Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1988 Sep;62(9):3193-200.
doi: 10.1128/JVI.62.9.3193-3200.1988.

Multiple early transcripts and splicing of the Autographa californica nuclear polyhedrosis virus IE-1 gene

Affiliations

Multiple early transcripts and splicing of the Autographa californica nuclear polyhedrosis virus IE-1 gene

G E Chisholm et al. J Virol. 1988 Sep.

Abstract

The immediate-early IE-1 gene of Autographa californica nuclear polyhedrosis virus was cloned, and its nucleotide sequence was determined. Sequence analysis indicated that this gene would encode a protein of 582 amino acids with a predicted molecular weight of 66,822. Analysis of IE-1 gene expression during baculovirus infection identified two transcripts. One, 1.9 kilobases (kb), was expressed at constant steady-state levels throughout infection, whereas the other, 2.1 kb, was expressed only early in infection. Analysis of IE-1 cDNA clones demonstrated that the 2.1-kb transcript contained the entire 1.9-kb transcript (exon 1) plus an additional 5' end (exon 0). Genomic Southern analysis placed the exon 0 sequences on the EcoRI B fragment, 4 kilobase pairs upstream of exon 1. Sequencing of the upstream region identified an open reading frame whose 5' end was identical to the exon 0 sequences in the cDNAs. Examination of the genomic DNA sequences around the exon-exon junction revealed sequences similar to published consensus splice acceptor and donor sequences. This is the first example of splicing of any viral transcript during baculovirus infection.

PubMed Disclaimer

References

    1. J Virol. 1983 Mar;45(3):961-70 - PubMed
    1. J Virol. 1987 Jul;61(7):2091-9 - PubMed
    1. J Virol. 1982 Oct;44(1):199-208 - PubMed
    1. Proc Natl Acad Sci U S A. 1979 May;76(5):2232-5 - PubMed
    1. Proc Natl Acad Sci U S A. 1972 Jun;69(6):1408-12 - PubMed

LinkOut - more resources