Nuclear translation visualized by ribosome-bound nascent chain puromycylation

Author:

David Alexandre1,Dolan Brian P.1,Hickman Heather D.1,Knowlton Jonathan J.1,Clavarino Giovanna234,Pierre Philippe234,Bennink Jack R.1,Yewdell Jonathan W.1

Affiliation:

1. Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892

2. Centre d’Immunologie de Marseille-Luminy Aix-Marseille Université, 13288 Marseille, France

3. Institut National de la Santé et de la Recherche Médicale, U1104, 13288 Marseille, France

4. Centre National de la Recherche Scientifique, Unité Mixte de Recherche 7280, 13288 Marseille, France

Abstract

Whether protein translation occurs in the nucleus is contentious. To address this question, we developed the ribopuromycylation method (RPM), which visualizes translation in cells via standard immunofluorescence microscopy. The RPM is based on ribosome-catalyzed puromycylation of nascent chains immobilized on ribosomes by antibiotic chain elongation inhibitors followed by detection of puromycylated ribosome-bound nascent chains with a puromycin (PMY)-specific monoclonal antibody in fixed and permeabilized cells. The RPM correlates localized translation with myriad processes in cells and can be applied to any cell whose translation is sensitive to PMY. In this paper, we use the RPM to provide evidence for translation in the nucleoplasm and nucleolus, which is regulated by infectious and chemical stress.

Publisher

Rockefeller University Press

Subject

Cell Biology

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