Abstract
DNA replication of the plasmid ColE1 and its relatives is controlled mainly by a small plasmid-encoded transcript known as RNA11. We have studied the conformation of RNA1 molecules from two related but compatible plasmids, ColE1 and RSF1030, using T1 ribonuclease, S1 nuclease, cobra venom nuclease, and diethyl pyrocarbonate modification as probes for secondary structure. Both RNA1 molecules contain three double-stranded stems, three single-stranded loops, and an exposed 5' tail. All loops in both molecules show similar sensitivities to the probes used, as do stems 1 and 3. The region comprising stem 2 of each RNA1 molecule contains the most sequence differences as well as the most structural changes of any region in the two molecules. The structure of the RNA1 molecule encoded by a recessive high copy number mutant of ColE1 was also investigated. Structural alterations involving the first stem and loop of the molecule are proposed to be responsible for the inability of the mutant RNA1 to function in vivo.
MeSH Terms
Base Sequence
DNA Replication
Diethyl Pyrocarbonate
Endonucleases
Nucleic Acid Conformation
Plasmids
RNA
Ribonuclease T1
Ribonucleases
Single-Strand Specific DNA and RNA Endonucleases
Transcription Factors
Transcription, Genetic
Chemicals
Transcription Factors
RNA
Endonucleases
Ribonucleases
Ribonuclease T1
Single-Strand Specific DNA and RNA Endonucleases
Diethyl Pyrocarbonate
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tamm J
Polisky B
References (19)
19 references, click to expand
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