Comparative aspects on the role of polypyrimidine tract-binding protein in internal initiation of hepatitis C virus and picornavirus RNAs

被引:5
|
作者
Nishimura, T. [1 ,5 ]
Saito, M. [1 ]
Takano, T. [1 ,2 ,3 ]
Nomoto, A. [4 ]
Kohara, M. [2 ]
Tsukiyama-Kohara, K. [1 ,2 ,3 ]
机构
[1] Kumamoto Univ, Fac Med & Pharmaceut Sci, Dept Expt Phylaxiol, Kumamoto 8608556, Japan
[2] Tokyo Metropolitan Inst Med Sci, Dept Microbiol & Cell Biol, Tokyo 1138613, Japan
[3] Univ Tokyo, Inst Med Sci, Lab Anim Res Ctr, Tokyo 1088639, Japan
[4] Univ Tokyo, Grad Sch Med, Tokyo 1130033, Japan
[5] Chemoserotherapeut Res Inst, Tokyo 8691298, Japan
关键词
PTB; HCV; IRES; EMCV; PV; HeLa;
D O I
10.1016/j.cimid.2007.07.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We compared the effects of polypyrimidine tract-binding protein (PTB) on hepatitis C virus (HCV genotype IIa), encephalomyocarditis virus (EMCV) and poliovirus internal ribosome entry site (IRES) activities in vitro. It bound strongly to EMCV IRES, but weakly to PV and HCV RNAs. PV IRES showed the strongest dependency to PTB and it showed less than one-tenth of IRES activity after the immuno-depletion of PTB from HeLa S10 lysate with pre-coated anti-PTB IgG beads, comparing to the normal IgG beads-treated S10 lysate. EMCV IRES activity was approximately 40% of that of normal control after PTB depletion. Especially, HCV IRES activity was approximately 95%, and most weekly affected by the depletion of PTB. Repletion of PTB to depleted SIO lysate restored activities of PV and EMCV IRESs. The data suggest that PTB plays an important role in picornaviral IRESs, but not in HCV IRES. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:435 / 448
页数:14
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