Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1984-3-21
|
pubmed:abstractText |
We have analyzed the nucleotide sequences and secondary structure required for the transcriptional inhibitory activity of the plus-strand leader RNA of vesicular stomatitis virus (VSV) in a reconstituted HeLa cell transcription system using the adenovirus-2 late promoter (LP) and virus-associated (VA) genes as templates. The New Jersey serotype (VSVNJ) leader and the leader of the Indiana serotype (VSVInd) both contain cleavage sites for the double-strand-specific ribonuclease V1, and these sites are consistent with the presence of a predicted AU-rich stem-loop structure. Studies in which the secondary structure was perturbed with the intercalating agent proflavin suggested that a stem-loop structure enhances the efficiency of transcription inhibition in the VSVNJ leader. Experiments using leader RNA fragments, a VSVInd cDNA derived from the 3' end of the genome, and synthetic oligodeoxynucleotide homologous to regions of the VSV leader indicated that the AU(AT)-rich center region of the VSV leader molecule is sufficient to inhibit DNA-dependent transcription directed by both polymerase II and III, but flanking nucleotide sequences are important for more efficient inhibition of transcription.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Restriction Enzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Oligodeoxyribonucleotides,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Viral
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0092-8674
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
36
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
533-43
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:6319029-Adenoviruses, Human,
pubmed-meshheading:6319029-Base Sequence,
pubmed-meshheading:6319029-Cloning, Molecular,
pubmed-meshheading:6319029-DNA,
pubmed-meshheading:6319029-DNA, Viral,
pubmed-meshheading:6319029-DNA Restriction Enzymes,
pubmed-meshheading:6319029-Genes, Viral,
pubmed-meshheading:6319029-HeLa Cells,
pubmed-meshheading:6319029-Humans,
pubmed-meshheading:6319029-Nucleic Acid Conformation,
pubmed-meshheading:6319029-Oligodeoxyribonucleotides,
pubmed-meshheading:6319029-Operon,
pubmed-meshheading:6319029-RNA, Viral,
pubmed-meshheading:6319029-Transcription, Genetic,
pubmed-meshheading:6319029-Vesicular stomatitis Indiana virus,
pubmed-meshheading:6319029-Vesiculovirus
|
pubmed:year |
1984
|
pubmed:articleTitle |
Nucleotide sequence and secondary structure of VSV leader RNA and homologous DNA involved in inhibition of DNA-dependent transcription.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
|