Zhang Dong-Xiu, Spiering Martin J, Nuss Donald L
Institute for Bioscience and Biotechnology Research and Department of Cell Biology and Molecular Genetics, University of Maryland, Rockville, Maryland, United States of America.
PLoS One. 2014 Sep 30;9(9):e108653. doi: 10.1371/journal.pone.0108653. eCollection 2014.
An inducible RNA-silencing pathway, involving a single Dicer protein, DCL2, and a single Argonaute protein, AGL2, was recently shown to serve as an effective antiviral defense response in the chestnut blight fungus Cryphonectria parasitica. Eukaryotic RNA-dependent RNA polymerases (RdRPs) are frequently involved in transcriptional and posttranscriptional gene silencing and antiviral defense. We report here the identification and characterization of four RdRP genes (rdr1-4) in the C. parasitica genome. Sequence relationships with other eukaryotic RdRPs indicated that RDR1 and RDR2 were closely related to QDE-1, an RdRP involved in RNA silencing ("quelling") in Neurospora crassa, whereas RDR3 was more closely related to the meiotic silencing gene SAD-1 in N. crassa. The RdRP domain of RDR4, related to N. crassa RRP-3 of unknown function, was truncated and showed evidence of alternative splicing. Similar to reports for dcl2 and agl2, the expression levels for rdr3 and rdr4 increased after hypovirus CHV-1/EP713 infection, while expression levels of rdr1 and rdr2 were unchanged. The virus-responsive induction patterns for rdr3 and rdr4 were altered in the Δdcl2 and Δagl2 strains, suggesting some level of interaction between rdr3 and rdr4 and the dcl2/agl2 silencing pathway. Single rdr gene knockouts Δrdr1-4, double knockouts Δrdr1/2, Δrdr2/3, Δrdr1/3, and a triple knockout, Δrdr1/2/3, were generated and evaluated for effects on fungal phenotype, the antiviral defense response, viral RNA recombination activity and transposon expression. None of the single or multiple rdr knockout strains displayed any phenotypic differences from the parental strains with or without viral infection or any significant changes in viral RNA accumulation or recombination activity or transposon RNA accumulation, indicating no detectable contribution by the C. parasitica rdr genes to these processes.
最近研究表明,在栗疫病菌(Cryphonectria parasitica)中,一条涉及单个Dicer蛋白(DCL2)和单个AGO蛋白(AGL2)的可诱导RNA沉默途径,是一种有效的抗病毒防御反应。真核生物RNA依赖的RNA聚合酶(RdRP)经常参与转录和转录后基因沉默以及抗病毒防御。我们在此报告了栗疫病菌基因组中四个RdRP基因(rdr1 - 4)的鉴定和特征。与其他真核生物RdRP的序列关系表明,RDR1和RDR2与粗糙脉孢菌(Neurospora crassa)中参与RNA沉默(“抑制”)的RdRP QDE - 1密切相关,而RDR3与粗糙脉孢菌中的减数分裂沉默基因SAD - 1关系更密切。RDR4的RdRP结构域与功能未知的粗糙脉孢菌RRP - 3相关,被截断且存在可变剪接的证据。与dcl2和agl2的报道相似,rdr3和rdr4的表达水平在低毒病毒CHV - 1/EP713感染后升高,而rdr1和rdr2的表达水平未改变。在Δdcl2和Δagl2菌株中,rdr3和rdr4的病毒反应诱导模式发生改变,表明rdr3和rdr4与dcl2/agl2沉默途径之间存在一定程度的相互作用。构建了单个rdr基因敲除株Δrdr1 - 4、双敲除株Δrdr1/2、Δrdr2/3、Δrdr1/3以及三敲除株Δrdr1/2/3,并评估它们对真菌表型、抗病毒防御反应、病毒RNA重组活性和转座子表达的影响。无论是单个还是多个rdr敲除株,在有无病毒感染的情况下,与亲本菌株相比均未表现出任何表型差异,病毒RNA积累、重组活性或转座子RNA积累也无任何显著变化,这表明栗疫病菌的rdr基因对这些过程没有可检测到的贡献。