Red clover necrotic mosaic virus replication proteins accumulate at the endoplasmic reticulum

被引:78
作者
Turner, KA
Sit, TL
Callaway, AS
Allen, NS
Lommel, SA
机构
[1] N Carolina State Univ, Dept Plant Pathol, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Genet, Raleigh, NC 27695 USA
[3] N Carolina State Univ, Dept Bot, Raleigh, NC 27695 USA
基金
美国国家科学基金会; 美国国家航空航天局;
关键词
RCNMV; polymerase; green fluorescent protein; endoplasmic reticulum; co-localization; Tombusviridae; confocal microscopy;
D O I
10.1016/j.virol.2003.12.006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Red clover necrotic mosaic virus (RCNMV) encodes N-terminally overlapping proteins of 27 and 88 kDa (p27 and p88) known to be required for replication. Green fluorescent protein (GFP) fusions were used to visualize the location of p27 and p88 within Nicotiana benthamiana cells. GFP:p27 fusions localized to the endoplasmic reticulum (ER), co-localized with ER-targeted yellow fluorescent protein and caused membrane restructuring and proliferation. Cellular fractionation of virus-inoculated N. benthamiana leaves confirmed the association of p27 with ER membranes. GFP:p88 fusions also localized to the ER and co-localized with GFP:p27. Both fusion proteins co-localize to the cortical and cytoplasmic ER and were associated with invaginations of the nuclear envelope. Independent accumulation in, and perturbation of, the ER suggests that p27 and p88 function together in the replication complex. This is the first report of a member of the Tombusviridae replicating in association with the ER. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:276 / 290
页数:15
相关论文
共 65 条
[1]  
AHLQUIST P, 1994, ARCH VIROL, P135
[2]   INTERACTION OF ELONGATION-FACTOR 1 WITH AMINOACYLATED BROME MOSAIC-VIRUS AND TRANSFER-RNAS [J].
BASTIN, M ;
HALL, TC .
JOURNAL OF VIROLOGY, 1976, 20 (01) :117-122
[3]   ISOLATION AND CHARACTERIZATION OF AN RNA-DEPENDENT RNA-POLYMERASE FROM NICOTIANA-CLEVELANDII PLANTS INFECTED WITH RED-CLOVER NECROTIC MOSAIC DIANTHOVIRUS [J].
BATES, HJ ;
FARJAH, M ;
OSMAN, TAM ;
BUCK, KW .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :1483-1491
[4]   Stacks on tracks: the plant Golgi apparatus traffics on an actin/ER network [J].
Boevink, P ;
Oparka, K ;
Cruz, SS ;
Martin, B ;
Betteridge, A ;
Hawes, C .
PLANT JOURNAL, 1998, 15 (03) :441-447
[5]   A highly membrane-active peptide in Flock House virus: implications for the mechanism of nodavirus infection [J].
Bong, DT ;
Steinem, C ;
Janshoff, A ;
Johnson, JE ;
Ghadiri, MR .
CHEMISTRY & BIOLOGY, 1999, 6 (07) :473-481
[6]   KINETICS OF TOMATO GOLDEN MOSAIC-VIRUS DNA-REPLICATION AND COAT PROTEIN PROMOTER ACTIVITY IN NICOTIANA-TABACUM PROTOPLASTS [J].
BROUGH, CL ;
SUNTER, G ;
GARDINER, WE ;
BISARO, DM .
VIROLOGY, 1992, 187 (01) :1-9
[7]   The 5'-terminal region of a tombusvirus genome determines the origin of multivesicular bodies [J].
Burgyan, J ;
Rubino, L ;
Russo, M .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :1967-1974
[8]  
CALLAWAY AS, 1998, THESIS CORNELL U ITH
[9]   Cowpea mosaic virus infection induces a massive proliferation of endoplasmic reticulum but not Golgi membranes and is dependent on de novo membrane synthesis [J].
Carette, JE ;
Stuiver, M ;
Van Lent, J ;
Wellink, J ;
Van Kammen, AB .
JOURNAL OF VIROLOGY, 2000, 74 (14) :6556-6563
[10]   EXPRESSION OF POTYVIRAL POLYPROTEINS IN TRANSGENIC PLANTS REVEALS 3 PROTEOLYTIC ACTIVITIES REQUIRED FOR COMPLETE PROCESSING [J].
CARRINGTON, JC ;
FREED, DD ;
OH, CS .
EMBO JOURNAL, 1990, 9 (05) :1347-1353