| pubmed-article:1310768 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1310768 | lifeskim:mentions | umls-concept:C0014080 | lld:lifeskim |
| pubmed-article:1310768 | lifeskim:mentions | umls-concept:C0035736 | lld:lifeskim |
| pubmed-article:1310768 | lifeskim:mentions | umls-concept:C1519249 | lld:lifeskim |
| pubmed-article:1310768 | lifeskim:mentions | umls-concept:C0678935 | lld:lifeskim |
| pubmed-article:1310768 | lifeskim:mentions | umls-concept:C0678594 | lld:lifeskim |
| pubmed-article:1310768 | lifeskim:mentions | umls-concept:C0013879 | lld:lifeskim |
| pubmed-article:1310768 | lifeskim:mentions | umls-concept:C1880177 | lld:lifeskim |
| pubmed-article:1310768 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:1310768 | pubmed:dateCreated | 1992-3-16 | lld:pubmed |
| pubmed-article:1310768 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1310768 | pubmed:abstractText | The nucleotide sequence of the 5' nontranslated region of encephalomyocarditis virus (EMCV-Rueckert) was determined, and a consensus RNA structural model for this sequence (850 bases) and three other poly(C)-containing cardioviruses (mengovirus, EMCV-B, and EMCV-D) was created through reiterative use of a minimum-free-energy folding algorithm. The RNA elements within this region which contribute to translation of EMCV proteins were mapped in cell-free reactions programmed with cDNA-derived RNA transcripts. The data provide evidence that stem-loop motifs I, J and K, formed by viral bases 451 to 785, are important components of cap-independent translation. In contrast to other reports, a minimal role for stem-loop H (bases 406 to 444) in translational activity is indicated. Small 5' nontranslated region fragments (bases 667 to 797) containing the J and K motifs proved strong competitive inhibitors when added to cell-free reactions programmed with exogenous capped or uncapped mRNAs. The putative sequestering of required translational factors by this segment clearly contributes to translational activity, but also suggests a possible competitive mechanism for the down regulation of host protein synthesis during viral infection. | lld:pubmed |
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| pubmed-article:1310768 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1310768 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1310768 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:1310768 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1310768 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:1310768 | pubmed:issn | 0022-538X | lld:pubmed |
| pubmed-article:1310768 | pubmed:author | pubmed-author:PalmenbergA... | lld:pubmed |
| pubmed-article:1310768 | pubmed:author | pubmed-author:HoffmanM AMA | lld:pubmed |
| pubmed-article:1310768 | pubmed:author | pubmed-author:DukeG MGM | lld:pubmed |
| pubmed-article:1310768 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1310768 | pubmed:volume | 66 | lld:pubmed |
| pubmed-article:1310768 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1310768 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1310768 | pubmed:pagination | 1602-9 | lld:pubmed |
| pubmed-article:1310768 | pubmed:dateRevised | 2010-9-7 | lld:pubmed |
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| pubmed-article:1310768 | pubmed:year | 1992 | lld:pubmed |
| pubmed-article:1310768 | pubmed:articleTitle | Sequence and structural elements that contribute to efficient encephalomyocarditis virus RNA translation. | lld:pubmed |
| pubmed-article:1310768 | pubmed:affiliation | Institute for Molecular Virology, University of Wisconsin, Madison 53706. | lld:pubmed |
| pubmed-article:1310768 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1310768 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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