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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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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. |
format | Online Article Text |
id | pubmed-6005683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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