An RNA biosensor for imaging the first round of translation from single cells to living animals

Author:

Halstead James M.1,Lionnet Timothée234,Wilbertz Johannes H.15,Wippich Frank6,Ephrussi Anne6,Singer Robert H.234,Chao Jeffrey A.12

Affiliation:

1. Friedrich Miescher Institute for Biomedical Research, CH-4058 Basel, Switzerland.

2. Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

3. Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

4. Transcription Imaging Consortium, Howard Hughes Medical Institute Janelia Farm Research Campus, Ashburn, VA 20147, USA.

5. University of Basel, CH-4003 Basel, Switzerland.

6. Developmental Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.

Abstract

Measuring translation in space and time The ribosome translates the information contained within messenger RNAs (mRNAs) into proteins. When and where ribosomes encounter mRNAs can regulate gene expression. Halstead et al. developed an RNA biosensor that allows single molecules of mRNAs that have never been translated to be distinguished from ones that have undergone translation by the ribosome in living cells (see the Perspective by Popp and Maquat). The authors demonstrated the utility of their technique by examining the spatial and temporal regulation of translation in single cells and in Drosophila oocytes during development. Science , this issue p. 1367 ; see also p. 1316

Funder

NIH

Howard Hughes Medical Institute

Novartis Research Foundation

European Molecular Biology Laboratory

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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