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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...

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Detalles Bibliográficos
Autores principales: Naik, Hemant Chandru, Hari, Kishore, Chandel, Deepshikha, Mandal, Susmita, Jolly, Mohit Kumar, Gayen, Srimonta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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.
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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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