Sequence and transcriptional analysis of an orf virus gene encoding ankyrinlike repeat sequences
- 1 February 1995
- journal article
- research article
- Published by Springer Nature in Virus Genes
- Vol. 9 (3) , 277-282
- https://doi.org/10.1007/bf01702883
Abstract
A 1608 bp region located approximately 5.0 kb from the left end of the orf virus (OV) genome (strain NZ2) was sequenced. The sequence revealed a single open reading frame designated G1L. The predicted amino acid sequence of G1L contained eight ankyrinlike repeat sequences. Transcriptional analysis of G1L showed it was transcribed towards the genome terminus during the early phase of infection. S1 nuclease and primer extension analyses showed that the transcriptional start site of the gene was located a short distance downstream from an A+T-rich sequence similar to a vaccinia virus early promoter.Keywords
This publication has 58 references indexed in Scilit:
- Modulation of Cardiac Sodium Channels by cAMP Receptors on the Myocyte SurfaceScience, 1991
- TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasmsPublished by Elsevier ,1991
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Cloning of the p50 DNA binding subunit of NF-κB: Homology to rel and dorsalCell, 1990
- The DNA binding subunit of NF-κB is identical to factor KBF1 and homologous to the rel oncogene productCell, 1990
- Structure of vaccinia virus early promotersJournal of Molecular Biology, 1989
- Characterization of vaccinia virus early promoters and evaluation of their informational contentJournal of Molecular Biology, 1987
- Orf virus replication in bovine testis cells: kinetics of viral DNA, polypeptide, and infectious virus production and analysis of virion polypeptidesArchiv für die gesamte Virusforschung, 1987
- Nucleotide sequence from the neurogenic locus Notch implies a gene product that shares homology with proteins containing EGF-like repeatsCell, 1985
- Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybridsCell, 1977