Spatiotemporal coordination of FGF and Shh signaling underlies the specification of myoblasts in the zebrafish embryo
Somitic cells give rise to a variety of cell types in response to Hh, BMP, and FGF signaling. Cell position within the developing zebrafish somite is highly dynamic: how, when, and where these signals specify cell fate is largely unknown. Combining four-dimensional imaging with pathway perturbations...
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sg-ntu-dr.10356-1442112023-09-27T13:04:00Z Spatiotemporal coordination of FGF and Shh signaling underlies the specification of myoblasts in the zebrafish embryo Yin, Jianmin Lee, Raymond Ono, Yosuke Ingham, Philip William Saunders, Timothy E. Lee Kong Chian School of Medicine (LKCMedicine) Science::Biological sciences Adaxial Cells Fast Muscle Fibers Somitic cells give rise to a variety of cell types in response to Hh, BMP, and FGF signaling. Cell position within the developing zebrafish somite is highly dynamic: how, when, and where these signals specify cell fate is largely unknown. Combining four-dimensional imaging with pathway perturbations, we characterize the spatiotemporal specification and localization of somitic cells. Muscle formation is guided by highly orchestrated waves of cell specification. We find that FGF directly and indirectly controls the differentiation of fast and slow-twitch muscle lineages, respectively. FGF signaling imposes tight temporal control on Shh induction of slow muscles by regulating the time at which fast-twitch progenitors displace slow-twitch progenitors from contacting the Shh-secreting notochord. Further, we find a reciprocal regulation of fast and slow muscle differentiation, morphogenesis, and migration. In conclusion, robust cell fate determination in the developing somite requires precise spatiotemporal coordination between distinct cell lineages and signaling pathways. Agri-Food and Veterinary Authority of Singapore (AVA) National Research Foundation (NRF) We wish to thank the IMCB fish facility for support. We thank Tom Carney (Nanyang Technological University, Singapore) for helpful suggestions and for sharing reagents. J.Y. and T.E.S. were supported by a National Research Foundation Singapore Fellowship awarded to T.E.S. ( NRF2012NRF-NRFF001-094 ). P.W.I. held a Toh Kian Chui Foundation endowed chair, which supported Y.O. R.L. was supported by IMCB core funding awarded to P.W.I. 2020-10-21T02:26:55Z 2020-10-21T02:26:55Z 2018 Journal Article Yin, J., Lee, R., Ono, Y., Ingham, P. W., & Saunders, T. E. (2018). Spatiotemporal coordination of FGF and Shh signaling underlies the specification of myoblasts in the zebrafish embryo. Developmental Cell, 46(6), 735-750. doi:10.1016/j.devcel.2018.08.024 1878-1551 https://hdl.handle.net/10356/144211 10.1016/j.devcel.2018.08.024 30253169 6 46 735 750 en Developmental Cell © 2018 Elsevier Inc. All rights reserved. |
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Science::Biological sciences Adaxial Cells Fast Muscle Fibers |
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Science::Biological sciences Adaxial Cells Fast Muscle Fibers Yin, Jianmin Lee, Raymond Ono, Yosuke Ingham, Philip William Saunders, Timothy E. Spatiotemporal coordination of FGF and Shh signaling underlies the specification of myoblasts in the zebrafish embryo |
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Somitic cells give rise to a variety of cell types in response to Hh, BMP, and FGF signaling. Cell position within the developing zebrafish somite is highly dynamic: how, when, and where these signals specify cell fate is largely unknown. Combining four-dimensional imaging with pathway perturbations, we characterize the spatiotemporal specification and localization of somitic cells. Muscle formation is guided by highly orchestrated waves of cell specification. We find that FGF directly and indirectly controls the differentiation of fast and slow-twitch muscle lineages, respectively. FGF signaling imposes tight temporal control on Shh induction of slow muscles by regulating the time at which fast-twitch progenitors displace slow-twitch progenitors from contacting the Shh-secreting notochord. Further, we find a reciprocal regulation of fast and slow muscle differentiation, morphogenesis, and migration. In conclusion, robust cell fate determination in the developing somite requires precise spatiotemporal coordination between distinct cell lineages and signaling pathways. |
author2 |
Lee Kong Chian School of Medicine (LKCMedicine) |
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Lee Kong Chian School of Medicine (LKCMedicine) Yin, Jianmin Lee, Raymond Ono, Yosuke Ingham, Philip William Saunders, Timothy E. |
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Article |
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Yin, Jianmin Lee, Raymond Ono, Yosuke Ingham, Philip William Saunders, Timothy E. |
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Yin, Jianmin |
title |
Spatiotemporal coordination of FGF and Shh signaling underlies the specification of myoblasts in the zebrafish embryo |
title_short |
Spatiotemporal coordination of FGF and Shh signaling underlies the specification of myoblasts in the zebrafish embryo |
title_full |
Spatiotemporal coordination of FGF and Shh signaling underlies the specification of myoblasts in the zebrafish embryo |
title_fullStr |
Spatiotemporal coordination of FGF and Shh signaling underlies the specification of myoblasts in the zebrafish embryo |
title_full_unstemmed |
Spatiotemporal coordination of FGF and Shh signaling underlies the specification of myoblasts in the zebrafish embryo |
title_sort |
spatiotemporal coordination of fgf and shh signaling underlies the specification of myoblasts in the zebrafish embryo |
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2020 |
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https://hdl.handle.net/10356/144211 |
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1779156749226344448 |