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A transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle

Muscles organise pseudo-crystalline arrays of actin, myosin and titin filaments to build force-producing sarcomeres. To study sarcomerogenesis, we have generated a transcriptomics resource of developing Drosophila flight muscles and identified 40 distinct expression profile clusters. Strikingly, mos...

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Autores principales: Spletter, Maria L, Barz, Christiane, Yeroslaviz, Assa, Zhang, Xu, Lemke, Sandra B, Bonnard, Adrien, Brunner, Erich, Cardone, Giovanni, Basler, Konrad, Habermann, Bianca H, Schnorrer, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005683/
https://www.ncbi.nlm.nih.gov/pubmed/29846170
http://dx.doi.org/10.7554/eLife.34058
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author Spletter, Maria L
Barz, Christiane
Yeroslaviz, Assa
Zhang, Xu
Lemke, Sandra B
Bonnard, Adrien
Brunner, Erich
Cardone, Giovanni
Basler, Konrad
Habermann, Bianca H
Schnorrer, Frank
author_facet Spletter, Maria L
Barz, Christiane
Yeroslaviz, Assa
Zhang, Xu
Lemke, Sandra B
Bonnard, Adrien
Brunner, Erich
Cardone, Giovanni
Basler, Konrad
Habermann, Bianca H
Schnorrer, Frank
author_sort Spletter, Maria L
collection PubMed
description Muscles organise pseudo-crystalline arrays of actin, myosin and titin filaments to build force-producing sarcomeres. To study sarcomerogenesis, we have generated a transcriptomics resource of developing Drosophila flight muscles and identified 40 distinct expression profile clusters. Strikingly, most sarcomeric components group in two clusters, which are strongly induced after all myofibrils have been assembled, indicating a transcriptional transition during myofibrillogenesis. Following myofibril assembly, many short sarcomeres are added to each myofibril. Subsequently, all sarcomeres mature, reaching 1.5 µm diameter and 3.2 µm length and acquiring stretch-sensitivity. The efficient induction of the transcriptional transition during myofibrillogenesis, including the transcriptional boost of sarcomeric components, requires in part the transcriptional regulator Spalt major. As a consequence of Spalt knock-down, sarcomere maturation is defective and fibers fail to gain stretch-sensitivity. Together, this defines an ordered sarcomere morphogenesis process under precise transcriptional control – a concept that may also apply to vertebrate muscle or heart development.
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spelling pubmed-60056832018-06-20 A transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle Spletter, Maria L Barz, Christiane Yeroslaviz, Assa Zhang, Xu Lemke, Sandra B Bonnard, Adrien Brunner, Erich Cardone, Giovanni Basler, Konrad Habermann, Bianca H Schnorrer, Frank eLife Cell Biology Muscles organise pseudo-crystalline arrays of actin, myosin and titin filaments to build force-producing sarcomeres. To study sarcomerogenesis, we have generated a transcriptomics resource of developing Drosophila flight muscles and identified 40 distinct expression profile clusters. Strikingly, most sarcomeric components group in two clusters, which are strongly induced after all myofibrils have been assembled, indicating a transcriptional transition during myofibrillogenesis. Following myofibril assembly, many short sarcomeres are added to each myofibril. Subsequently, all sarcomeres mature, reaching 1.5 µm diameter and 3.2 µm length and acquiring stretch-sensitivity. The efficient induction of the transcriptional transition during myofibrillogenesis, including the transcriptional boost of sarcomeric components, requires in part the transcriptional regulator Spalt major. As a consequence of Spalt knock-down, sarcomere maturation is defective and fibers fail to gain stretch-sensitivity. Together, this defines an ordered sarcomere morphogenesis process under precise transcriptional control – a concept that may also apply to vertebrate muscle or heart development. eLife Sciences Publications, Ltd 2018-05-30 /pmc/articles/PMC6005683/ /pubmed/29846170 http://dx.doi.org/10.7554/eLife.34058 Text en © 2018, Spletter et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Spletter, Maria L
Barz, Christiane
Yeroslaviz, Assa
Zhang, Xu
Lemke, Sandra B
Bonnard, Adrien
Brunner, Erich
Cardone, Giovanni
Basler, Konrad
Habermann, Bianca H
Schnorrer, Frank
A transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle
title A transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle
title_full A transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle
title_fullStr A transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle
title_full_unstemmed A transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle
title_short A transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle
title_sort transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005683/
https://www.ncbi.nlm.nih.gov/pubmed/29846170
http://dx.doi.org/10.7554/eLife.34058
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