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Spliced Early MRNAs of Simian Virus 40

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Specialty Science
Date 1978 Mar 1
PMID 206891
Citations 387
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Abstract

Biochemical methods are presented for determining the structure of spliced RNAs present in cells at low concentrations. Two cytoplasmic spliced viral RNAs were detected in CV-1 cells during the early phase of simian virus 40 (SV40) infection. One is 2200 nucleotides in length and is composed of two parts, 330 and 1900 nucleotides, mapping from approximately 0.67 to approximately 0.60 and from approximately 0.54 to approximately 0.14, respectively, on the standard viral map. The other is 2500 nucleotides long and also is composed of two parts, 630 and 1900 nucleotides mapping from approximately 0.67 to approximately 0.54 and from approximately 0.54 to approximately 0.14, respectively. Correlation of the structure of these mRNAs with the structure of the early SV40 proteins, small T antigen (17,000 daltons) and large T antigen (90,000 daltons), determined by others suggests that: (i) translation of the 2500-nucleotide mRNA yields small T antigen; (ii) translation of the 2200-nucleotide mRNA proceeds through the splice point in the RNA to produce large T antigen (and thus large T antigen is encoded in two separate regions of the viral genome); and (iii) the DNA sequences between approximately 0.67 and approximately 0.60 present in both mRNAs are translated in the same reading frame in both mRNAs to yield two separate gene products that have the same NH(2)-terminal sequence. Therefore, expression of the early SV40 genes is partially controlled at the level of splicing of RNAs.

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References
1.
Rigby P, Dieckmann M, Rhodes C, Berg P . Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol. 1977; 113(1):237-51. DOI: 10.1016/0022-2836(77)90052-3. View

2.
Feunteun J, SOMPAYRAC L, Fluck M, Benjamin T . Localization of gene functions in polyoma virus DNA. Proc Natl Acad Sci U S A. 1976; 73(11):4169-73. PMC: 431371. DOI: 10.1073/pnas.73.11.4169. View

3.
Casey J, Davidson N . Rates of formation and thermal stabilities of RNA:DNA and DNA:DNA duplexes at high concentrations of formamide. Nucleic Acids Res. 1977; 4(5):1539-52. PMC: 343772. DOI: 10.1093/nar/4.5.1539. View

4.
Schaffhausen B, Silver J, BENJAMIN T . Tumor antigen(s) in cell productively infected by wild-type polyoma virus and mutant NG-18. Proc Natl Acad Sci U S A. 1978; 75(1):79-83. PMC: 411187. DOI: 10.1073/pnas.75.1.79. View

5.
CRAWFORD L, Cole C, Smith A, Paucha E, Tegtmeyer P, Rundell K . Organization and expression of early genes of simian virus 40. Proc Natl Acad Sci U S A. 1978; 75(1):117-21. PMC: 411195. DOI: 10.1073/pnas.75.1.117. View