Alternative transcriptional initiation as a novel mechanism for regulating expression of a baculovirus trans activator

J Virol. 1993 Oct;67(10):5833-42. doi: 10.1128/JVI.67.10.5833-5842.1993.

Abstract

In this report, we show that the Orgyia pseudotsugata nuclear polyhedrosis virus p34 gene, which is homologous to the Autographa californica nuclear polyhedrosis virus PE-38 gene, is a trans activator. The predicted p34 protein contains a number of motifs that are similar to those found in other eukaryotic transcriptional trans activators, including a putative zinc finger DNA-binding domain, a glutamine-rich domain, and a leucine zipper. Northern (RNA) blot analysis showed that the p34 gene is expressed as a 1.1-kb mRNA from 1 to 48 h postinfection and as a 0.7-kb mRNA from 18 to 120 h postinfection. Mapping of these transcripts showed that they were 3' coterminal but initiated at different 5' start sites. The 1.1-kb transcript initiates at a baculovirus early gene motif (CACAGT) and encodes the entire p34 open reading frame (ORF). The 0.7-kb transcript initiates at a baculovirus late gene start site (GTAAG) internal to the p34 ORF. Western blot (immunoblot) analysis using p34 antisera showed that the 0.7-kb transcript is translated as an amino-terminally truncated 20-kDa form of the full length 34-kDa protein. Functional analysis indicated that the 34-kDa protein transcriptionally trans activates the IE-2 promoter whereas the 20-kDa protein does not. Therefore, p34 produces two functionally different proteins from the same ORF, using the novel mechanism of alternative transcriptional initiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Amino Acid Sequence
  • Animals
  • Baculoviridae / genetics
  • Baculoviridae / metabolism*
  • Base Sequence
  • Blotting, Northern
  • Blotting, Western
  • Cell Line
  • Cloning, Molecular
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / genetics
  • Enhancer Elements, Genetic
  • Escherichia coli / genetics
  • Gene Expression Regulation, Viral*
  • Genes, Viral
  • Insecta
  • Molecular Sequence Data
  • Moths
  • Oligodeoxyribonucleotides
  • RNA, Messenger / genetics
  • RNA, Messenger / isolation & purification
  • RNA, Messenger / metabolism
  • RNA, Viral / genetics
  • RNA, Viral / isolation & purification
  • Restriction Mapping
  • Trans-Activators / biosynthesis*
  • Transcription, Genetic*
  • Viral Structural Proteins / genetics

Substances

  • DNA-Binding Proteins
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • RNA, Viral
  • Trans-Activators
  • Viral Structural Proteins