Poly(A)-tail profiling reveals an embryonic switch in translational control

Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths have impeded greater understanding of poly(A)-tail function. Here we describe poly(A)-tail length profiling by sequencing (PAL-seq) and apply it to measu...

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Main Authors: Subtelny, Alexander Orest, Eichhorn, Stephen William, Chen, Grace, Sive, Hazel L., Bartel, David
Other Authors: Harvard University--MIT Division of Health Sciences and Technology
Format: Article
Language:en_US
Published: Nature Publishing Group 2015
Online Access:http://hdl.handle.net/1721.1/96227
https://orcid.org/0000-0002-6410-4699
https://orcid.org/0000-0002-3872-2856
https://orcid.org/0000-0002-4890-424X
https://orcid.org/0000-0001-5029-5909
https://orcid.org/0000-0001-9051-1696
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author Subtelny, Alexander Orest
Eichhorn, Stephen William
Chen, Grace
Sive, Hazel L.
Bartel, David
author2 Harvard University--MIT Division of Health Sciences and Technology
author_facet Harvard University--MIT Division of Health Sciences and Technology
Subtelny, Alexander Orest
Eichhorn, Stephen William
Chen, Grace
Sive, Hazel L.
Bartel, David
author_sort Subtelny, Alexander Orest
collection MIT
description Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths have impeded greater understanding of poly(A)-tail function. Here we describe poly(A)-tail length profiling by sequencing (PAL-seq) and apply it to measure tail lengths of millions of individual RNAs isolated from yeasts, cell lines, Arabidopsis thaliana leaves, mouse liver, and zebrafish and frog embryos. Poly(A)-tail lengths were conserved between orthologous mRNAs, with mRNAs encoding ribosomal proteins and other ‘housekeeping’ proteins tending to have shorter tails. As expected, tail lengths were coupled to translational efficiencies in early zebrafish and frog embryos. However, this strong coupling diminished at gastrulation and was absent in non-embryonic samples, indicating a rapid developmental switch in the nature of translational control. This switch complements an earlier switch to zygotic transcriptional control and explains why the predominant effect of microRNA-mediated deadenylation concurrently shifts from translational repression to mRNA destabilization.
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spelling mit-1721.1/962272022-10-01T05:47:45Z Poly(A)-tail profiling reveals an embryonic switch in translational control Subtelny, Alexander Orest Eichhorn, Stephen William Chen, Grace Sive, Hazel L. Bartel, David Harvard University--MIT Division of Health Sciences and Technology Massachusetts Institute of Technology. Department of Biology Subtelny, Alexander Orest Eichhorn, Stephen William Chen, Grace Sive, Hazel L. Bartel, David Poly(A) tails enhance the stability and translation of most eukaryotic messenger RNAs, but difficulties in globally measuring poly(A)-tail lengths have impeded greater understanding of poly(A)-tail function. Here we describe poly(A)-tail length profiling by sequencing (PAL-seq) and apply it to measure tail lengths of millions of individual RNAs isolated from yeasts, cell lines, Arabidopsis thaliana leaves, mouse liver, and zebrafish and frog embryos. Poly(A)-tail lengths were conserved between orthologous mRNAs, with mRNAs encoding ribosomal proteins and other ‘housekeeping’ proteins tending to have shorter tails. As expected, tail lengths were coupled to translational efficiencies in early zebrafish and frog embryos. However, this strong coupling diminished at gastrulation and was absent in non-embryonic samples, indicating a rapid developmental switch in the nature of translational control. This switch complements an earlier switch to zygotic transcriptional control and explains why the predominant effect of microRNA-mediated deadenylation concurrently shifts from translational repression to mRNA destabilization. National Institutes of Health (U.S.) (Grant GM067031) National Institutes of Health (U.S.) (Medical Scientist Training Program Fellowship T32GM007753) 2015-03-27T18:08:51Z 2015-03-27T18:08:51Z 2014-01 2013-07 Article http://purl.org/eprint/type/JournalArticle 0028-0836 1476-4687 http://hdl.handle.net/1721.1/96227 Subtelny, Alexander O., Stephen W. Eichhorn, Grace R. Chen, Hazel Sive, and David P. Bartel. “Poly(A)-Tail Profiling Reveals an Embryonic Switch in Translational Control.” Nature 508, no. 7494 (January 29, 2014): 66–71. https://orcid.org/0000-0002-6410-4699 https://orcid.org/0000-0002-3872-2856 https://orcid.org/0000-0002-4890-424X https://orcid.org/0000-0001-5029-5909 https://orcid.org/0000-0001-9051-1696 en_US http://dx.doi.org/10.1038/nature13007 Nature Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. application/pdf Nature Publishing Group PMC
spellingShingle Subtelny, Alexander Orest
Eichhorn, Stephen William
Chen, Grace
Sive, Hazel L.
Bartel, David
Poly(A)-tail profiling reveals an embryonic switch in translational control
title Poly(A)-tail profiling reveals an embryonic switch in translational control
title_full Poly(A)-tail profiling reveals an embryonic switch in translational control
title_fullStr Poly(A)-tail profiling reveals an embryonic switch in translational control
title_full_unstemmed Poly(A)-tail profiling reveals an embryonic switch in translational control
title_short Poly(A)-tail profiling reveals an embryonic switch in translational control
title_sort poly a tail profiling reveals an embryonic switch in translational control
url http://hdl.handle.net/1721.1/96227
https://orcid.org/0000-0002-6410-4699
https://orcid.org/0000-0002-3872-2856
https://orcid.org/0000-0002-4890-424X
https://orcid.org/0000-0001-5029-5909
https://orcid.org/0000-0001-9051-1696
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