A viral suppressor of gene silencing in plants

被引:665
作者
Anandalakshmi, R [1 ]
Pruss, GJ [1 ]
Ge, X [1 ]
Marathe, R [1 ]
Mallory, AC [1 ]
Smith, TH [1 ]
Vance, VB [1 ]
机构
[1] Univ S Carolina, Dept Biol Sci, Columbia, SC 29208 USA
关键词
D O I
10.1073/pnas.95.22.13079
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gene silencing is an important but little understood regulatory mechanism in plants. Here we report that a viral sequence, initially identified as a mediator of synergistic viral disease, acts to suppress the establishment of both transgene-induced and virus-induced posttranscriptional gene silencing. The viral suppressor of silencing comprises the 5'-proximal region of the tobacco etch potyviral genomic RNA encoding P1, helper component-proteinase (HC-Pro) and a small part of P3, and is termed the P1/HC-Pro sequence. A reversal of silencing assay was used to assess the effect of the P1/HC-Pro sequence on transgenic tobacco plants (line T4) that are posttranscriptionally silenced for the uidA reporter gene. Silencing was lifted in offspring of T4 crosses with four independent transgenic lines expressing P1/HC-Pro, but not in offspring of control crosses. Viral vectors were used to assess the effect of P1/HC-Pro expression on virus-induced gene silencing (VIGS), The ability of a potato virus X vector expressing green fluorescent protein to induce silencing of a green fluorescent protein transgene was eliminated or greatly reduced when P1/HC-Pro was expressed from the same vector or from coinfecting potato virus X vectors. Expression of the HC-Pro coding sequence alone was sufficient to suppress virus-induced gene silencing, and the HC-Pro protein product was required for the suppression. This discovery points to the role of gene silencing as a natural antiviral defense system in plants and offers different approaches to elucidate the molecular basis of gene silencing.
引用
收藏
页码:13079 / 13084
页数:6
相关论文
共 35 条
[1]   Transcriptional and posttranscriptional plant gene silencing in response to a pathogen [J].
Al-Kaff, NS ;
Covey, SN ;
Kreike, MM ;
Page, AM ;
Pinder, R ;
Dale, PJ .
SCIENCE, 1998, 279 (5359) :2113-2115
[2]   HIGH-EFFICIENCY TRANSFORMATION OF CULTURED TOBACCO CELLS [J].
AN, GH .
PLANT PHYSIOLOGY, 1985, 79 (02) :568-570
[3]   MUTATIONAL ANALYSIS OF THE HELPER COMPONENT-PROTEINASE GENE OF A POTYVIRUS - EFFECTS OF AMINO-ACID SUBSTITUTIONS, DELETIONS, AND GENE REPLACEMENT ON VIRULENCE AND APHID TRANSMISSIBILITY [J].
ATREYA, CD ;
PIRONE, TP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11919-11923
[4]   SITE-DIRECTED MUTATIONS IN THE POTYVIRUS HC-PRO GENE AFFECT HELPER COMPONENT ACTIVITY, VIRUS ACCUMULATION, AND SYMPTOM EXPRESSION IN INFECTED TOBACCO PLANTS [J].
ATREYA, CD ;
ATREYA, PL ;
THORNBURY, DW ;
PIRONE, TP .
VIROLOGY, 1992, 191 (01) :106-111
[5]  
Baulcombe DC, 1996, PLANT CELL, V8, P1833, DOI 10.1105/tpc.8.10.1833
[6]   JELLYFISH GREEN FLUORESCENT PROTEIN AS A REPORTER FOR VIRUS-INFECTIONS [J].
BAULCOMBE, DC ;
CHAPMAN, S ;
CRUZ, SS .
PLANT JOURNAL, 1995, 7 (06) :1045-1053
[7]   Cosuppression comes to the animals [J].
Bingham, PM .
CELL, 1997, 90 (03) :385-387
[8]   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
[9]  
CHAPMAN S, 1992, PLANT J, V2, P549
[10]   Plants combat infection by gene silencing [J].
Covey, SN ;
AlKaff, NS ;
Langara, A ;
Turner, DS .
NATURE, 1997, 385 (6619) :781-782