Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:1888734rdf:typepubmed:Citationlld:pubmed
pubmed-article:1888734lifeskim:mentionsumls-concept:C1704689lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C0028953lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C0242958lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C1521970lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C0079866lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C1527177lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C1533691lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C0441513lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C1705542lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C0205171lld:lifeskim
pubmed-article:1888734lifeskim:mentionsumls-concept:C0441712lld:lifeskim
pubmed-article:1888734pubmed:issue36lld:pubmed
pubmed-article:1888734pubmed:dateCreated1991-10-17lld:pubmed
pubmed-article:1888734pubmed:abstractTextBy using a gene-targeted random DNA adduction approach, we have recently shown that chloroacetaldehyde, a metabolite of vinyl chloride, induces mutations predominantly at cytosines under conditions in which both ethenoadenine (epsilon A) and ethenocytosine (epsilon C) are formed. Although the observed mutational specificity of epsilon C suggested that it was a noninstructional lesion, the high efficiency of mutagenesis and an apparent lack of SOS dependence were reminiscent of mispairing lesions. To obtain more direct evidence showing that epsilon C has properties of a noninstructional mutagenic lesion, we have examined the in vitro template properties of a single epsilon C residue at a unique position in a synthetic oligonucleotide. The oligonucleotide was constructed by use of the following steps: (a) in vitro treatment of the pentameric oligodeoxyribonucleotide TTCTT with chloroacetaldehyde to convert the central cytosine to ethenocytosine; (b) purification and characterization of TT epsilon CTT; and (c) ligation of purified TT epsilon CTT to two decamers to create a 25 nt long oligodeoxyribonucleotide with a centrally located epsilon C residue. The template characteristics of epsilon C were examined by the annealing of end-labeled primers to the purified epsilon C-containing oligonucleotide and primer elongation by Escherichia coli DNA polymerase I in the presence of one or more nucleotide precursors. The elongation products were analyzed by high-resolution gel electrophoresis followed by autoradiography and quantitated by computing densitometry.(ABSTRACT TRUNCATED AT 250 WORDS)lld:pubmed
pubmed-article:1888734pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1888734pubmed:languageenglld:pubmed
pubmed-article:1888734pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1888734pubmed:citationSubsetIMlld:pubmed
pubmed-article:1888734pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1888734pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1888734pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1888734pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1888734pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1888734pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1888734pubmed:statusMEDLINElld:pubmed
pubmed-article:1888734pubmed:monthSeplld:pubmed
pubmed-article:1888734pubmed:issn0006-2960lld:pubmed
pubmed-article:1888734pubmed:authorpubmed-author:HumayunM ZMZlld:pubmed
pubmed-article:1888734pubmed:authorpubmed-author:SimhaDDlld:pubmed
pubmed-article:1888734pubmed:authorpubmed-author:PalejwalaV...lld:pubmed
pubmed-article:1888734pubmed:issnTypePrintlld:pubmed
pubmed-article:1888734pubmed:day10lld:pubmed
pubmed-article:1888734pubmed:volume30lld:pubmed
pubmed-article:1888734pubmed:ownerNLMlld:pubmed
pubmed-article:1888734pubmed:authorsCompleteYlld:pubmed
pubmed-article:1888734pubmed:pagination8727-35lld:pubmed
pubmed-article:1888734pubmed:dateRevised2007-11-14lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:meshHeadingpubmed-meshheading:1888734-...lld:pubmed
pubmed-article:1888734pubmed:year1991lld:pubmed
pubmed-article:1888734pubmed:articleTitleMechanisms of mutagenesis by exocyclic DNA adducts. Construction and in vitro template characteristics of an oligonucleotide bearing a single site-specific ethenocytosine.lld:pubmed
pubmed-article:1888734pubmed:affiliationDepartment of Microbiology and Molecular Genetics, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark 07103-2714.lld:pubmed
pubmed-article:1888734pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1888734pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1888734lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1888734lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1888734lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1888734lld:pubmed