是由于未能处理直接位于上游的 rrnW 中包含的5S rRNA。因此,我们得出结论,RNase M5在emB中几乎没有或可能没有mRNA底物。枯草

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