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Differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types

Alternative polyadenylation (APA) regulates mRNA translation, stability, and protein localization. However, it is unclear to what extent APA regulates these processes uniquely in specific cell types. Using a new technique, cTag-PAPERCLIP, we discovered significant differences in APA between the prin...

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Autores principales: Jereb, Saša, Hwang, Hun-Way, Van Otterloo, Eric, Govek, Eve-Ellen, Fak, John J, Yuan, Yuan, Hatten, Mary E, Darnell, Robert B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898910/
https://www.ncbi.nlm.nih.gov/pubmed/29578408
http://dx.doi.org/10.7554/eLife.34042
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author Jereb, Saša
Hwang, Hun-Way
Van Otterloo, Eric
Govek, Eve-Ellen
Fak, John J
Yuan, Yuan
Hatten, Mary E
Darnell, Robert B
author_facet Jereb, Saša
Hwang, Hun-Way
Van Otterloo, Eric
Govek, Eve-Ellen
Fak, John J
Yuan, Yuan
Hatten, Mary E
Darnell, Robert B
author_sort Jereb, Saša
collection PubMed
description Alternative polyadenylation (APA) regulates mRNA translation, stability, and protein localization. However, it is unclear to what extent APA regulates these processes uniquely in specific cell types. Using a new technique, cTag-PAPERCLIP, we discovered significant differences in APA between the principal types of mouse cerebellar neurons, the Purkinje and granule cells, as well as between proliferating and differentiated granule cells. Transcripts that differed in APA in these comparisons were enriched in key neuronal functions and many differed in coding sequence in addition to 3’UTR length. We characterize Memo1, a transcript that shifted from expressing a short 3’UTR isoform to a longer one during granule cell differentiation. We show that Memo1 regulates granule cell precursor proliferation and that its long 3’UTR isoform is targeted by miR-124, contributing to its downregulation during development. Our findings provide insight into roles for APA in specific cell types and establish a platform for further functional studies.
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spelling pubmed-58989102018-04-16 Differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types Jereb, Saša Hwang, Hun-Way Van Otterloo, Eric Govek, Eve-Ellen Fak, John J Yuan, Yuan Hatten, Mary E Darnell, Robert B eLife Neuroscience Alternative polyadenylation (APA) regulates mRNA translation, stability, and protein localization. However, it is unclear to what extent APA regulates these processes uniquely in specific cell types. Using a new technique, cTag-PAPERCLIP, we discovered significant differences in APA between the principal types of mouse cerebellar neurons, the Purkinje and granule cells, as well as between proliferating and differentiated granule cells. Transcripts that differed in APA in these comparisons were enriched in key neuronal functions and many differed in coding sequence in addition to 3’UTR length. We characterize Memo1, a transcript that shifted from expressing a short 3’UTR isoform to a longer one during granule cell differentiation. We show that Memo1 regulates granule cell precursor proliferation and that its long 3’UTR isoform is targeted by miR-124, contributing to its downregulation during development. Our findings provide insight into roles for APA in specific cell types and establish a platform for further functional studies. eLife Sciences Publications, Ltd 2018-03-26 /pmc/articles/PMC5898910/ /pubmed/29578408 http://dx.doi.org/10.7554/eLife.34042 Text en © 2018, Jereb et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Jereb, Saša
Hwang, Hun-Way
Van Otterloo, Eric
Govek, Eve-Ellen
Fak, John J
Yuan, Yuan
Hatten, Mary E
Darnell, Robert B
Differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types
title Differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types
title_full Differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types
title_fullStr Differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types
title_full_unstemmed Differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types
title_short Differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types
title_sort differential 3’ processing of specific transcripts expands regulatory and protein diversity across neuronal cell types
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898910/
https://www.ncbi.nlm.nih.gov/pubmed/29578408
http://dx.doi.org/10.7554/eLife.34042
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