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烟草原生质体谷胱甘肽转移酶 NbGSTU4 参与调控竹嵌纹病毒的早期复制。

The glutathione transferase of Nicotiana benthamiana NbGSTU4 plays a role in regulating the early replication of Bamboo mosaic virus.

机构信息

Graduate Institute of Biotechnology, National Chung Hsing University, Taichung, Taiwan.

出版信息

New Phytol. 2013 Aug;199(3):749-57. doi: 10.1111/nph.12304. Epub 2013 May 23.

Abstract

Bamboo mosaic virus (BaMV) is a single-stranded positive-sense RNA virus. One of the plant glutathione S-transferase (GST) genes, NbGSTU4, responds as an upregulated gene in Nicotiana benthamiana post BaMV infection. In order to identify the role of NbGSTU4 in BaMV infection, the expression of NbGSTU4 was knocked down using a virus-induced gene silencing technique or was transiently expressed in N. benthamiana in BaMV inoculation. The results show a significant decrease in BaMV RNA accumulation when the expression level of NbGSTU4 is reduced; whereas the viral RNA accumulation increases when NbGSTU4 is transiently expressed. Furthermore, this study identified that the involvement of NbGSTU4 in viral RNA accumulation occurs by its participation in the viral early replication step. The findings show that the NbGSTU4 protein expressed from Escherichia coli can interact with the 3' untranslated region (UTR) of the BaMV RNA in vitro in the presence of glutathione (GSH). The addition of GSH in the in vitro replication assay shows an enhancement of minus-strand but not plus-strand RNA synthesis. The results suggest that the plant GST protein plays a role in binding viral RNA and delivering GSH to the replication complex to create a reduced condition for BaMV minus-strand RNA synthesis.

摘要

竹嵌纹病毒(BaMV)是一种单链正链 RNA 病毒。植物谷胱甘肽 S-转移酶(GST)基因之一,NbGSTU4,在感染 BaMV 后作为上调基因在 Nicotiana benthamiana 中响应。为了确定 NbGSTU4 在 BaMV 感染中的作用,使用病毒诱导的基因沉默技术敲低 NbGSTU4 的表达,或在 BaMV 接种时在 N. benthamiana 中瞬时表达 NbGSTU4。结果表明,当 NbGSTU4 的表达水平降低时,BaMV RNA 积累显著减少;而当瞬时表达 NbGSTU4 时,病毒 RNA 积累增加。此外,本研究还确定了 NbGSTU4 参与病毒 RNA 积累是通过其参与病毒早期复制步骤。研究结果表明,从大肠杆菌中表达的 NbGSTU4 蛋白可以在谷胱甘肽(GSH)存在的情况下与 BaMV RNA 的 3'非翻译区(UTR)在体外相互作用。在体外复制测定中添加 GSH 可增强负链但不增强正链 RNA 的合成。结果表明,植物 GST 蛋白在结合病毒 RNA 和向复制复合物输送 GSH 以创造 BaMV 负链 RNA 合成的还原条件方面发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0c6/3744755/4052bb31914c/nph0199-0749-f1.jpg

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