1998
DOI: 10.1099/0022-1317-79-5-1265
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Recombination between viral DNA and the transgenic coat protein gene of African cassava mosaic geminivirus.

Abstract: Nicotiana benthamiana was transformed with three different constructs (pCRA1, pCRA2 and pJC1) containing the coat protein coding sequence of African cassava mosaic virus (ACMV). Transformed plants were inoculated with a coat protein deletion mutant of ACMV that induces mild systemic symptoms in control plants. Several inoculated plants of transgenic lines CRA1/3, CRA1/4, CRA2/1 and CRA2/2 developed severe systemic symptoms typical of ACMV. DNA analysis revealed that, in these plants,

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Cited by 49 publications
(25 citation statements)
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“…Thus, Rep-mediated initiation, termination of replication at two different transgenic origins, and circularization of the nascent strand will produce a replicon containing a single intact copy of the origin. A previous investigation with a similar construct based on an ACMV DNA-A deletion mutant with flanking origins of replication failed to mobilize a 1,900-bp replicon in this way (14). The reason for this different behaviour is unclear but presumably resides in the difference in composition or size of the transgenes that could affect the mobilization, replication, and/or stability of the replicons.…”
Section: Discussionmentioning
confidence: 95%
“…Thus, Rep-mediated initiation, termination of replication at two different transgenic origins, and circularization of the nascent strand will produce a replicon containing a single intact copy of the origin. A previous investigation with a similar construct based on an ACMV DNA-A deletion mutant with flanking origins of replication failed to mobilize a 1,900-bp replicon in this way (14). The reason for this different behaviour is unclear but presumably resides in the difference in composition or size of the transgenes that could affect the mobilization, replication, and/or stability of the replicons.…”
Section: Discussionmentioning
confidence: 95%
“…Features such as failure in gap repair, extended lifetime of open circular DNA (pararetrovirus episomal particles), or recombination between free ends of "virus" and plant DNA have been suggested by Jakowitsch et al (1999) as facilitators of integration. When a pararetrovirus (Cauliflower mosaic virus, CaMV) deficient in gene function is introduced into a plant containing a translational transactivator transgene, the virus can utilise the gene product to complete the infection cycle (Kirá ly et al, 1998), a similar phenomenon to that was seen with geminiviruses (Frischmuth and Stanley, 1998).…”
Section: Discussionmentioning
confidence: 97%
“…Several examples of recombination between a virus and its homologous transgene have been reported (Adair and Kearney, 2000;Borja et al, 1999;Frischmuth and Stanley, 1998;Gal et al, 1992Gal et al, , 1996Allison, 1994, 1996;Schoelz and Wintermantel, 1993;Turturo et al, 2008;Wintermantel and Schoelz, 1996). In most cases, a defective virus was used such that recombination would restore full infectivity and thus confer a significant selective advantage on the recombinant.…”
Section: Hgt From Gm Plants To Virusesmentioning
confidence: 99%