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Effect of RNase III on the size of bacteriophage T7 lysozyme mRNA
Abstract:
The size of lysozyme mRNA from T7-infected E. coli RNase III+ and RNase III- strains was analyzed by sucrose gradient sedimentation, dimethylsulfoxide (Me2SO) sucorse gradient sedimentation, and preparative gel electrophoresis. Each technique revealed a similar size distribution of multiple lysozyme mRNA's. Analysis by preparative gel electrophoresis of RNA extracted after infection of Escherichia coli Bst (RNase III+) separated lysozyme mRNA into six peaks of activity ranging in size from 0.2 x 10(6) to 1.9 x 10(6) daltons. Four well-resolved major peaks of activity were detected, having apparent molecular weights of approximately 0.61 x 10(6), 0.76 x 10(6), 0.92 x 10(6), and 1.3 x 10(6). A broad band of activity, with a molecular weight range from 0.2 x 10(6) to 0.37 x 10(6), was also present, and a sixth peak of activity was sometimes observed that migrates with a mobility corresponding to a molecular weight of 1.9 x 10(6). Judging from their molecular weight as estimated by electrophoresis, most, if not all, of the lysozyme mRNA's were polycistronic. The RNA extracted after infection of an RNase III- host contained a more heterogeneous collection of lysozyme mRNA's. In addition to lysozyme mRNA activity on RNAs with molecular weights between 0.2 x 10(6) and 1.9 x 10(6), RNA species with molecular weights estimated at 4 x 10(6) to 5 x 10(6) were also detected. The data indicate that RNase III processes at least some of the primary lysozyme transcripts. The multiple lysozyme mRNA's represent discrete RNA species rather than aggregates because analysis of the size of lysozyme mRNA under completely denaturing conditions, in Me2SO, produced a similar size distribution of lysozyme mRNAs. Also, treatment of RNA with 90% Me2SO, which separates the strands of a completely double-stranded RNA, did not significantly alter the electrophoretic mobility of the lysozyme mRNA.
Insights
RNase III enzyme processes lysozyme mRNA in E. coli, generating multiple discrete mRNA species. This processing is crucial for generating functional messenger RNA molecules from primary transcripts.
Area of Science:
- Molecular Biology
- Microbiology
- Genetics
Background:
- Lysozyme mRNA size and processing in bacteriophage T7-infected Escherichia coli are not fully understood.
- The role of RNase III in processing bacterial mRNA transcripts requires further investigation.
Purpose of the Study:
- To analyze the size distribution of lysozyme mRNA produced in RNase III-positive (RNase III+) and RNase III-negative (RNase III-) E. coli strains infected with T7.
- To investigate the role of RNase III in the processing of T7 lysozyme mRNA.
Main Methods:
- Sucrose gradient sedimentation
- Dimethylsulfoxide (Me2SO) sucrose gradient sedimentation
- Preparative gel electrophoresis
Main Results:
- Multiple lysozyme mRNA species were detected in both RNase III+ and RNase III- strains, with sizes ranging from 0.2 x 10(6) to 1.9 x 10(6) daltons.
- RNase III+ strains showed six distinct peaks of lysozyme mRNA activity, with four major peaks between 0.61 x 10(6) and 1.3 x 10(6) daltons.
- RNase III- strains exhibited a more heterogeneous collection of lysozyme mRNAs, including larger species (4 x 10(6) to 5 x 10(6) daltons), suggesting RNase III processing of primary transcripts.
Conclusions:
- RNase III plays a role in processing T7 lysozyme mRNA precursors into discrete mRNA species.
- The observed multiple lysozyme mRNAs are distinct RNA molecules, not aggregates, as confirmed by denaturing conditions.
- Most, if not all, detected lysozyme mRNAs are likely polycistronic based on their molecular weights.