Synthesis of minus-strand copies of a viral transgene during viral infections of transgenic plants

Virus Res. 2006 Dec;122(1-2):171-4. doi: 10.1016/j.virusres.2006.05.009. Epub 2006 Sep 11.

Abstract

Viral transgenes designed to provide resistance to specific plant viruses frequently consist of the coat protein gene and a contiguous 3' untranslated region (3'UTR) of viral origin. In many RNA viruses the viral 3'UTR establishes a recognition and initiation site for viral RNA replication. Thus the transgenic transcript may contain a functional virus replication site. Experiments were designed to determine if a challenging virus would recognize this replication site on a nuclear derived transcript and synthesize the complementary RNA. These data demonstrate that upon infection by a virus that recognizes the viral replication site, a full-length complement of the transgenic transcript is produced. In these experiments the replication complex of Brome Mosaic bromovirus recognized the transgenic transcript derived from a Cowpea Chlorotic Mottle bromovirus transgene. The resulting RNA may contribute to RNA recombination events.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Bromovirus / genetics*
  • Bromovirus / physiology
  • Electrophoresis, Agar Gel
  • Plants, Genetically Modified / virology*
  • RNA, Complementary / biosynthesis*
  • RNA, Viral / biosynthesis*
  • Recombination, Genetic
  • Reverse Transcriptase Polymerase Chain Reaction
  • Virus Replication

Substances

  • RNA, Complementary
  • RNA, Viral