Identification of Arabidopsis proteins that interact with the cauliflower mosaic virus (CaMV) movement protein

被引:51
作者
Huang, Z [1 ]
Andrianov, VM [1 ]
Han, Y [1 ]
Howell, SH [1 ]
机构
[1] Cornell Univ, Boyce Thompson Inst, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
plant virus; virus movement; yeast 2-hybrid system; rab acceptor; fluorescence resonance energy transfer;
D O I
10.1023/A:1012491913431
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene I of cauliflower mosaic virus (CaMV) encodes a protein that is required for virus movement. The CaMV movement protein (MP) was used in a yeast 2-hybrid system to screen an Arabidopsis cDNA library for cDNAs encoding MP-interacting (MPI) proteins. Three different clones were found encoding proteins (MPI1, -2 and -7) that interact with the N-terminal third of the CaMV MP. The interaction in the 2-hybrid system between MPI7 and CaMV MP mutants correlated with the infectivity of the mutants. A non-infectious MP mutant, ER2A, with two amino acid changes in the N-terminal third of the MP failed to interact with MPI7, while an infectious second-site mutant, that differed from ER2A by only a single amino acid change, interacted in the 2-hybrid system. MPI7 is encoded by a member of a large, but diverse gene family in Arabidopsis. MPI7 is related in sequence, size and hydropathy profile to mammalian proteins (such as rat PRA1) described as a rab acceptor. The gene encoding MPI7 is expressed widely is Arabidopsis plants, and in transgenic plants the MPI7:GFP fusion protein is localized in the cytoplasm, concentrated in punctate spots. In protoplasts transfected with CFP:MP and MPI7:YFP, CFP:MP colocalized to some of the sites where MPI7:YFP is expressed. At these sites, fluorescence resonance energy transfer (FRET) between fluorophores was observed indicating an interaction in planta between the CaMV MP and MPI7.
引用
收藏
页码:663 / 675
页数:13
相关论文
共 78 条
[41]   THE SUBCELLULAR LOCATION OF THE GENE-1 PRODUCT OF CAULIFLOWER MOSAIC-VIRUS IS CONSISTENT WITH A FUNCTION ASSOCIATED WITH VIRUS SPREAD [J].
LINSTEAD, PJ ;
HILLS, GJ ;
PLASKITT, KA ;
WILSON, IG ;
HARKER, CL ;
MAULE, AJ .
JOURNAL OF GENERAL VIROLOGY, 1988, 69 :1809-1818
[42]   SELECTIVE TRAFFICKING OF KNOTTED1 HOMEODOMAIN PROTEIN AND ITS MESSENGER-RNA THROUGH PLASMODESMATA [J].
LUCAS, WJ ;
BOUCHEPILLON, S ;
JACKSON, DP ;
NGUYEN, L ;
BAKER, L ;
DING, B ;
HAKE, S .
SCIENCE, 1995, 270 (5244) :1980-1983
[43]   TANSLEY REVIEW NO. 58 PLASMODESMATA AND THE SUPRACELLULAR NATURE OF PLANTS [J].
LUCAS, WJ ;
DING, B ;
VANDERSCHOOT, C .
NEW PHYTOLOGIST, 1993, 125 (03) :435-476
[44]   PLASMODESMATA - INTERCELLULAR CHANNELS FOR MACROMOLECULAR TRANSPORT IN PLANTS [J].
LUCAS, WJ .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (05) :673-680
[45]   Bcl-2 and Bax interactions in mitochondria probed with green fluorescent protein and fluorescence resonance energy transfer [J].
Mahajan, NP ;
Linder, K ;
Berry, G ;
Gordon, GW ;
Heim, R ;
Herman, B .
NATURE BIOTECHNOLOGY, 1998, 16 (06) :547-552
[46]   Isolation and characterization of a dual prenylated Rab and VAMP2 receptor [J].
Martincic, I ;
Peralta, ME ;
Ngsee, JK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (43) :26991-26998
[47]   Functional interaction of phytochrome B and cryptochrome 2 [J].
Más, P ;
Devlin, PF ;
Panda, S ;
Kay, SA .
NATURE, 2000, 408 (6809) :207-211
[48]  
McLean Barbara Gail, 1993, Trends in Microbiology, V1, P105, DOI 10.1016/0966-842X(93)90116-9
[49]   The '30K' superfamily of viral movement proteins [J].
Melcher, U .
JOURNAL OF GENERAL VIROLOGY, 2000, 81 :257-266
[50]   Plasmodesmal cell-to-cell transport of proteins and nucleic acids [J].
Mezitt, LA ;
Lucas, WJ .
PLANT MOLECULAR BIOLOGY, 1996, 32 (1-2) :251-273