J Gen Virol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Frischmuth, T.
Right arrow Articles by Stanley, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Frischmuth, T.
Right arrow Articles by Stanley, J.
Agricola
Right arrow Articles by Frischmuth, T.
Right arrow Articles by Stanley, J.

Journal of General Virology, Vol 79, 1265-1271, Copyright © 1998 by Society for General Microbiology


ARTICLES

Recombination between viral DNA and the transgenic coat protein gene of African cassava mosaic geminivirus

T Frischmuth and J Stanley
Universitat Stuttgart, Biologisches Institut, Lehrstuhl fur Molekularbiologie und Virologie der Pflanzen, Germany. thomas.frischmuth@po.uni-stuttgart.de

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, recombination had occurred between the mutant viral DNA and the integrated construct DNA, resulting in the production of recombinant virus progeny with 'wild-type' characteristics. No reversion of mutant to 'wild-type' virus was observed in pJC1-transformed plants. Recombinant virus from several transgenic plants was analysed by PCR and parts of DNA A of virus progeny were cloned. Sequence analysis revealed that only a few nucleotides were changed from the published sequence.


This article has been cited by other articles:


Home page
J. Virol.Home page
K. Kittelmann, P. Rau, B. Gronenborn, and H. Jeske
Plant Geminivirus Rep Protein Induces Rereplication in Fission Yeast
J. Virol., July 1, 2009; 83(13): 6769 - 6778.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
Y. Hong, J. Stanley, and R. van Wezel
Novel System for the Simultaneous Analysis of Geminivirus DNA Replication and Plant Interactions in Nicotiana benthamiana
J. Virol., December 15, 2003; 77(24): 13315 - 13322.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
M. Varrelmann, L. Palkovics, and E. Maiss
Transgenic or Plant Expression Vector-Mediated Recombination of Plum Pox Virus
J. Virol., August 15, 2000; 74(16): 7462 - 7469.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1998 by the Society for General Microbiology.