Double-stranded RNA binding may be a general plant RNA viral strategy to suppress RNA silencing

被引:229
作者
Merai, Zsuzsanna
Kerenyi, Zoltan
Kertesz, Sandor
Magna, Melinda
Lakatos, Lorant
Silhavy, Daniel
机构
[1] Agr Biotechnol Ctr, H-2101 Godollo, Hungary
[2] Eotvos Lorand Univ, Dept Genet, Budapest, Hungary
关键词
D O I
10.1128/JVI.01963-05
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In plants, RNA silencing (RNA interference) is an efficient antiviral system, and therefore successful virus infection requires suppression of silencing. Although many viral silencing suppressors have been identified, the molecular basis of silencing suppression is poorly understood. It is proposed that various suppressors inhibit RNA silencing by targeting different steps. However, as double-stranded RNAs (dsRNAs) play key roles in silencing, it was speculated that dsRNA binding might be a general silencing suppression strategy. Indeed, it was shown that the related aureusvirus P14 and tombusvirus P19 suppressors are dsRNA-binding proteins. Interestingly, P14 is a size-independent dsRNA-binding protein, while P19 binds only 21-nucleotide ds-sRNAs (small dsRNAs having 2-nucleotide 3' overhangs), the specificity determinant of the silencing system. Much evidence supports the idea that P19 inhibits silencing by sequestering silencing-generated viral ds-sRNAs. In this study we wanted to test the hypothesis that dsRNA binding is a general silencing suppression strategy. Here we show that many plant viral silencing suppressors bind dsRNAs. Beet yellows virus Peanut P21, clump virus P15, Barley stripe mosaic virus gamma B, and Tobacco etch virus HC-Pro, like P19, bind ds-sRNAs size-selectively, while Turnip crinkle virus CP is a size-independent dsRNA-binding protein, which binds long dsRNAs; as well as ds-sRNAs. We propose that size-selective ds-sRNA-binding suppressors inhibit silencing by sequestering viral ds-sRNAs, whereas size-independent dsRNA-binding suppressors inactivate silencing by sequestering long dsRNA precursors of viral sRNAs and/or by binding ds-sRNAs. The findings that many unrelated silencing suppressors bind dsRNA suggest that dsRNA binding is a general silencing suppression strategy which has evolved independently many times.
引用
收藏
页码:5747 / 5756
页数:10
相关论文
共 72 条
[1]   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
[2]   RNA silencing in plants [J].
Baulcombe, D .
NATURE, 2004, 431 (7006) :356-363
[3]   RNA silencing [J].
Baulcombe, D .
TRENDS IN BIOCHEMICAL SCIENCES, 2005, 30 (06) :290-293
[4]   Crystal structure of p19 -: a universal suppressor of RNA silencing [J].
Baulcombe, DC ;
Molnár, A .
TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (06) :279-281
[5]   Evidence that HIV-1 encodes an siRNA and a suppressor of RNA silencing [J].
Bennasser, Y ;
Le, SY ;
Benkirane, M ;
Jeang, KT .
IMMUNITY, 2005, 22 (05) :607-619
[6]   Histidine-tagging and purification of tobacco etch potyvirus helper component protein [J].
Blanc, S ;
Dolja, VV ;
Llave, C ;
Pirone, TP .
JOURNAL OF VIROLOGICAL METHODS, 1999, 77 (01) :11-15
[7]   The N-terminal 85 amino acids of the Barley stripe mosaic virus γb pathogenesis protein contain three zinc-binding motifs [J].
Bragg, JN ;
Lawrence, DM ;
Jackson, AO .
JOURNAL OF VIROLOGY, 2004, 78 (14) :7379-7391
[8]   RETRACTED: Viral pathogenicity determinants are suppressors of transgene silencing in Nicotiana benthamiana (Retracted article. See vol. 34, pg. 2595, 2015) [J].
Brigneti, G ;
Voinnet, O ;
Li, WX ;
Ji, LH ;
Ding, SW ;
Baulcombe, DC .
EMBO JOURNAL, 1998, 17 (22) :6739-6746
[9]   The influenza A virus NS1 protein binds small interfering RNAs and suppresses RNA silencing in plants [J].
Bucher, E ;
Hemmes, H ;
de Haan, P ;
Goldbach, R ;
Prins, M .
JOURNAL OF GENERAL VIROLOGY, 2004, 85 :983-991
[10]   Dual modes of RNA-silencing suppression by flock house virus protein B2 [J].
Chao, JA ;
Lee, JH ;
Chapados, BR ;
Debler, EW ;
Schneemann, A ;
Williamson, JR .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2005, 12 (11) :952-957