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Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation

Measuring multiple omics profiles from the same single cell opens up the opportunity to decode molecular regulation that underlies intercellular heterogeneity in development and disease. Here, we present co-sequencing of microRNAs and mRNAs in the same single cell using a half-cell genomics approach...

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Autores principales: Wang, Nayi, Zheng, Ji, Chen, Zhuo, Liu, Yang, Dura, Burak, Kwak, Minsuk, Xavier-Ferrucio, Juliana, Lu, Yi-Chien, Zhang, Miaomiao, Roden, Christine, Cheng, Jijun, Krause, Diane S., Ding, Ye, Fan, Rong, Lu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327095/
https://www.ncbi.nlm.nih.gov/pubmed/30626865
http://dx.doi.org/10.1038/s41467-018-07981-6
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author Wang, Nayi
Zheng, Ji
Chen, Zhuo
Liu, Yang
Dura, Burak
Kwak, Minsuk
Xavier-Ferrucio, Juliana
Lu, Yi-Chien
Zhang, Miaomiao
Roden, Christine
Cheng, Jijun
Krause, Diane S.
Ding, Ye
Fan, Rong
Lu, Jun
author_facet Wang, Nayi
Zheng, Ji
Chen, Zhuo
Liu, Yang
Dura, Burak
Kwak, Minsuk
Xavier-Ferrucio, Juliana
Lu, Yi-Chien
Zhang, Miaomiao
Roden, Christine
Cheng, Jijun
Krause, Diane S.
Ding, Ye
Fan, Rong
Lu, Jun
author_sort Wang, Nayi
collection PubMed
description Measuring multiple omics profiles from the same single cell opens up the opportunity to decode molecular regulation that underlies intercellular heterogeneity in development and disease. Here, we present co-sequencing of microRNAs and mRNAs in the same single cell using a half-cell genomics approach. This method demonstrates good robustness (~95% success rate) and reproducibility (R(2) = 0.93 for both microRNAs and mRNAs), yielding paired half-cell microRNA and mRNA profiles, which we can independently validate. By linking the level of microRNAs to the expression of predicted target mRNAs across 19 single cells that are phenotypically identical, we observe that the predicted targets are significantly anti-correlated with the variation of abundantly expressed microRNAs. This suggests that microRNA expression variability alone may lead to non-genetic cell-to-cell heterogeneity. Genome-scale analysis of paired microRNA-mRNA co-profiles further allows us to derive and validate regulatory relationships of cellular pathways controlling microRNA expression and intercellular variability.
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spelling pubmed-63270952019-03-28 Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation Wang, Nayi Zheng, Ji Chen, Zhuo Liu, Yang Dura, Burak Kwak, Minsuk Xavier-Ferrucio, Juliana Lu, Yi-Chien Zhang, Miaomiao Roden, Christine Cheng, Jijun Krause, Diane S. Ding, Ye Fan, Rong Lu, Jun Nat Commun Article Measuring multiple omics profiles from the same single cell opens up the opportunity to decode molecular regulation that underlies intercellular heterogeneity in development and disease. Here, we present co-sequencing of microRNAs and mRNAs in the same single cell using a half-cell genomics approach. This method demonstrates good robustness (~95% success rate) and reproducibility (R(2) = 0.93 for both microRNAs and mRNAs), yielding paired half-cell microRNA and mRNA profiles, which we can independently validate. By linking the level of microRNAs to the expression of predicted target mRNAs across 19 single cells that are phenotypically identical, we observe that the predicted targets are significantly anti-correlated with the variation of abundantly expressed microRNAs. This suggests that microRNA expression variability alone may lead to non-genetic cell-to-cell heterogeneity. Genome-scale analysis of paired microRNA-mRNA co-profiles further allows us to derive and validate regulatory relationships of cellular pathways controlling microRNA expression and intercellular variability. Nature Publishing Group UK 2019-01-09 /pmc/articles/PMC6327095/ /pubmed/30626865 http://dx.doi.org/10.1038/s41467-018-07981-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Nayi
Zheng, Ji
Chen, Zhuo
Liu, Yang
Dura, Burak
Kwak, Minsuk
Xavier-Ferrucio, Juliana
Lu, Yi-Chien
Zhang, Miaomiao
Roden, Christine
Cheng, Jijun
Krause, Diane S.
Ding, Ye
Fan, Rong
Lu, Jun
Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation
title Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation
title_full Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation
title_fullStr Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation
title_full_unstemmed Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation
title_short Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation
title_sort single-cell microrna-mrna co-sequencing reveals non-genetic heterogeneity and mechanisms of microrna regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327095/
https://www.ncbi.nlm.nih.gov/pubmed/30626865
http://dx.doi.org/10.1038/s41467-018-07981-6
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