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宿主Pex19p在番茄丛矮病毒复制蛋白的过氧化物酶体定位中发挥作用。

The host Pex19p plays a role in peroxisomal localization of tombusvirus replication proteins.

作者信息

Pathak Kunj B, Sasvari Zsuzsanna, Nagy Peter D

机构信息

Department of Plant Pathology, University of Kentucky, Lexington, KY 40546, USA.

出版信息

Virology. 2008 Sep 30;379(2):294-305. doi: 10.1016/j.virol.2008.06.044. Epub 2008 Aug 5.

DOI:10.1016/j.virol.2008.06.044
PMID:18684480
Abstract

Replication of Tomato bushy stunt virus (TBSV) RNA takes place on the cytosolic membrane surface of peroxisomes in plants and in yeast, a model host. To identify the host proteins involved in assisting the peroxisomal localization of the tombusvirus p33 replication protein, we tested if p33 could bind directly to yeast proteins involved in peroxisomal transport in vitro. This work has led to the demonstration of Pex19p-p33 interaction via pull-down and co-purification experiments. Pex19p was also detected in the tombusvirus replicase after protein cross-linking, suggesting that Pex19p transiently binds to the replicase as could be expected from a transporter. To validate the importance of Pex19p-p33 interaction in TBSV replication in yeast, we re-targeted Pex19p to the mitochondria, which resulted in the re-distribution of a large fraction of p33 to the mitochondria. The expression of the mitochondrial-targeted Pex19p inhibited TBSV RNA accumulation by 2-4-fold in vivo and reduced the in vitro activity of the tombusvirus replicase by 80%. These data support the model that Pex19p is a cellular transporter for localization of p33 replication protein to the host peroxisomal membranes.

摘要

番茄丛矮病毒(TBSV)RNA的复制发生在植物和作为模式宿主的酵母中过氧化物酶体的胞质膜表面。为了鉴定参与协助番茄病毒p33复制蛋白定位于过氧化物酶体的宿主蛋白,我们在体外测试了p33是否能直接与参与过氧化物酶体运输的酵母蛋白结合。这项工作通过下拉和共纯化实验证明了Pex19p与p33的相互作用。在蛋白质交联后,在番茄病毒复制酶中也检测到了Pex19p,这表明Pex19p如转运蛋白所预期的那样与复制酶短暂结合。为了验证Pex19p与p33的相互作用在酵母中TBSV复制中的重要性,我们将Pex19p重新靶向到线粒体,这导致大部分p33重新分布到线粒体。线粒体靶向的Pex19p的表达在体内抑制TBSV RNA积累2至4倍,并使番茄病毒复制酶的体外活性降低80%。这些数据支持了Pex19p是一种将p33复制蛋白定位于宿主过氧化物酶体膜的细胞转运蛋白的模型。

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