Abstract
To test whether the promoters of two immediate-early genes from frog virus 3 were similar in nucleotide sequence, we have cloned and sequenced an immediate-early gene encoding an infected-cell mRNA of 489 kilodaltons (ICR489) and have shown that the protein product of this gene is approximately 46 kilodaltons. The 5' and 3' ends of the transcripts from this gene, as determined by mung bean nuclease analysis, were microheterogeneous. The promoter region was subcloned upstream from a promoterless chloramphenicol acetyltransferase gene, forming the recombinant plasmid pBS489CAT. As with the previously sequenced frog virus 3 immediate-early gene encoding ICR169, expression of chloramphenicol acetyltransferase in transfected cells required activation by a virion-associated protein. Although the promoter region of the gene encoding ICR489 contained TATA, CAAT, and GC motifs similar to those of typical eucaryotic promoters, it showed no significant homology to the ICR169 promoter, indicating that the concomitant temporal expression of these two genes is not due to similar promoter sequences.
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- Aubertin A. M., Hirth C., Travo C., Nonnenmacher H., Kirn A. Preparation and properties of an inhibitory extract from frog virus 3 particles. J Virol. 1973 May;11(5):694–701. doi: 10.1128/jvi.11.5.694-701.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benoist C., O'Hare K., Breathnach R., Chambon P. The ovalbumin gene-sequence of putative control regions. Nucleic Acids Res. 1980 Jan 11;8(1):127–142. doi: 10.1093/nar/8.1.127. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Berk A. J., Sharp P. A. Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybrids. Cell. 1977 Nov;12(3):721–732. doi: 10.1016/0092-8674(77)90272-0. [DOI] [PubMed] [Google Scholar]
- Bina-Stein M., Thoren M., Salzman N., Thomspon J. A. Rapid sequence determination of late simian virus 40 16S mRNA leader by using inhibitors of reverse transcriptase. Proc Natl Acad Sci U S A. 1979 Feb;76(2):731–735. doi: 10.1073/pnas.76.2.731. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chandler P. M. The use of single-stranded phage DNAs in hybrid arrest and release translation. Anal Biochem. 1982 Nov 15;127(1):9–16. doi: 10.1016/0003-2697(82)90137-3. [DOI] [PubMed] [Google Scholar]
- Chow L. T., Roberts J. M., Lewis J. B., Broker T. R. A map of cytoplasmic RNA transcripts from lytic adenovirus type 2, determined by electron microscopy of RNA:DNA hybrids. Cell. 1977 Aug;11(4):819–836. doi: 10.1016/0092-8674(77)90294-x. [DOI] [PubMed] [Google Scholar]
- Corden J., Wasylyk B., Buchwalder A., Sassone-Corsi P., Kedinger C., Chambon P. Promoter sequences of eukaryotic protein-coding genes. Science. 1980 Sep 19;209(4463):1406–1414. doi: 10.1126/science.6251548. [DOI] [PubMed] [Google Scholar]
- Dynan W. S., Tjian R. The promoter-specific transcription factor Sp1 binds to upstream sequences in the SV40 early promoter. Cell. 1983 Nov;35(1):79–87. doi: 10.1016/0092-8674(83)90210-6. [DOI] [PubMed] [Google Scholar]
