首页> 美国卫生研究院文献>Frontiers in Microbiology >Promotion of Bamboo Mosaic Virus Accumulation in Nicotiana benthamiana by 5′→3′ Exonuclease NbXRN4
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Promotion of Bamboo Mosaic Virus Accumulation in Nicotiana benthamiana by 5′→3′ Exonuclease NbXRN4

机译:5'→3'核酸外切酶NbXRN4促进本生烟草中竹花叶病毒的积累

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摘要

Bamboo mosaic virus (BaMV) has a 6.4-kb (+) sense RNA genome with a 5′ cap and a 3′ poly(A) tail. ORF1 of this potexvirus encodes a 155-kDa replication protein responsible for the viral RNA replication/transcription and 5′ cap formation. To learn more about the replication complex of BaMV, a protein preparation enriched in the 155-kDa replication protein was obtained from Nicotiana benthamiana by a protocol involving agroinfiltration and immunoprecipitation. Subsequent analysis by SDS-PAGE and mass spectrometry identified a handful of host proteins that may participate in the viral replication. Among them, the cytoplasmic exoribonuclease NbXRN4 particularly caught our attention. NbXRN4 has been shown to have an antiviral activity against Tomato bushy stunt virus and Tomato mosaic virus. In Arabidopsis, the enzyme could reduce RNAi- and miRNA-mediated RNA decay. This study found that downregulation of NbXRN4 greatly decreased BaMV accumulation, while overexpression of NbXRN4 resulted in an opposite effect. Mutations at the catalytically essential residues abolished the function of NbXRN4 in the increase of BaMV accumulation. Nonetheless, NbXRN4 was still able to promote BaMV accumulation in the presence of the RNA silencing suppressor P19. In summary, the replication efficiency of BaMV may be improved by the exoribonuclease activity of NbXRN4.
机译:竹花叶病毒(BaMV)具有6.4-kb(+)有义RNA基因组,带有5'帽和3'poly(A)尾巴。该potexvirus的ORF1编码一个155 kDa的复制蛋白,负责病毒RNA复制/转录和5'帽的形成。为了更多地了解BaMV的复制复合物,通过涉及农业浸润和免疫沉淀的方案从本氏烟草中获得了富含155-kDa复制蛋白的蛋白质制品。随后通过SDS-PAGE和质谱分析,确定了少数可能参与病毒复制的宿主蛋白。其中,胞质外切核糖核酸酶NbXRN4特别引起我们的注意。 NbXRN4已显示对番茄浓密的特技病毒和番茄花叶病毒具有抗病毒活性。在拟南芥中,该酶可以减少RNAi和miRNA介导的RNA衰变。这项研究发现,NbXRN4的下调大大降低了BaMV的积累,而NbXRN4的过表达导致相反的作用。催化必需残基处的突变消除了BaMV积累增加中NbXRN4的功能。尽管如此,在RNA沉默抑制剂P19存在的情况下,NbXRN4仍然能够促进BaMV积累。总之,可以通过NbXRN4的核糖核酸外切酶活性来提高BaMV的复制效率。

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