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| pubmed-article:1701261 | lifeskim:mentions | umls-concept:C0035379 | lld:lifeskim |
| pubmed-article:1701261 | lifeskim:mentions | umls-concept:C0542341 | lld:lifeskim |
| pubmed-article:1701261 | lifeskim:mentions | umls-concept:C0012868 | lld:lifeskim |
| pubmed-article:1701261 | lifeskim:mentions | umls-concept:C0679058 | lld:lifeskim |
| pubmed-article:1701261 | lifeskim:mentions | umls-concept:C1547699 | lld:lifeskim |
| pubmed-article:1701261 | lifeskim:mentions | umls-concept:C2700640 | lld:lifeskim |
| pubmed-article:1701261 | lifeskim:mentions | umls-concept:C0057098 | lld:lifeskim |
| pubmed-article:1701261 | lifeskim:mentions | umls-concept:C0066880 | lld:lifeskim |
| pubmed-article:1701261 | pubmed:issue | 23 | lld:pubmed |
| pubmed-article:1701261 | pubmed:dateCreated | 1991-1-16 | lld:pubmed |
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| pubmed-article:1701261 | pubmed:abstractText | 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. | lld:pubmed |
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| pubmed-article:1701261 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1701261 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1701261 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:1701261 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1701261 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:1701261 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:1701261 | pubmed:author | pubmed-author:InouyeMM | lld:pubmed |
| pubmed-article:1701261 | pubmed:author | pubmed-author:HsuM YMY | lld:pubmed |
| pubmed-article:1701261 | pubmed:author | pubmed-author:InouyeSS | lld:pubmed |
| pubmed-article:1701261 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1701261 | pubmed:volume | 87 | lld:pubmed |
| pubmed-article:1701261 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1701261 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1701261 | pubmed:pagination | 9454-8 | lld:pubmed |
| pubmed-article:1701261 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:1701261 | pubmed:year | 1990 | lld:pubmed |
| pubmed-article:1701261 | pubmed:articleTitle | Retron for the 67-base multicopy single-stranded DNA from Escherichia coli: a potential transposable element encoding both reverse transcriptase and Dam methylase functions. | lld:pubmed |
| pubmed-article:1701261 | pubmed:affiliation | Department of Biochemistry, Robert Wood Johnson Medical School, Rutgers, University of Medicine and Dentistry of New Jersey, Piscataway 08854. | lld:pubmed |
| pubmed-article:1701261 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1701261 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:1701261 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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