Ribosome profiling reveals resemblance between long non-coding RNAs and 5′ leaders of coding RNAs

被引:207
作者
Chew, Guo-Liang [1 ]
Pauli, Andrea [1 ]
Rinn, John L. [2 ,3 ]
Regev, Aviv [3 ,4 ]
Schier, Alexander F. [1 ,3 ,5 ]
Valen, Eivind [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[3] Broad Inst Massachusetts Inst Technol & Harvard, Cambridge, MA 02142 USA
[4] MIT, Dept Biol, Howard Hughes Med Inst, Cambridge, MA 02139 USA
[5] Harvard Univ, FAS Ctr Syst, Cambridge, MA 02138 USA
来源
DEVELOPMENT | 2013年 / 140卷 / 13期
基金
美国国家卫生研究院;
关键词
Long non-coding RNAs; Ribosome profiling; Embryogenesis; Zebrafish; ES cells; GENOME-WIDE ANALYSIS; OPEN READING FRAMES; EMBRYONIC-DEVELOPMENT; XIST GENE; IN-VIVO; TRANSLATION; IDENTIFICATION; ANNOTATION; EXPRESSION; LANDSCAPE;
D O I
10.1242/dev.098343
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Large-scale genomics and computational approaches have identified thousands of putative long non-coding RNAs (lncRNAs). It has been controversial, however, as to what fraction of these RNAs is truly non-coding. Here, we combine ribosome profiling with a machine-learning approach to validate lncRNAs during zebrafish development in a high throughput manner. We find that dozens of proposed lncRNAs are protein-coding contaminants and that many lncRNAs have ribosome profiles that resemble the 5' leaders of coding RNAs. Analysis of ribosome profiling data from embryonic stem cells reveals similar properties for mammalian lncRNAs. These results clarify the annotation of developmental lncRNAs and suggest a potential role for translation in lncRNA regulation. In addition, our computational pipeline and ribosome profiling data provide a powerful resource for the identification of translated open reading frames during zebrafish development.
引用
收藏
页码:2828 / 2834
页数:7
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