The Long Non-coding RNA lnc-31 Interacts with Rock1 mRNA and Mediates Its YB-1-Dependent Translation

被引:49
作者
Dimartino, Dacia [1 ]
Colantoni, Alessio [1 ]
Ballarino, Monica [1 ]
Martone, Julie [1 ]
Mariani, Davide [1 ]
Danner, Johannes [2 ]
Bruckmann, Astrid [2 ]
Meister, Gunter [2 ]
Morlando, Mariangela [1 ]
Bozzoni, Irene [1 ,3 ,4 ]
机构
[1] Sapienza Univ Rome, Dept Biol & Biotechnol, Ple A Moro 5, I-00185 Rome, Italy
[2] Univ Regensburg, Lab RNA Biol, Biochem Ctr Regensburg, D-93053 Regensburg, Germany
[3] Ist Italiano Tecnol, Ctr Life Nano Sci Sapienza, Viale Regina Elena 291, I-00161 Rome, Italy
[4] Sapienza Univ Rome, Inst Pasteur Fdn Cenci Bolognetti, Ple A Moro 5, I-00185 Rome, Italy
来源
CELL REPORTS | 2018年 / 23卷 / 03期
基金
欧洲研究理事会;
关键词
YB-1; PROMOTES; MYOGENIC DIFFERENTIATION; MUSCLE DIFFERENTIATION; SKELETAL-MUSCLE; MYOBLAST FUSION; NEURAL ACTIVITY; EXPRESSION; TRANSCRIPTION; LOCALIZATION; ACTIVATION;
D O I
10.1016/j.celrep.2018.03.101
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytoplasmic long non-coding RNAs have been shown to act at many different levels to control post-transcriptional gene expression, although their role in translational control is poorly understood. Here, we show that lnc-31, a non-coding RNA required for myoblast proliferation, promotes ROCK1 protein synthesis by stabilizing its translational activator, YB-1. We find that lnc-31 binds to the Rock1 mRNA as well as to the YB-1 protein and that translational activation requires physical interaction between the two RNA species. These results suggest a localized effect of YB-1 stabilization on the Rock1 mRNA. ROCK1 upregulation by lnc-31, in proliferative conditions, correlates well with the differentiation-repressing activity of ROCK1. We also show that, upon induction of differentiation, the downregulation of lnc-31, in conjunction with miR-152 targeting of Rock1, establishes a regulatory loop that reinforces ROCK1 repression and promotes myogenesis.
引用
收藏
页码:733 / 740
页数:8
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