Promoters and processing sites within the transforming region of bovine papillomavirus type 1

The mRNAs present in bovine papillomavirus type 1 (BPV-1)-transformed C127 cells were studied by primer extension. The results show that two internal promoters are present in the E region of BPV-1 in addition to the previously identified promoter at coordinate 1 (H. Ahola, A. Stenlund, J. Moreno-López, and U. Pettersson, Nucleic Acids Res. 11:2639-2650, 1983). One, located at coordinate 31, generated a set of mRNAs with heterogeneous 5' ends, which may encode the major transforming protein of BPV-1, the E5 protein. The second promoter, which is located at coordinate 39, generates colinear mRNAs which encode either the E4 protein or a truncated form of the E2 protein. Unlike the cottontail rabbit papillomavirus (O. Danos, E. Georges, G. Orth, and M. Yaniv, J. Virol. 53:735-741, 1985), BPV-1 appears to lack a separate promoter for expression of the E7 protein. The major splice sites in the transforming region (E region) of the BPV-1 genome were also identified by nucleotide sequence analysis.

[1]  R. Schlegel,et al.  The E5 transforming gene of bovine papillomavirus encodes a small, hydrophobic polypeptide. , 1986, Science.

[2]  H. Zentgraf,et al.  Properties of intracellular bovine papillomavirus chromatin , 1986, Journal of virology.

[3]  D. DiMaio,et al.  Translation of open reading frame E5 of bovine papillomavirus is required for its transforming activity. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[4]  D. Lowy,et al.  E5 open reading frame of bovine papillomavirus type 1 encodes a transforming gene , 1986, Journal of virology.

[5]  U. Pettersson,et al.  Organization and expression of the transforming region from the European elk papillomavirus (EEPV). , 1986, Gene.

[6]  P. Howley,et al.  Dissociation of transforming and trans-activation functions for bovine papillomavirus type 1 , 1985, Nature.

[7]  U. Pettersson,et al.  Organization of early region 1B of human adenovirus type 2: identification of four differentially spliced mRNAs , 1985, Journal of virology.

[8]  U. Pettersson,et al.  Messenger RNAs from the transforming region of bovine papilloma virus type I. , 1985, Journal of molecular biology.

[9]  M. Yaniv,et al.  Fine structure of the cottontail rabbit papillomavirus mRNAs expressed in the transplantable VX2 carcinoma , 1985, Journal of virology.

[10]  P. Howley,et al.  Bovine papillomavirus contains multiple transforming genes. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[11]  H. Zentgraf,et al.  Origin of replication in episomal bovine papilloma virus type 1 DNA isolated from transformed cells. , 1984, The EMBO journal.

[12]  U. Pettersson,et al.  Rapid and quantitative recovery of DNA fragments from gels by displacement electrophoresis (isotachophoresis). , 1984, Biochimica et biophysica acta.

[13]  H. Pfister Biology and biochemistry of papillomaviruses. , 1984, Reviews of physiology, biochemistry and pharmacology.

[14]  U. Pettersson,et al.  European elk papillomavirus: characterization of the genome, induction of tumors in animals, and transformation in vitro , 1983, Journal of virology.

[15]  U. Pettersson,et al.  Sequences of bovine papillomavirus type 1 DNA--functional and evolutionary implications. , 1983, Nucleic acids research.

[16]  R. Contreras,et al.  Evidence for the direct involvement of DNA replication origin in synthesis of late SV40 RNA , 1982, Nature.

[17]  E. Ziff,et al.  Promoters and heterogeneous 5' termini of the messenger RNAs of adenovirus serotype 2. , 1981, Journal of molecular biology.

[18]  D. Lowy,et al.  Mouse cells transformed by bovine papillomavirus contain only extrachromosomal viral DNA sequences. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[19]  D. Lowy,et al.  In vitro tumorigenic transformation by a defined sub-genomic fragment of bovine papilloma virus DNA , 1980, Nature.

[20]  W. Gilbert,et al.  Sequencing end-labeled DNA with base-specific chemical cleavages. , 1980, Methods in enzymology.

[21]  G. Brawerman,et al.  A procedure for the isolation of mammalian messenger ribonucleic acid. , 1972, Biochemistry.