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Single-cell transcriptomes and runx2b(−/−) mutants reveal the genetic signatures of intermuscular bone formation in zebrafish

Intermuscular bones (IBs) are mineralized spicules, present in the myosepta of many, but not all, teleost species. IBs are often small and sharp, and they consequently limit how the fish can be processed; the IBs may cause injury or trauma if lodged in consumers’ throats or mouths, and therefore aff...

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Autores principales: Nie, Chun-Hong, Wan, Shi-Ming, Chen, Yu-Long, Huysseune, Ann, Wu, Ya-Ming, Zhou, Jia-Jia, Hilsdorf, Alexandre Wagner Silva, Wang, Wei-Min, Witten, Paul Eckhard, Lin, Qiang, Gao, Ze-Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718792/
https://www.ncbi.nlm.nih.gov/pubmed/36478733
http://dx.doi.org/10.1093/nsr/nwac152
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author Nie, Chun-Hong
Wan, Shi-Ming
Chen, Yu-Long
Huysseune, Ann
Wu, Ya-Ming
Zhou, Jia-Jia
Hilsdorf, Alexandre Wagner Silva
Wang, Wei-Min
Witten, Paul Eckhard
Lin, Qiang
Gao, Ze-Xia
author_facet Nie, Chun-Hong
Wan, Shi-Ming
Chen, Yu-Long
Huysseune, Ann
Wu, Ya-Ming
Zhou, Jia-Jia
Hilsdorf, Alexandre Wagner Silva
Wang, Wei-Min
Witten, Paul Eckhard
Lin, Qiang
Gao, Ze-Xia
author_sort Nie, Chun-Hong
collection PubMed
description Intermuscular bones (IBs) are mineralized spicules, present in the myosepta of many, but not all, teleost species. IBs are often small and sharp, and they consequently limit how the fish can be processed; the IBs may cause injury or trauma if lodged in consumers’ throats or mouths, and therefore affect the appeal of the fish to many consumers. The development of IBs in teleosts is still not fully understood and the molecular basis of IB development remains to be established. Here, the characteristics of IB tissue are evaluated based on single-cell transcriptomics in wild-type zebrafish. The analysis defined 18 distinct cell types. Differentiation trajectories showed that IBs are derived from tendons and that a core tendon-osteoblast cell lineage is related to IB formation. In particular, the functions of 10 candidate genes were evaluated via CRISPR-Cas9 mutants. Among those, runx2b(−/−) mutants completely lost IBs, while swimming performance, growth and bone mineral density were not significantly different from runx2b(+/+) zebrafish. Comparative single-cell RNA sequencing (scRNA-seq) analysis in runx2b(−/−) and runx2b(+/+) zebrafish revealed the role of osteoblasts in IB formation. In addition, differentially expressed genes were enriched in the transforming growth factor β/bone morphogenetic protein (TGF-β/BMP) pathway after runx2b deletion. This study provides evidence for the crucial role of runx2b regulation in IB formation. Genetic breeding can target runx2b regulation and generate strains of commercial fish species without IBs, which can improve the safe consumption and economic value of many farmed fish species.
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spelling pubmed-97187922022-12-06 Single-cell transcriptomes and runx2b(−/−) mutants reveal the genetic signatures of intermuscular bone formation in zebrafish Nie, Chun-Hong Wan, Shi-Ming Chen, Yu-Long Huysseune, Ann Wu, Ya-Ming Zhou, Jia-Jia Hilsdorf, Alexandre Wagner Silva Wang, Wei-Min Witten, Paul Eckhard Lin, Qiang Gao, Ze-Xia Natl Sci Rev Research Article Intermuscular bones (IBs) are mineralized spicules, present in the myosepta of many, but not all, teleost species. IBs are often small and sharp, and they consequently limit how the fish can be processed; the IBs may cause injury or trauma if lodged in consumers’ throats or mouths, and therefore affect the appeal of the fish to many consumers. The development of IBs in teleosts is still not fully understood and the molecular basis of IB development remains to be established. Here, the characteristics of IB tissue are evaluated based on single-cell transcriptomics in wild-type zebrafish. The analysis defined 18 distinct cell types. Differentiation trajectories showed that IBs are derived from tendons and that a core tendon-osteoblast cell lineage is related to IB formation. In particular, the functions of 10 candidate genes were evaluated via CRISPR-Cas9 mutants. Among those, runx2b(−/−) mutants completely lost IBs, while swimming performance, growth and bone mineral density were not significantly different from runx2b(+/+) zebrafish. Comparative single-cell RNA sequencing (scRNA-seq) analysis in runx2b(−/−) and runx2b(+/+) zebrafish revealed the role of osteoblasts in IB formation. In addition, differentially expressed genes were enriched in the transforming growth factor β/bone morphogenetic protein (TGF-β/BMP) pathway after runx2b deletion. This study provides evidence for the crucial role of runx2b regulation in IB formation. Genetic breeding can target runx2b regulation and generate strains of commercial fish species without IBs, which can improve the safe consumption and economic value of many farmed fish species. Oxford University Press 2022-08-02 /pmc/articles/PMC9718792/ /pubmed/36478733 http://dx.doi.org/10.1093/nsr/nwac152 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nie, Chun-Hong
Wan, Shi-Ming
Chen, Yu-Long
Huysseune, Ann
Wu, Ya-Ming
Zhou, Jia-Jia
Hilsdorf, Alexandre Wagner Silva
Wang, Wei-Min
Witten, Paul Eckhard
Lin, Qiang
Gao, Ze-Xia
Single-cell transcriptomes and runx2b(−/−) mutants reveal the genetic signatures of intermuscular bone formation in zebrafish
title Single-cell transcriptomes and runx2b(−/−) mutants reveal the genetic signatures of intermuscular bone formation in zebrafish
title_full Single-cell transcriptomes and runx2b(−/−) mutants reveal the genetic signatures of intermuscular bone formation in zebrafish
title_fullStr Single-cell transcriptomes and runx2b(−/−) mutants reveal the genetic signatures of intermuscular bone formation in zebrafish
title_full_unstemmed Single-cell transcriptomes and runx2b(−/−) mutants reveal the genetic signatures of intermuscular bone formation in zebrafish
title_short Single-cell transcriptomes and runx2b(−/−) mutants reveal the genetic signatures of intermuscular bone formation in zebrafish
title_sort single-cell transcriptomes and runx2b(−/−) mutants reveal the genetic signatures of intermuscular bone formation in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718792/
https://www.ncbi.nlm.nih.gov/pubmed/36478733
http://dx.doi.org/10.1093/nsr/nwac152
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