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

Author:

Chew Guo-Liang1,Pauli Andrea1,Rinn John L.23,Regev Aviv34,Schier Alexander F.135,Valen Eivind1

Affiliation:

1. Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.

2. Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.

3. The Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, MA 02142, USA.

4. Howard Hughes Medical Institute, Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

5. FAS Center for Systems Biology, Harvard University, Cambridge, MA 02138, USA.

Abstract

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.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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