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
[1]   TRANSIENT TRANSFORMATION OF ARABIDOPSIS LEAF PROTOPLASTS - A VERSATILE EXPERIMENTAL SYSTEM TO STUDY GENE-EXPRESSION [J].
ABEL, S ;
THEOLOGIS, A .
PLANT JOURNAL, 1994, 5 (03) :421-427
[2]   The beet yellows closterovirus p65 homologue of HSP70 chaperones has ATPase activity associated with its conserved N-terminal domain but does not interact with unfolded protein chains [J].
Agranovsky, AA ;
Folimonova, SY ;
Folimonov, AS ;
Denisenko, ON ;
Zinovkin, RA .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :535-542
[3]   Cell-to-cell movement of potato virus X is associated with a change in the size-exclusion limit of plasmodesmata in trichome cells of Nicotiana clevelandii [J].
Angell, SM ;
Davies, C ;
Baulcombe, DC .
VIROLOGY, 1996, 216 (01) :197-201
[4]   PLANT VIRUS-SPECIFIC TRANSPORT FUNCTION AND RESISTANCE OF PLANTS TO VIRUSES [J].
ATABEKOV, JG ;
DOROKHOV, YL .
ADVANCES IN VIRUS RESEARCH, 1984, 29 :313-364
[5]   Mutational analysis of the cowpea mosaic virus movement protein [J].
Bertens, P ;
Wellink, J ;
Goldbach, R ;
van Kammen, A .
VIROLOGY, 2000, 267 (02) :199-208
[6]   Host suppressors in Arabidopsis thaliana of mutations in the movement protein gene of Cauliflower mosaic virus [J].
Callaway, AS ;
Huang, Z ;
Howell, SH .
MOLECULAR PLANT-MICROBE INTERACTIONS, 2000, 13 (05) :512-519
[7]  
Carrington JC, 1996, PLANT CELL, V8, P1669, DOI 10.1105/tpc.8.10.1669
[8]   Interaction between the tobacco mosaic virus movement protein and host cell pectin methylesterases is required for viral cell-to-cell movement [J].
Chen, MH ;
Sheng, JS ;
Hind, G ;
Handa, AK ;
Citovsky, V .
EMBO JOURNAL, 2000, 19 (05) :913-920
[9]   PROTEIN-INTERACTION CLONING IN YEAST - IDENTIFICATION OF MAMMALIAN PROTEINS THAT REACT WITH THE LEUCINE ZIPPER OF JUN [J].
CHEVRAY, PM ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :5789-5793
[10]   GENE-I, A POTENTIAL CELL-TO-CELL MOVEMENT LOCUS OF CAULIFLOWER MOSAIC-VIRUS, ENCODES AN RNA-BINDING PROTEIN [J].
CITOVSKY, V ;
KNORR, D ;
ZAMBRYSKI, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) :2476-2480