Literature DB >> 28798045

Global mRNA polarization regulates translation efficiency in the intestinal epithelium.

Andreas E Moor1, Matan Golan1, Efi E Massasa1, Doron Lemze1, Tomer Weizman1, Rom Shenhav1, Shaked Baydatch1, Orel Mizrahi2, Roni Winkler2, Ofra Golani3, Noam Stern-Ginossar2, Shalev Itzkovitz4.   

Abstract

Asymmetric messenger RNA (mRNA) localization facilitates efficient translation in cells such as neurons and fibroblasts. However, the extent and importance of mRNA polarization in epithelial tissues are unclear. Here, we used single-molecule transcript imaging and subcellular transcriptomics to uncover global apical-basal intracellular polarization of mRNA in the mouse intestinal epithelium. The localization of mRNAs did not generally overlap protein localization. Instead, ribosomes were more abundant on the apical sides, and apical transcripts were consequently more efficiently translated. Refeeding of fasted mice elicited a basal-to-apical shift in polarization of mRNAs encoding ribosomal proteins, which was associated with a specific boost in their translation. This led to increased protein production, required for efficient nutrient absorption. These findings reveal a posttranscriptional regulatory mechanism involving dynamic polarization of mRNA and polarized translation.
Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2017        PMID: 28798045      PMCID: PMC5955215          DOI: 10.1126/science.aan2399

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  51 in total

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7.  Genome-wide analysis in vivo of translation with nucleotide resolution using ribosome profiling.

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Review 2.  Ribosome Profiling: Global Views of Translation.

Authors:  Nicholas T Ingolia; Jeffrey A Hussmann; Jonathan S Weissman
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Review 3.  Translational Control during Developmental Transitions.

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Review 10.  Fluorescence Imaging Methods to Investigate Translation in Single Cells.

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