High frequency of+1 programmed ribosomal frameshifting in Euplotes octocarinatus

被引:38
|
作者
Wang, Ruanlin [1 ]
Xiong, Jie [2 ]
Wang, Wei [1 ]
Miao, Wei [2 ]
Liang, Aihua [1 ]
机构
[1] Shanxi Univ, Inst Biotechnol, Minist Educ, Key Lab Chem Biol & Mol Engn, Taiyuan 030006, Peoples R China
[2] Chinese Acad Sci, Inst Hydrobiol, Key Lab Aquat Biodivers & Conservat, Wuhan 430072, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
中国国家自然科学基金;
关键词
ORNITHINE-DECARBOXYLASE ANTIZYME; TRANSFER-RNA GENES; STRUCTURAL INSIGHTS; ANTICODON STEM; CRASSUS TEC1; PROTEIN; IDENTIFICATION; EXPRESSION; GENOME; MACRONUCLEAR;
D O I
10.1038/srep21139
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Programmed -1 ribosomal frameshifting (-1 PRF) has been identified as a mechanism to regulate the expression of many viral genes and some cellular genes. The slippery site of -1 PRF has been well characterized, whereas the + 1 PRF signal and the mechanism involved in + 1 PRF remain poorly understood. Previous study confirmed that + 1 PRF is required for the synthesis of protein products in several genes of ciliates from the genus Euplotes. To accurately assess the frequency of genes requiring frameshift in Euplotes, the macronuclear genome and transcriptome of Euplotes octocarinatus were analyzed in this study. A total of 3,700 + 1 PRF candidate genes were identified from 32,353 transcripts, and the gene products of these putative + 1 PRFs were mainly identified as protein kinases. Furthermore, we reported a putative suppressor tRNA of UAA which may provide new insights into the mechanism of + 1 PRF in euplotids. For the first time, our transcriptome-wide survey of + 1 PRF in E. octocarinatus provided a dataset which serves as a valuable resource for the future understanding of the mechanism underlying + 1 PRF.
引用
收藏
页数:12
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