Cloned (Comment) | Organism |
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chromosomal DNA from the RNase J1 conditional mutant strain used to transform Bacillus subtilis host BG1 to erythromycin resistance. The RNase J1 conditional strain also contains plasmid pMAP65, which carries extra copies of the lacI gene. Preparation and transformation of Bacillus subtilis competent cell cultures. RNase J1 transcription under control of an IPTG-inducible promoter in the RNase J1 conditional mutant strain | Bacillus subtilis |
Organism | UniProt | Comment | Textmining |
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Bacillus subtilis | - |
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Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
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DELTAermC mRNA + H2O | DELTAermC mRNA decay is RNase J1 dependent. Decay-initiating endonuclease cleavage can occur at several sites near the 3' end. Preferred RNase J1 target sites are located in the downstream half of DELTAermC mRNA, located upstream of eSL1 (ermC stem-loop 1), between eSL1 and eSL2, and between eSL2 and the 3' transcription terminator. The putative endonuclease cleavages in the body of the message are not dependent on ribosome flow. Even in the absence of these sites, stability is further increased in a strain with reduced RNase J1, suggesting alternate pathways for decay that can include exonucleolytic decay from the 5' end | Bacillus subtilis | ? | - |
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Synonyms | Comment | Organism |
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RNase J1 | - |
Bacillus subtilis |
General Information | Comment | Organism |
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malfunction | DELTAermC mRNA shows increased stability in a RNase J1 mutant strain, that contains reduced level of RNase J1. Insertion of a strong stem-loop structure at +65 results in increased stability. Weakening this stem-loop structure results in reversion to wild-type stability. RNA fragments containing the 3' end are detected in a strain with reduced RNase J1 expression, but are undetectable in the wild-type. The 5' ends of these fragments map to the upstream side of predicted stem-loop structures, consistent with an impediment to RNase J1 5' exonuclease processivity. RNase J1 is involved even in decay of the RNA encoded by a 129-nt deletion construct, perhaps by a 59-to-39 exonucleolytic pathway or by cleavage at sites in the upstream half of the RNA. Deletion of the three target sites results in increased mRNA half-life (ca. 15 min) | Bacillus subtilis |