Abstract
The region (retron-Ec67) required for the biosynthesis of a branched-RNA-linked multicopy single-stranded DNA (msDNA-Ec67) from a clinical isolate of Escherichia coli was mapped at a position equivalent to 19 min on the K-12 chromosome. The element containing the retron consisted of a unique 34-kilobase sequence that was flanked by direct repeats of a 26-base-pair sequence found in the K-12 chromosomal DNA. This suggests that the 34-kilobase element was probably integrated into the E. coli genome by a mechanism related to transposition or phage integration. In the 34-kilobase sequence an open reading frame of 285 residues was found, which displays 44% sequence identity with the E. coli Dam methylase. Interestingly, there are three GATC sequences, the site of Dam methylation, in the promoter region of the gene for reverse transcriptase.
MeSH Terms
Amino Acid Sequence
Base Sequence
Chromosome Mapping
Chromosomes, Bacterial
DNA Transposable Elements
DNA, Single-Stranded/genetics
Escherichia coli/genetics
Escherichia coli Proteins
Methyltransferases/genetics
Molecular Sequence Data
RNA-Directed DNA Polymerase/genetics
Restriction Mapping
Sequence Homology, Nucleic Acid
Site-Specific DNA-Methyltransferase (Adenine-Specific)
Chemicals
DNA Transposable Elements
DNA, Single-Stranded
Escherichia coli Proteins
Methyltransferases
Dam methyltransferase
Site-Specific DNA-Methyltransferase (Adenine-Specific)
dam protein, E coli
RNA-Directed DNA Polymerase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hsu M Y
Department of Biochemistry, Robert Wood Johnson Medical School, Rutgers, University of Medicine and Dentistry of New Jersey, Piscataway 08854.
Inouye M
Inouye S
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