The novel C5 protein from tomato yellow leaf curl virus is a virulence factor and suppressor of gene silencing

被引:41
作者
Zhao, Siwen [1 ]
Gong, Pan [1 ]
Ren, Yanxiang [1 ]
Liu, Hui [2 ]
Li, Hao [1 ]
Li, Fangfang [1 ]
Zhou, Xueping [1 ,2 ]
机构
[1] Chinese Acad Agr Sci, Inst Plant Protect, State Key Lab Biol Plant Dis & Insect Pests, Beijing 100193, Peoples R China
[2] Zhejiang Univ, Inst Biotechnol, State Key Lab Rice Biol, Hangzhou 310058, Zhejiang, Peoples R China
来源
STRESS BIOLOGY | 2022年 / 2卷 / 01期
基金
中国国家自然科学基金;
关键词
Tomato yellow leaf curl virus; C5; Hypersensitive response; Post-transcriptional gene silencing; Transcriptional gene silencing; Pathogenicity determinant; FUNCTIONAL-ANALYSIS; COAT PROTEIN; DNA-A; BEGOMOVIRUS; GEMINIVIRUS; AL2;
D O I
10.1007/s44154-022-00044-3
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
Tomato yellow leaf curl virus (TYLCV) is known to encode 6 canonical viral proteins. Our recent study revealed that TYLCV also encodes some additional small proteins with potential virulence functions. The fifth ORF of TYLCV in the complementary sense, which we name C5, is evolutionarily conserved, but little is known about its expression and function during viral infection. Here, we confirmed the expression of the TYLCV C5 by analyzing the promoter activity of its upstream sequences and by detecting the C5 protein in infected cells by using a specific custom-made antibody. Ectopic expression of C5 using a potato virus X (PVX) vector resulted in severe mosaic symptoms and higher virus accumulation levels followed by a burst of reactive oxygen species (ROS) in Nicotiana benthamiana plants. C5 was able to effectively suppress local and systemic post-transcriptional gene silencing (PTGS) induced by single-stranded GFP but not double-stranded GFP, and reversed the transcriptional gene silencing (TGS) of GFP. Furthermore, the mutation of C5 in TYLCV inhibited viral replication and the development of disease symptoms in infected plants. Transgenic overexpression of C5 could complement the virulence of a TYLCV infectious clone encoding a dysfunctional C5. Collectively, this study reveals that TYLCV C5 is a pathogenicity determinant and RNA silencing suppressor, hence expanding our knowledge of the functional repertoire of the TYLCV proteome.
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页数:13
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