- Goorha R. Frog virus 3 requires RNA polymerase II for its replication. J Virol. 1981 Jan;37(1):496–499. doi: 10.1128/jvi.37.1.496-499.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goorha R., Murti K. G. The genome of frog virus 3, an animal DNA virus, is circularly permuted and terminally redundant. Proc Natl Acad Sci U S A. 1982 Jan;79(2):248–252. doi: 10.1073/pnas.79.2.248. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goorha R., Willis D. B., Granoff A. Macromolecular synthesis in cells infected by frog virus 3. XII. Viral regulatory proteins in transcriptional and post-transcriptional controls. J Virol. 1979 Nov;32(2):442–448. doi: 10.1128/jvi.32.2.442-448.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gorman C. M., Moffat L. F., Howard B. H. Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells. Mol Cell Biol. 1982 Sep;2(9):1044–1051. doi: 10.1128/mcb.2.9.1044. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Graham F. L., van der Eb A. J. A new technique for the assay of infectivity of human adenovirus 5 DNA. Virology. 1973 Apr;52(2):456–467. doi: 10.1016/0042-6822(73)90341-3. [DOI] [PubMed] [Google Scholar]
- Gravell M., Naegele R. F. Nongenetic reactivation of frog polyhedral cytoplasmic deoxyribovirus (PCDV). Virology. 1970 Jan;40(1):170–174. doi: 10.1016/0042-6822(70)90390-9. [DOI] [PubMed] [Google Scholar]
- Green M. R., Roeder R. G. Definition of a novel promoter for the major adenovirus-associated virus mRNA. Cell. 1980 Nov;22(1 Pt 1):231–242. doi: 10.1016/0092-8674(80)90171-3. [DOI] [PubMed] [Google Scholar]
- Guir J., Braunwald J., Kirn A. Inhibition of host-specific DNA and RNA synthesis in KB cells following infection with frog virus 3. J Gen Virol. 1971 Sep;12(3):293–301. doi: 10.1099/0022-1317-12-3-293. [DOI] [PubMed] [Google Scholar]
- Klymkowsky M. W., Miller R. H., Lane E. B. Morphology, behavior, and interaction of cultured epithelial cells after the antibody-induced disruption of keratin filament organization. J Cell Biol. 1983 Feb;96(2):494–509. doi: 10.1083/jcb.96.2.494. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Langridge J., Langridge P., Bergquist P. L. Extraction of nucleic acids from agarose gels. Anal Biochem. 1980 Apr;103(2):264–271. doi: 10.1016/0003-2697(80)90266-3. [DOI] [PubMed] [Google Scholar]
- Lee M. H., Willis D. B. Restriction endonuclease mapping of the frog virus 3 genome. Virology. 1983 Apr 15;126(1):317–327. doi: 10.1016/0042-6822(83)90481-6. [DOI] [PubMed] [Google Scholar]
- Lehrach H., Diamond D., Wozney J. M., Boedtker H. RNA molecular weight determinations by gel electrophoresis under denaturing conditions, a critical reexamination. Biochemistry. 1977 Oct 18;16(21):4743–4751. doi: 10.1021/bi00640a033. [DOI] [PubMed] [Google Scholar]
- Martin J. P., Aubertin A. M., Kirn A. Expression of frog virus 3 early genes after ultraviolet irradiation. Virology. 1982 Oct 30;122(2):402–410. doi: 10.1016/0042-6822(82)90239-2. [DOI] [PubMed] [Google Scholar]
- Mathis D. J., Chambon P. The SV40 early region TATA box is required for accurate in vitro initiation of transcription. Nature. 1981 Mar 26;290(5804):310–315. doi: 10.1038/290310a0. [DOI] [PubMed] [Google Scholar]
- McKnight J. L., Kristie T. M., Roizman B. Binding of the virion protein mediating alpha gene induction in herpes simplex virus 1-infected cells to its cis site requires cellular proteins. Proc Natl Acad Sci U S A. 1987 Oct;84(20):7061–7065. doi: 10.1073/pnas.84.20.7061. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McKnight S. L., Kingsbury R. C., Spence A., Smith M. The distal transcription signals of the herpesvirus tk gene share a common hexanucleotide control sequence. Cell. 1984 May;37(1):253–262. doi: 10.1016/0092-8674(84)90321-0. [DOI] [PubMed] [Google Scholar]
