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Cited by 235

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Notch signaling regulates left–right asymmetry determination by inducing Nodal expression

Open access
Krebs, Luke T., Iwai, Naomi, Nonaka, Shigenori, Welsh, Ian C., Lan, Yu, Jiang, Rulang, Saijoh, Yukio, O'Brien, Timothy P., Hamada, Hiroshi, Gridley, Thomas·2003·Genes & Development

Abstract

Generation of left–right asymmetry is an integral part of the establishment of the vertebrate body plan. Here we show that the Notch signaling pathway plays a primary role in the establishment of left–right asymmetry in mice by directly regulating expression of the Nodal gene. Embryos mutant for the Notch ligand Dll1 or doubly mutant for the Notch1 and Notch2 receptors exhibit multiple defects in left–right asymmetry. Analysis of the enhancer regulating node-specific Nodal expression revealed the presence of binding sites for the RBP-J protein, the primary transcriptional mediator of Notch signaling. Mutation of these sites destroyed the ability of this enhancer to direct node-specific gene expression in transgenic mice. Our results demonstrate that Dll1-mediated Notch signaling is essential for generation of left–right asymmetry, and that the Notch pathway acts upstream of Nodal expression during left–right asymmetry determination in mice.

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Metadata

Authors
Krebs, L. T., Iwai, N., Nonaka, S., Welsh, I. C., Lan, Y., Jiang, R., Saijoh, Y., O'Brien, T. P., Hamada, H., & Gridley, T.
Venue
Genes & Development
Published
2003-05-02
Volume
17
Issue
10
Pages
1207-1212
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W1976943279
Cited by
235
References
0
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: Notch signaling regulates left–right asymmetry determination by inducing Nodal expression. https://app.cochat.ai/papers/10.1101/gad.1084703
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Krebs, L. T., Iwai, N., Nonaka, S., Welsh, I. C., Lan, Y., Jiang, R., Saijoh, Y., O'Brien, T. P., Hamada, H., & Gridley, T. (2003). Notch signaling regulates left–right asymmetry determination by inducing Nodal expression. Genes & Development. https://doi.org/10.1101/gad.1084703

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