The small cysteine-rich protein P14 of beet necrotic yellow vein virus regulates accumulation of RNA 2 in cis and coat protein in trans

Virology. 1995 Jun 20;210(1):73-81. doi: 10.1006/viro.1995.1318.

Abstract

The effect of null mutations of the small cysteine-rich protein P14 encoded by RNA 2 of beet necrotic yellow vein virus has been investigated using in vitro transcripts of viral RNA to infect Chenopodium quinoa protoplasts. The P14 mutations down-regulated RNA 2 accumulation by approximately 10- to 50-fold. Accumulation of minus-strand RNA 2 was also diminished but RNA 1 accumulation was much less affected. The inhibition of RNA 2 accumulation could not be complemented in trans by providing P14 from another source (either a second molecule of RNA 2 or an RNA 3-based replicon) containing and expressing the P14 gene. The P14 null mutations dramatically inhibited accumulation of viral coat protein, which is encoded by the 5'-proximal gene on RNA 2, but this effect could be complemented in trans, indicating that it occurs by a mechanism distinct from that affecting RNA 2 accumulation. Transient expression experiments were also carried out in which a plasmid expressing P14 and plasmids expressing a reporter gene placed downstream of potential translational control sequences (the 5'-noncoding sequences of RNAs 2, 3, or 4) were introduced into C. quinoa or Nicotiana tabacum leaves by microprojectile bombardment. Coexpression of P14 produced a 3- to 4-fold stimulation of reporter gene expression levels for all the constructs. The lack of sequence specificity suggests that this phenomenon is not directly related to the RNA 2-specific stimulation of coat protein accumulation observed in a viral infection.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Capsid / biosynthesis*
  • DNA Primers
  • Frameshift Mutation
  • Gene Expression Regulation, Viral*
  • Genes, Viral*
  • Molecular Sequence Data
  • Mutagenesis, Insertional
  • Nicotiana / virology
  • Plant Viruses / genetics
  • Plant Viruses / metabolism*
  • Plants, Toxic
  • Point Mutation
  • Polymerase Chain Reaction
  • RNA Viruses / genetics
  • RNA Viruses / metabolism*
  • RNA, Viral / biosynthesis*
  • Restriction Mapping
  • Transcription, Genetic
  • Vegetables / virology
  • Viral Proteins / metabolism*

Substances

  • DNA Primers
  • RNA, Viral
  • Viral Proteins
  • small cysteine-rich protein P14, plant virus