Abstract

Vertebrate segmentation is regulated by the “segmentation clock”, which drives cyclic expression of several genes in the caudal presomitic mesoderm (PSM). One such gene is Lunatic fringe (Lfng), which encodes a modifier of Notch signalling, and which is also expressed in a stripe at the cranial end of the PSM, adjacent to the newly forming somite border. We have investigated the functional requirements for these modes of Lfng expression during somitogenesis by generating mice in which Lfng is expressed in the cranial stripe but strongly reduced in the caudal PSM, and find that requirements for Lfng activity alter during axial growth. Formation of cervical, thoracic and lumbar somites/vertebrae, but not sacral and adjacent tail somites/vertebrae, depends on caudal, cyclic Lfng expression. Indeed, the sacral region segments normally in the complete absence of Lfng and shows a reduced requirement for another oscillating gene, Hes7, indicating that the architecture of the clock alters as segmentation progresses. We present evidence that Lfng controls dorsal-ventral axis specification in the tail, and also suggest that Lfng controls the expression or activity of a long-range signal that regulates axial extension.

Highlights

  • Somites are repeated epithelial blocks of tissue that differentiate into the segmental units of the axial skeleton, attached skeletal and limb muscles, and additional mesodermal tissues

  • We show that oscillatory Lunatic fringe (Lfng) expression in the caudal presomitic mesoderm (PSM) is required in the cranial body half, and that activity in the cranial Lfng stripe is required in the tail

  • The weakest BBL-2-rescued foetus shows three regular tail vertebrae. These results suggest that stripe expression of Lfng in the cranial PSM helps maintain somitogenesis in the tail

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Summary

Introduction

Somites are repeated epithelial blocks of tissue that differentiate into the segmental units of the axial skeleton (vertebrae, intervertebral discs, ribs), attached skeletal and limb muscles, and additional mesodermal tissues. Somites form between embryonic days E7.75 and E13.5 from the unsegmented, mesenchymal presomitic mesoderm (PSM), which lies towards the caudal end of the embryo. During this process, formation of new epithelial boundaries (every 2 h in the mouse) at the cranial end of the PSM generates a new, bilateral pair of somites. Expression of cycling genes is synchronised between neighbouring cells, but subject to phase delays along the length of the axis so that a wave of transcription appears to sweep cranially along the PSM, concomitant with the formation of a new pair of somites

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