| pubmed-article:8093641 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:8093641 | lifeskim:mentions | umls-concept:C1709694 | lld:lifeskim |
| pubmed-article:8093641 | lifeskim:mentions | umls-concept:C0220104 | lld:lifeskim |
| pubmed-article:8093641 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:8093641 | pubmed:dateCreated | 1993-2-18 | lld:pubmed |
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| pubmed-article:8093641 | pubmed:abstractText | Northern blot analysis of the Epstein-Barr virus DNA polymerase mRNA identified two discrete sizes of virally encoded polymerase transcripts, 5.08 kb detected in strains P3HR1, Raji, W-91, and FF-41 and 3.7 kb detected solely in the prototype B95-8 strain. 3' S1-nuclease mapping and analysis of cDNA sequence generated by RNA-based PCR demonstrated that the 3.7-kb polymerase mRNA from B95-8 terminates 484 base pairs downstream of the open reading frame in a region of the genome remarkable for its lack of an apparent polyadenylylation signal. Moreover, between the cleavage point and the poly(A) tract of the cDNAs are a series of inserted nucleotides, mostly adenosine and uridine residues of unknown origin. A similar analysis of the 3' terminus of the 5.0-kb mRNA from the other cell lines revealed that polyadenylylation occurs 1.4 kb downstream of the B95-8 terminus. This region is deleted in B95-8, which accounts for the alternate upstream terminus used in B95-8. Like the 3.7-kb terminus, the 5.0-kb terminus lacks a canonical polyadenylylation signal, but contains a rarely used UAUAAA sequence 32 bp upstream of the poly(A) tail. These results indicate that the mRNA encoded by the Epstein-Barr virus DNA polymerase gene is polyadenylylated at two different termini without the use of canonical signals, raising the possibility of involvement of a virus-encoded factor in 3' processing of this message. | lld:pubmed |
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| pubmed-article:8093641 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:8093641 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:8093641 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8093641 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:8093641 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:8093641 | pubmed:author | pubmed-author:AdamsM DMD | lld:pubmed |
| pubmed-article:8093641 | pubmed:author | pubmed-author:PaganoJ SJS | lld:pubmed |
| pubmed-article:8093641 | pubmed:author | pubmed-author:FurnariF BFB | lld:pubmed |
| pubmed-article:8093641 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8093641 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:8093641 | pubmed:volume | 90 | lld:pubmed |
| pubmed-article:8093641 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8093641 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8093641 | pubmed:pagination | 378-82 | lld:pubmed |
| pubmed-article:8093641 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:8093641 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:8093641 | pubmed:articleTitle | Unconventional processing of the 3' termini of the Epstein-Barr virus DNA polymerase mRNA. | lld:pubmed |
| pubmed-article:8093641 | pubmed:affiliation | Department of Microbiology, University of North Carolina, Chapel Hill 27599. | lld:pubmed |
| pubmed-article:8093641 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8093641 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:8093641 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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