- Naegele R. F., Granoff A. Viruses and renal carcinoma of Rana pipiens. XI. Isolation of frog virus 3 temperature-sensitive mutants; complementation and genetic recombination. Virology. 1971 May;44(2):286–295. doi: 10.1016/0042-6822(71)90260-1. [DOI] [PubMed] [Google Scholar]
- Nevins J. R. The pathway of eukaryotic mRNA formation. Annu Rev Biochem. 1983;52:441–466. doi: 10.1146/annurev.bi.52.070183.002301. [DOI] [PubMed] [Google Scholar]
- Parker B. A., Stark G. R. Regulation of simian virus 40 transcription: sensitive analysis of the RNA species present early in infections by virus or viral DNA. J Virol. 1979 Aug;31(2):360–369. doi: 10.1128/jvi.31.2.360-369.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Raghow R., Willis D. B., Granoff A. Macromolecular synthesis in cells infected by frog virus 3. XIII. Cell-free translation of immediate early viral mRNAs. Virology. 1980 Jan 30;100(2):495–497. doi: 10.1016/0042-6822(80)90541-3. [DOI] [PubMed] [Google Scholar]
- Sanger F. Determination of nucleotide sequences in DNA. Science. 1981 Dec 11;214(4526):1205–1210. doi: 10.1126/science.7302589. [DOI] [PubMed] [Google Scholar]
- Tham T. N., Mesnard J. M., Tondre L., Aubertin A. M. Mapping of the gene coding for the major late structural polypeptide on the frog virus 3 genome. J Gen Virol. 1986 Feb;67(Pt 2):301–308. doi: 10.1099/0022-1317-67-2-301. [DOI] [PubMed] [Google Scholar]
- Willis D. B. DNA sequences required for trans-activation of an immediate-early frog virus 3 gene. Virology. 1987 Nov;161(1):1–7. doi: 10.1016/0042-6822(87)90164-4. [DOI] [PubMed] [Google Scholar]
- Willis D. B., Goorha R., Chinchar V. G. Macromolecular synthesis in cells infected by frog virus 3. Curr Top Microbiol Immunol. 1985;116:77–106. doi: 10.1007/978-3-642-70280-8_5. [DOI] [PubMed] [Google Scholar]
- Willis D. B., Goorha R., Granoff A. DNA methyltransferase induced by frog virus 3. J Virol. 1984 Jan;49(1):86–91. doi: 10.1128/jvi.49.1.86-91.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Willis D. B., Goorha R., Granoff A. Nongenetic reactivation of frog virus 3 DNA. Virology. 1979 Oct 30;98(2):476–479. doi: 10.1016/0042-6822(79)90572-5. [DOI] [PubMed] [Google Scholar]
- Willis D. B., Goorha R., Miles M., Granoff A. Macromolecular synthesis in cells infected by frog virus 3. VII. Transcriptional and post-transcriptional regulation of virus gene expression. J Virol. 1977 Oct;24(1):326–342. doi: 10.1128/jvi.24.1.326-342.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Willis D. B., Granoff A. Macromolecular synthesis in cells infected by frog virus 3. IX. Two temporal classes of early viral RNA. Virology. 1978 May 15;86(2):443–453. doi: 10.1016/0042-6822(78)90084-3. [DOI] [PubMed] [Google Scholar]
- Willis D. B., Granoff A. Macromolecular synthesis in cells infected with frog virus 3. V. The absence of polyadenylic acid in the majority of frog virus 3-specific mRNA species. Virology. 1976 Sep;73(2):543–547. doi: 10.1016/0042-6822(76)90417-7. [DOI] [PubMed] [Google Scholar]
- Willis D. B., Granoff A. trans activation of an immediate-early frog virus 3 promoter by a virion protein. J Virol. 1985 Nov;56(2):495–501. doi: 10.1128/jvi.56.2.495-501.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Willis D., Foglesong D., Granoff A. Nucleotide sequence of an immediate-early frog virus 3 gene. J Virol. 1984 Dec;52(3):905–912. doi: 10.1128/jvi.52.3.905-912.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]




