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Alternative TSSs are co‐regulated in single cells in the mouse brain

Alternative transcription start sites (TSSs) have been extensively studied genome‐wide for many cell types and have been shown to be important during development and to regulate transcript abundance between cell types. Likewise, single‐cell gene expression has been extensively studied for many cell...

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Autores principales: Karlsson, Kasper, Lönnerberg, Peter, Linnarsson, Sten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448164/
https://www.ncbi.nlm.nih.gov/pubmed/28495919
http://dx.doi.org/10.15252/msb.20167374
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author Karlsson, Kasper
Lönnerberg, Peter
Linnarsson, Sten
author_facet Karlsson, Kasper
Lönnerberg, Peter
Linnarsson, Sten
author_sort Karlsson, Kasper
collection PubMed
description Alternative transcription start sites (TSSs) have been extensively studied genome‐wide for many cell types and have been shown to be important during development and to regulate transcript abundance between cell types. Likewise, single‐cell gene expression has been extensively studied for many cell types. However, how single cells use TSSs has not yet been examined. In particular, it is unknown whether alternative TSSs are independently expressed, or whether they are co‐activated or even mutually exclusive in single cells. Here, we use a previously published single‐cell RNA‐seq dataset, comprising thousands of cells, to study alternative TSS usage. We find that alternative TSS usage is a regulated process, and the correlation between two TSSs expressed in single cells of the same cell type is surprisingly high. Our findings indicate that TSSs generally are regulated by common factors rather than being independently regulated or stochastically expressed.
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spelling pubmed-54481642017-05-30 Alternative TSSs are co‐regulated in single cells in the mouse brain Karlsson, Kasper Lönnerberg, Peter Linnarsson, Sten Mol Syst Biol Articles Alternative transcription start sites (TSSs) have been extensively studied genome‐wide for many cell types and have been shown to be important during development and to regulate transcript abundance between cell types. Likewise, single‐cell gene expression has been extensively studied for many cell types. However, how single cells use TSSs has not yet been examined. In particular, it is unknown whether alternative TSSs are independently expressed, or whether they are co‐activated or even mutually exclusive in single cells. Here, we use a previously published single‐cell RNA‐seq dataset, comprising thousands of cells, to study alternative TSS usage. We find that alternative TSS usage is a regulated process, and the correlation between two TSSs expressed in single cells of the same cell type is surprisingly high. Our findings indicate that TSSs generally are regulated by common factors rather than being independently regulated or stochastically expressed. John Wiley and Sons Inc. 2017-05-11 /pmc/articles/PMC5448164/ /pubmed/28495919 http://dx.doi.org/10.15252/msb.20167374 Text en © 2017 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Karlsson, Kasper
Lönnerberg, Peter
Linnarsson, Sten
Alternative TSSs are co‐regulated in single cells in the mouse brain
title Alternative TSSs are co‐regulated in single cells in the mouse brain
title_full Alternative TSSs are co‐regulated in single cells in the mouse brain
title_fullStr Alternative TSSs are co‐regulated in single cells in the mouse brain
title_full_unstemmed Alternative TSSs are co‐regulated in single cells in the mouse brain
title_short Alternative TSSs are co‐regulated in single cells in the mouse brain
title_sort alternative tsss are co‐regulated in single cells in the mouse brain
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448164/
https://www.ncbi.nlm.nih.gov/pubmed/28495919
http://dx.doi.org/10.15252/msb.20167374
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