Minor contribution of an internal ribosome entry site in the 5'-UTR of ornithine decarboxylase mRNA on its translation

被引:4
|
作者
Nishimura, Kazuhiro
Sakuma, Al
Yamashita, Tomoko
Hirokawa, Go
Imataka, Hiroaki
Kashiwagi, Keiko
Igarashi, Kazuei [1 ]
机构
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Chuo Ku, Chiba 2608675, Japan
[2] RIKEN, Genom Sci Ctr, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[3] Chiba Inst Sci, Fac Pharm, Chiba 2880025, Japan
关键词
ODC synthesis; IRES; 5'-UTR of mRNA;
D O I
10.1016/j.bbrc.2007.09.112
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
The mechanism of synthesis of ornithine decarboxylase (ODC) at the level of translation was studied using cell culture and cell-free systems. Synthesis of firefly luciferase (Flue) from the second open reading frame (ORF) in a bicistronic construct transfected into FM3A and HeLa cells was enhanced by the presence of the 5'-untranslated region (5'-UTR) of ODC mRNA between the two ORFs. However, cotransfection of the gene encoding 2A protease inhibited the synthesis of Flue. Synthesis of Flue from the second cistron in the bicistronic mRNA in a cell-free system was not affected significantly by the 5'-UTR of ODC mRNA. Synthesis of ODC from ODC mRNA in a cell-free system was inhibited by 2A protease and cap analogue (M(7)GpppG). Rapamycin inhibited ODC synthesis by 40-50% at both the G(1)/S boundary and the G(2)/M phase. These results indicate that an IRES in the 5'-UTR of ODC mRNA does not function effectively. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:124 / 130
页数:7
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