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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Main Authors: Yin, Jianmin, Lee, Raymond, Ono, Yosuke, Ingham, Philip William, Saunders, Timothy E.
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/144211
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Institution: Nanyang Technological University
Language: English
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spelling 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.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Biological sciences
Adaxial Cells
Fast Muscle Fibers
spellingShingle 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
description 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)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Yin, Jianmin
Lee, Raymond
Ono, Yosuke
Ingham, Philip William
Saunders, Timothy E.
format Article
author Yin, Jianmin
Lee, Raymond
Ono, Yosuke
Ingham, Philip William
Saunders, Timothy E.
author_sort 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
publishDate 2020
url https://hdl.handle.net/10356/144211
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