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Semicoordinated allelic-bursting shape dynamic random monoallelic expression in pregastrulation embryos
Recently, allele-specific single-cell RNA-seq analysis has demonstrated widespread dynamic random monoallelic expression of autosomal genes (aRME) in different cell types. However, the prevalence of dynamic aRME during pregastrulation remains unknown. Here, we show that dynamic aRME is widespread in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379509/ https://www.ncbi.nlm.nih.gov/pubmed/34458702 http://dx.doi.org/10.1016/j.isci.2021.102954 |
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author | Naik, Hemant Chandru Hari, Kishore Chandel, Deepshikha Mandal, Susmita Jolly, Mohit Kumar Gayen, Srimonta |
author_facet | Naik, Hemant Chandru Hari, Kishore Chandel, Deepshikha Mandal, Susmita Jolly, Mohit Kumar Gayen, Srimonta |
author_sort | Naik, Hemant Chandru |
collection | PubMed |
description | Recently, allele-specific single-cell RNA-seq analysis has demonstrated widespread dynamic random monoallelic expression of autosomal genes (aRME) in different cell types. However, the prevalence of dynamic aRME during pregastrulation remains unknown. Here, we show that dynamic aRME is widespread in different lineages of pregastrulation embryos. Additionally, the origin of dynamic aRME remains elusive. It is believed that independent transcriptional bursting from each allele leads to dynamic aRME. Here, we show that allelic burst is not perfectly independent; instead it happens in a semicoordinated fashion. Importantly, we show that semicoordinated allelic bursting of genes, particularly with low burst frequency, leads to frequent asynchronous allelic bursting, thereby contributing to dynamic aRME. Furthermore, we found that coordination of allelic bursting is lineage specific and genes regulating the development have a higher degree of coordination. Altogether, our study provides significant insights into the prevalence and origin of dynamic aRME and their developmental relevance during early development. |
format | Online Article Text |
id | pubmed-8379509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83795092021-08-27 Semicoordinated allelic-bursting shape dynamic random monoallelic expression in pregastrulation embryos Naik, Hemant Chandru Hari, Kishore Chandel, Deepshikha Mandal, Susmita Jolly, Mohit Kumar Gayen, Srimonta iScience Article Recently, allele-specific single-cell RNA-seq analysis has demonstrated widespread dynamic random monoallelic expression of autosomal genes (aRME) in different cell types. However, the prevalence of dynamic aRME during pregastrulation remains unknown. Here, we show that dynamic aRME is widespread in different lineages of pregastrulation embryos. Additionally, the origin of dynamic aRME remains elusive. It is believed that independent transcriptional bursting from each allele leads to dynamic aRME. Here, we show that allelic burst is not perfectly independent; instead it happens in a semicoordinated fashion. Importantly, we show that semicoordinated allelic bursting of genes, particularly with low burst frequency, leads to frequent asynchronous allelic bursting, thereby contributing to dynamic aRME. Furthermore, we found that coordination of allelic bursting is lineage specific and genes regulating the development have a higher degree of coordination. Altogether, our study provides significant insights into the prevalence and origin of dynamic aRME and their developmental relevance during early development. Elsevier 2021-08-05 /pmc/articles/PMC8379509/ /pubmed/34458702 http://dx.doi.org/10.1016/j.isci.2021.102954 Text en © 2021 The Authors. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Naik, Hemant Chandru Hari, Kishore Chandel, Deepshikha Mandal, Susmita Jolly, Mohit Kumar Gayen, Srimonta Semicoordinated allelic-bursting shape dynamic random monoallelic expression in pregastrulation embryos |
title | Semicoordinated allelic-bursting shape dynamic random monoallelic expression in pregastrulation embryos |
title_full | Semicoordinated allelic-bursting shape dynamic random monoallelic expression in pregastrulation embryos |
title_fullStr | Semicoordinated allelic-bursting shape dynamic random monoallelic expression in pregastrulation embryos |
title_full_unstemmed | Semicoordinated allelic-bursting shape dynamic random monoallelic expression in pregastrulation embryos |
title_short | Semicoordinated allelic-bursting shape dynamic random monoallelic expression in pregastrulation embryos |
title_sort | semicoordinated allelic-bursting shape dynamic random monoallelic expression in pregastrulation embryos |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379509/ https://www.ncbi.nlm.nih.gov/pubmed/34458702 http://dx.doi.org/10.1016/j.isci.2021.102954 |
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