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Capturing hidden regulation based on noise change of gene expression level from single cell RNA-seq in yeast

Recent progress in high throughput single cell RNA-seq (scRNA-seq) has activated the development of data-driven inferring methods of gene regulatory networks. Most network estimations assume that perturbations produce downstream effects. However, the effects of gene perturbations are sometimes compe...

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Autores principales: Itoh, Thoma, Makino, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604932/
https://www.ncbi.nlm.nih.gov/pubmed/34799619
http://dx.doi.org/10.1038/s41598-021-01558-y
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author Itoh, Thoma
Makino, Takashi
author_facet Itoh, Thoma
Makino, Takashi
author_sort Itoh, Thoma
collection PubMed
description Recent progress in high throughput single cell RNA-seq (scRNA-seq) has activated the development of data-driven inferring methods of gene regulatory networks. Most network estimations assume that perturbations produce downstream effects. However, the effects of gene perturbations are sometimes compensated by a gene with redundant functionality (functional compensation). In order to avoid functional compensation, previous studies constructed double gene deletions, but its vast nature of gene combinations was not suitable for comprehensive network estimation. We hypothesized that functional compensation may emerge as a noise change without mean change (noise-only change) due to varying physical properties and strong compensation effects. Here, we show compensated interactions, which are not detected by mean change, are captured by noise-only change quantified from scRNA-seq. We investigated whether noise-only change genes caused by a single deletion of STP1 and STP2, which have strong functional compensation, are enriched in redundantly regulated genes. As a result, noise-only change genes are enriched in their redundantly regulated genes. Furthermore, novel downstream genes detected from noise change are enriched in “transport”, which is related to known downstream genes. Herein, we suggest the noise difference comparison has the potential to be applied as a new strategy for network estimation that capture even compensated interaction.
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spelling pubmed-86049322021-11-22 Capturing hidden regulation based on noise change of gene expression level from single cell RNA-seq in yeast Itoh, Thoma Makino, Takashi Sci Rep Article Recent progress in high throughput single cell RNA-seq (scRNA-seq) has activated the development of data-driven inferring methods of gene regulatory networks. Most network estimations assume that perturbations produce downstream effects. However, the effects of gene perturbations are sometimes compensated by a gene with redundant functionality (functional compensation). In order to avoid functional compensation, previous studies constructed double gene deletions, but its vast nature of gene combinations was not suitable for comprehensive network estimation. We hypothesized that functional compensation may emerge as a noise change without mean change (noise-only change) due to varying physical properties and strong compensation effects. Here, we show compensated interactions, which are not detected by mean change, are captured by noise-only change quantified from scRNA-seq. We investigated whether noise-only change genes caused by a single deletion of STP1 and STP2, which have strong functional compensation, are enriched in redundantly regulated genes. As a result, noise-only change genes are enriched in their redundantly regulated genes. Furthermore, novel downstream genes detected from noise change are enriched in “transport”, which is related to known downstream genes. Herein, we suggest the noise difference comparison has the potential to be applied as a new strategy for network estimation that capture even compensated interaction. Nature Publishing Group UK 2021-11-19 /pmc/articles/PMC8604932/ /pubmed/34799619 http://dx.doi.org/10.1038/s41598-021-01558-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Itoh, Thoma
Makino, Takashi
Capturing hidden regulation based on noise change of gene expression level from single cell RNA-seq in yeast
title Capturing hidden regulation based on noise change of gene expression level from single cell RNA-seq in yeast
title_full Capturing hidden regulation based on noise change of gene expression level from single cell RNA-seq in yeast
title_fullStr Capturing hidden regulation based on noise change of gene expression level from single cell RNA-seq in yeast
title_full_unstemmed Capturing hidden regulation based on noise change of gene expression level from single cell RNA-seq in yeast
title_short Capturing hidden regulation based on noise change of gene expression level from single cell RNA-seq in yeast
title_sort capturing hidden regulation based on noise change of gene expression level from single cell rna-seq in yeast
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604932/
https://www.ncbi.nlm.nih.gov/pubmed/34799619
http://dx.doi.org/10.1038/s41598-021-01558-y
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