Expression of a MORN repeat protein from Euplotes octocarinatus requires a+1 programmed ribosomal frameshifting

被引:0
|
作者
Wei, Lili [1 ]
Zhao, Xuemei [1 ]
Wang, Ruanlin [1 ]
Fu, Yuejun [1 ]
Chai, Baofeng [1 ]
Liang, Aihua [1 ]
机构
[1] Shanxi Univ, Inst Biotechnol, Key Lab Chem Biol & Mol Engn, Minist Educ, Taiyuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Euplotes octocarinatus; programmed ribosomal frameshifting; MORN; dual-luciferase experiment; mass spectrometry; GENE-EXPRESSION; MESSENGER-RNA; HIV-1; YEAST; TETRAHYMENA; EFFICIENCY; BACTERIAL; SLIPPAGE; SUPPORTS; HUMANS;
D O I
10.1080/09168451.2017.1301804
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
Analysis of transcriptome revealed that a membrane occupation and recognition nexus (MORN) repeat protein-encoding gene of Euplotes octocarinatus (Eo-morn-9-31) was a candidate for programmed +1 ribosomal frameshifting (+1 PRF). In this study, a dual-luciferase assay was performed to detect its expression. The result showed that the MORN repeat protein (Eo-MORN-9-31) could be produced by the +1 PRF event during the process of translation in yeast and the frameshifting efficiency was about 4-5%. We further confirmed its reality by western blot and mass spectrometry. This study provided experimental evidence indicating that the expression of the Eo-MORN-9-31 of E. octocarinatus required the +1 PRF.
引用
收藏
页码:1327 / 1334
页数:8
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