Projects per year
Abstract / Description of output
The mesodermal germ layer is patterned into mediolateral subtypes by signaling factors including BMP and FGF. How these pathways are integrated to induce specific mediolateral cell fates is not well understood. We used mesoderm derived from post-gastrulation neuromesodermal progenitors (NMPs), which undergo a binary mediolateral patterning decision, as a simplified model to understand how FGF acts together with BMP to impart mediolateral fate. Using zebrafish and mouse NMPs, we identify an evolutionarily conserved mechanism of BMP and FGF mediated mediolateral mesodermal patterning that occurs through modulation of basic helix-loop-helix (bHLH) transcription factor activity. BMP imparts lateral fate through induction of Id helix loop helix (HLH) proteins, which antagonize bHLH transcription factors, induced by FGF signaling, that specify medial fate. We extend our analysis of zebrafish development to show that bHLH activity is responsible for the mediolateral patterning of the entire mesodermal germ layer.
Original language | English |
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Number of pages | 27 |
Journal | eLIFE |
Volume | 7 |
Early online date | 7 Jun 2018 |
DOIs | |
Publication status | E-pub ahead of print - 7 Jun 2018 |
Keywords / Materials (for Non-textual outputs)
- BMP
- FGF
- bHLH
- developmental biology
- mesoderm
- morphogen
- mouse
- neuromesodermal progenitor
- regenerative medicine
- stem cells
- zebrafish
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Dive into the research topics of 'BMP and FGF signaling interact to pattern mesoderm by controlling basic helix-loop-helix transcription factor activity'. Together they form a unique fingerprint.Projects
- 2 Finished
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Specification, maintenance and elimination of stem cell progenitors for the mammalian anteroposterior axis
1/01/13 → 31/12/18
Project: Research
Profiles
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Sally Lowell
- School of Biological Sciences - Personal Chair of Stem Cell Biology and Early Development
- Centre for Regenerative Medicine
- Edinburgh Neuroscience
Person: Academic: Research Active