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PLANT PHYSIOLOGY , Vol 110, Issue 1 23-33, Copyright © 1996 by American Society of Plant Biologists
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PLANT-MICROBE AND PLANT-INSECT INTERACTIONS |
A Viral Movement Protein as a Nuclear Shuttle (The Geminivirus BR1 Movement Protein Contains Domains Essential for Interaction with BL1 and Nuclear Localization)
A. A. Sanderfoot, D. J. Ingham and S. G. Lazarowitz
Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801
For the nuclear replicating bipartite geminiviruses such as squash leaf
curl to systemically infect the host requires the active participation of
two virus-encoded movement proteins, BR1 and BL1. These act in a
cooperative manner to transport the viral single-stranded DNA genome from
its site of replication in the nucleus to the cell periphery (A.A.
Sanderfoot, S.G. Lazarowitz [1995] Plant Cell 7: 1185-1194). We have
proposed that BR1 functions as a nuclear shuttle protein, transporting the
viral single-stranded DNA to and from the nucleus as a complex that is
recognized by BL1 for movement to adjacent cells. To further investigate
this, we expressed BR1 mutants known to affect viral infectivity in
Spodoptera frugiperda insect cells and Nicotiana tabacum L. cv Xanthi
protoplasts and found these to be defective in either their nuclear
targeting or their ability to be redirected to the cell periphery when
co-expressed with BL1. Translational fusions to [beta]-glucuronidase and
alanine-scanning mutagenesis further demonstrated that the C-terminal 86
amino acids of BR1 contains a domain(s) essential for its interaction with
BL1 and identified two nuclear localization signals within the N-terminal
113 residues of BR1. These nuclear localization signals were precisely
located within distinct 16- and 22-peptide segments of BR1. These studies
support and extend our model for squash leaf curl virus movement, showing
that BR1 has a domain structure, with an N-terminal region required for
nuclear targeting and a C-terminal region required for its interaction with
BL1.
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