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A cell atlas of adult muscle precursors uncovers early events in fibre‐type divergence in Drosophila
In Drosophila, the wing disc‐associated muscle precursor cells give rise to the fibrillar indirect flight muscles (IFM) and the tubular direct flight muscles (DFM). To understand early transcriptional events underlying this muscle diversification, we performed single‐cell RNA‐sequencing experiments...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534622/ https://www.ncbi.nlm.nih.gov/pubmed/32815271 http://dx.doi.org/10.15252/embr.201949555 |
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author | Zappia, Maria Paula de Castro, Lucia Ariss, Majd M Jefferson, Holly Islam, Abul BMMK Frolov, Maxim V |
author_facet | Zappia, Maria Paula de Castro, Lucia Ariss, Majd M Jefferson, Holly Islam, Abul BMMK Frolov, Maxim V |
author_sort | Zappia, Maria Paula |
collection | PubMed |
description | In Drosophila, the wing disc‐associated muscle precursor cells give rise to the fibrillar indirect flight muscles (IFM) and the tubular direct flight muscles (DFM). To understand early transcriptional events underlying this muscle diversification, we performed single‐cell RNA‐sequencing experiments and built a cell atlas of myoblasts associated with third instar larval wing disc. Our analysis identified distinct transcriptional signatures for IFM and DFM myoblasts that underlie the molecular basis of their divergence. The atlas further revealed various states of differentiation of myoblasts, thus illustrating previously unappreciated spatial and temporal heterogeneity among them. We identified and validated novel markers for both IFM and DFM myoblasts at various states of differentiation by immunofluorescence and genetic cell‐tracing experiments. Finally, we performed a systematic genetic screen using a panel of markers from the reference cell atlas as an entry point and found a novel gene, Amalgam which is functionally important in muscle development. Our work provides a framework for leveraging scRNA‐seq for gene discovery and details a strategy that can be applied to other scRNA‐seq datasets. |
format | Online Article Text |
id | pubmed-7534622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75346222020-10-07 A cell atlas of adult muscle precursors uncovers early events in fibre‐type divergence in Drosophila Zappia, Maria Paula de Castro, Lucia Ariss, Majd M Jefferson, Holly Islam, Abul BMMK Frolov, Maxim V EMBO Rep Articles In Drosophila, the wing disc‐associated muscle precursor cells give rise to the fibrillar indirect flight muscles (IFM) and the tubular direct flight muscles (DFM). To understand early transcriptional events underlying this muscle diversification, we performed single‐cell RNA‐sequencing experiments and built a cell atlas of myoblasts associated with third instar larval wing disc. Our analysis identified distinct transcriptional signatures for IFM and DFM myoblasts that underlie the molecular basis of their divergence. The atlas further revealed various states of differentiation of myoblasts, thus illustrating previously unappreciated spatial and temporal heterogeneity among them. We identified and validated novel markers for both IFM and DFM myoblasts at various states of differentiation by immunofluorescence and genetic cell‐tracing experiments. Finally, we performed a systematic genetic screen using a panel of markers from the reference cell atlas as an entry point and found a novel gene, Amalgam which is functionally important in muscle development. Our work provides a framework for leveraging scRNA‐seq for gene discovery and details a strategy that can be applied to other scRNA‐seq datasets. John Wiley and Sons Inc. 2020-08-19 2020-10-05 /pmc/articles/PMC7534622/ /pubmed/32815271 http://dx.doi.org/10.15252/embr.201949555 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the 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 Zappia, Maria Paula de Castro, Lucia Ariss, Majd M Jefferson, Holly Islam, Abul BMMK Frolov, Maxim V A cell atlas of adult muscle precursors uncovers early events in fibre‐type divergence in Drosophila |
title | A cell atlas of adult muscle precursors uncovers early events in fibre‐type divergence in Drosophila
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title_full | A cell atlas of adult muscle precursors uncovers early events in fibre‐type divergence in Drosophila
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title_fullStr | A cell atlas of adult muscle precursors uncovers early events in fibre‐type divergence in Drosophila
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title_full_unstemmed | A cell atlas of adult muscle precursors uncovers early events in fibre‐type divergence in Drosophila
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title_short | A cell atlas of adult muscle precursors uncovers early events in fibre‐type divergence in Drosophila
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title_sort | cell atlas of adult muscle precursors uncovers early events in fibre‐type divergence in drosophila |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534622/ https://www.ncbi.nlm.nih.gov/pubmed/32815271 http://dx.doi.org/10.15252/embr.201949555 |
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