Translational enhancing activity in 5′ UTR of peste des petits ruminants virus fusion gene

被引:13
|
作者
Chulakasian, Songkhla [1 ]
Chang, Tien-Jye [1 ]
Tsai, Ching-Hsiu [2 ]
Wong, Min-Liang [1 ]
Hsu, Wei-Li [3 ]
机构
[1] Natl Chung Hsing Univ, Dept Vet Med, Coll Vet Med, Taichung 402, Taiwan
[2] Natl Chung Hsing Univ, Grad Inst Biotechnol, Taichung 402, Taiwan
[3] Natl Chung Hsing Univ, Grad Inst Microbiol & Publ Hlth, Coll Vet Med, Taichung 402, Taiwan
关键词
5; UTR; fusion gene; mRNA stability; peste des petits ruminants virus; translational enhancer; LONG UNTRANSLATED REGION; CANINE-DISTEMPER VIRUS; 18S RIBOSOMAL-RNA; MESSENGER-RNA; INITIATION; EXPRESSION; SEQUENCE; MORBILLIVIRUSES; REPLICATION; EFFICIENCY;
D O I
10.1111/febs.12115
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 fusion gene of peste des petits ruminants virus (PPRV-F), a paramyxovirus, contains an unusual long 5 untranslated region (5 UTR) with a high GC content that is capable of folding into secondary structure proximally to the 5 cap. Sequence analysis further suggested that the proximal end of this UTR contains a nine-nucleotide sequence which could perfectly complement the 18S rRNA and might affect translation through mRNArRNA interaction. Based on these features, we examined the functional role of the proximal PPRV-F 5 UTR on translational efficiency compared with two other morbilliviruses. From reporter gene assays, PPRV-F 5 UTR functioned as a strong enhancer of translational efficiency independent of cell and gene specificity. Northern blot analysis of the accumulative RNA levels and mRNA stability suggested that elevated gene expression driven by PPRV-F 5 UTR was accompanied by an increased mRNA level and enhanced mRNA stability. Deletion analysis identified the complementary sequence and distal nucleotides necessary for the enhancing activity, and results suggest RNA structural conformation is important. Taken together, we conclude that the proximal PPRV-F 5 UTR functions as a translational enhancer by promoting translation efficiency and mRNA stability.
引用
收藏
页码:1237 / 1248
页数:12
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