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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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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. |
format | Online Article Text |
id | pubmed-5898910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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