In vivo complementation of infectious transcripts from mutant tobacco mosaic virus cDNAs in transgenic plants.

Abstract:

:A full-length cDNA clone of the U1 (common) strain of tobacco mosaic virus (TMV) was constructed, and highly infectious transcripts were produced in vitro using bacteriophage T7 RNA polymerase. Frameshift mutations designed to cause premature termination of translation were introduced into either the 30-kDa movement protein (MP) gene or the coat protein (CP) gene. The MP-frameshift mutant was unable to locally or systemically infect inoculated tobacco plants. However, inoculation of transgenic tobacco plants that expressed a wild-type TMV MP gene resulted in both local and systemic viral infection. The CP-frameshift mutant, although unable to move systemically in nontransformed tobacco, exhibited systemic movement in transgenic plants that expressed a wild-type TMV CP gene. Transgenic tobacco plants that expressed the appropriate wild-type TMV gene were thus able to complement, in trans, mutant viruses lacking a functional MP or CP gene.

journal_name

Virology

journal_title

Virology

authors

Holt CA,Beachy RN

doi

10.1016/0042-6822(91)90475-q

subject

Has Abstract

pub_date

1991-03-01 00:00:00

pages

109-17

issue

1

eissn

0042-6822

issn

1096-0341

journal_volume

181

pub_type

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