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• W3102776214 abstract "During vertebrate development, the presomitic mesoderm (PSM) periodically segments into somites, which will form the segmented vertebral column and associated muscle, connective tissue, and dermis. The periodicity of somitogenesis is regulated by a segmentation clock of oscillating Notch activity. Here, we examined mouse mutants lacking only Fgf4 or Fgf8 , which we previously demonstrated act redundantly to prevent PSM differentiation. Fgf8 is not required for somitogenesis, but Fgf4 mutants display a range of vertebral defects. We analyzed Fgf4 mutants by quantifying mRNAs fluorescently labeled by hybridization chain reaction within Imaris-based volumetric tissue subsets. These data indicate that FGF4 maintains Hes7 levels and normal oscillatory patterns. To support our hypothesis that FGF4 regulates somitogenesis through Hes7 , we demonstrate genetic synergy between Hes7 and Fgf4 , but not with Fgf8 . Our data indicate that Fgf4 is potentially important in a spectrum of human Segmentation Defects of the Vertebrae caused by defective Notch oscillations." @default.
• W3102776214 created "2020-11-23" @default.
• W3102776214 creator A5018917055 @default.
• W3102776214 creator A5058427531 @default.
• W3102776214 creator A5064610754 @default.
• W3102776214 creator A5066596486 @default.
• W3102776214 date "2020-11-19" @default.
• W3102776214 modified "2023-10-17" @default.
• W3102776214 title "Fgf4 maintains Hes7 levels critical for normal somite segmentation clock function" @default.
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• W3102776214 doi "https://doi.org/10.7554/elife.55608" @default.
• W3102776214 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7717904" @default.
• W3102776214 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33210601" @default.
• W3102776214 hasPublicationYear "2020" @default.
• W3102776214 type Work @default.
• W3102776214 sameAs 3102776214 @default.
• W3102776214 citedByCount "27" @default.

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