Severe acute respiratory syndrome coronavirus protein 7a interacts with hSGT

被引:33
|
作者
Fielding, BC
Gunalan, V
Tan, THP
Chou, CF
Shen, S
Khan, S
Lim, SG
Hong, W
Tan, YJ
机构
[1] Inst Mol & Cell Biol, Collaborat Anti Viral Res Grp, Singapore 138673, Singapore
[2] Univ Western Cape, Dept Med Biosci, ZA-7535 Bellville, South Africa
关键词
SARS-CoV; ORF; 7a; SGT; TPR; protein-protein interaction; accessory protein;
D O I
10.1016/j.bbrc.2006.03.091
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Severe acute respiratory syndrome coronavirus (SARS-CoV) 7a is an accessory protein with no known homologues. In this study, we report the interaction of a SARS-CoV 7a and small glutamine-rich tetratricopeptide repeat-containing protein (SGT). SARS-CoV 7a and human SGT interaction was identified using a two-hybrid system screen and confirmed with interaction screens in cell culture and cellular co-localization studies. The SGT domain of interaction was mapped by deletion mutant analysis and results indicated that tetratricopeptide repeat 2 (aa 125-158) was essential for interaction. We also showed that 7a interacted with SARS-CoV structural proteins M (membrane) and E (envelope), which have been shown to be essential for virus-like particle formation. Taken together, our results coupled with data from studies of the interaction between SGT and HIV-1 vpu indicated that SGT could be involved in the life-cycle, possibly assembly of SARS-CoV. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1201 / 1208
页数:8
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