共 33 条
hnRNP L is required for the translation mediated by HCV IRES
被引:49
作者:
Hwang, Byounghoon
[1
]
Lim, Jong Hoon
[1
]
Hahm, Bumsuk
[2
]
Jang, Sung Key
[2
]
Lee, Seong-Wook
[1
]
机构:
[1] Dankook Univ, Inst Nanosensor & Biotechnol, Dept Mol Biol, Yongin 448701, South Korea
[2] Pohang Univ Sci & Technol, Dept Life Sci, Kyungbuk 790784, South Korea
关键词:
HCV;
IRES;
hnRNP L;
Translation;
RNA aptamer;
HEPATITIS-C VIRUS;
INTERNAL RIBOSOME ENTRY;
TRACT-BINDING-PROTEIN;
5 NONCODING REGION;
FUNCTIONAL REQUIREMENT;
RNA STABILITY;
INITIATION;
SITE;
GENE;
SELECTION;
D O I:
10.1016/j.bbrc.2008.11.091
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:
Translation of hepatitis C virus (HCV) RNA is initiated by internal loading of the ribosome into the HCV internal ribosome entry site (IRES). Previously. heterogeneous ribonucleoprotein L (hnRNP L) was shown to bind specifically to the 3' border region of the HCV IRES and enhance HCV mRNA translation. Here, we provide evidence for the functional requirement of hnRNP L for the HCV IRES-mediated translation initiation using specific RNA aptamers. In vitro selection techniques were employed to isolate RNA aptamers against hnRNP L, which were shown to contain consensus sequences with repetitive ACAC/U. The hnRNP L-specific RNA aptamers efficiently inhibited the in vitro translation reactions mediated by the HCV IRES in rabbit reticulocyte lysates. RNA ligands with only (ACAU)5 or (AC)10 nucleotide sequences could also specifically bind to hnRNP L, and specifically and effectively impeded in vitro translation reactions controlled by the HCV [RES. Importantly, the hnRNP L-specific RNA aptamers inhibited the HCV IRES function in cells in a dose-dependent manner, and the aptamer-mediated inhibition of the HCV [RES was considerably relieved by the addition of hnRNP L-expressing vector. These results strongly demonstrate the functional requirement of cellular hnRNP L for the HCV IRES activity. (C) 2008 Elsevier Inc. All rights reserved.
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页码:584 / 588
页数:5
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