A peptide inhibitor of exportin1 blocks shuttling of the adenoviral E1B 55 kDa protein but not export of viral late mRNAs

被引:16
作者
Flint, SJ [1 ]
Huang, WY [1 ]
Goodhouse, J [1 ]
Kyin, S [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
基金
美国国家卫生研究院;
关键词
adenoviral E1B 55 kDa protein; mPNA export; exportin1; peptide inhibitor;
D O I
10.1016/j.virol.2005.04.007
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The human subgroup C adenoviral E1B55 kDa and E4 Orf6 proteins are required for efficient nuclear export of viral late mRNAs, but the cellular pathway that mediates such export has not been identified. As a first step to develop a general approach to address this issue, we have assessed the utility of cell-permeable peptide inhibitors of cellular export receptors. As both E1B and E4 proteins have been reported to containing a leucine-rich nuclear export signal (NES), we synthesized a cell-permeable peptide containing such an NES. This peptide induced substantial inhibition of export of the E1B protein, whereas a control, non-functional peptide did not. However, under the same conditions, the NES peptide had no effect on export of viral late mRNAs. These observations establish that viral late mRNAs are not exported by exportin1, as well as the value of peptide inhibitors in investigation of mRNA export regulation in adenovirus-infected cells. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:7 / 17
页数:11
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