Cited by 63Developmental Biology and Gene RegulationGenomics and Chromatin DynamicsWnt/β-catenin signaling in development and cancer

The Snail repressor positions Notch signaling in the Drosophila embryo

Cowden, John, Levine, Michael·2002·Development

Abstract

The maternal Dorsal nuclear gradient initiates the differentiation of the mesoderm, neurogenic ectoderm and dorsal ectoderm in the precellular Drosophila embryo. Each tissue is subsequently subdivided into multiple cell types during gastrulation. We have investigated the formation of the mesectoderm within the ventral-most region of the neurogenic ectoderm. Previous studies suggest that the Dorsal gradient works in concert with Notch signaling to specify the mesectoderm through the activation of the regulatory gene sim within single lines of cells that straddle the presumptive mesoderm. This model was confirmed by misexpressing a constitutively activated form of the Notch receptor, Notch(IC), in transgenic embryos using the eve stripe2 enhancer. The Notch(IC) stripe induces ectopic expression of sim in the neurogenic ectoderm where there are low levels of the Dorsal gradient. sim is not activated in the ventral mesoderm, due to inhibition by the localized zinc-finger Snail repressor, which is selectively expressed in the ventral mesoderm. Additional studies suggest that the Snail repressor can also stimulate Notch signaling. A stripe2-snail transgene appears to induce Notch signaling in 'naïve' embryos that contain low uniform levels of Dorsal. We suggest that these dual activities of Snail, repression of Notch target genes and stimulation of Notch signaling, help define precise lines of sim expression within the neurogenic ectoderm.

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Crossref · 10.1242/dev.129.7.1785

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  • It is likely that Notch signaling is required for activation of sim and m8, which would explain their more refined expression domain.

    “It is likely that Notch signaling is required for activation of sim and m8, which would explain their more refined expression domain”

    From Graded dorsal and differential gene regulation in the Drosophila embryo. (2009) · cites this paper as Cowden and Levine 2002

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References 44 · Cited by 63

Authors
Cowden, J., & Levine, M.
Affiliations
University of California, Berkeley (US)
Venue
Development
Published
2002-04-01
Volume
129
Issue
7
Pages
1785-1793
ISSN
  • 0950-1991 (ISSN-L)
  • 1477-9129
OpenAlex
W2183610572
Cited by
63
References
44
Citations by year
2025: 1 · 2023: 2 · 2022: 2 · 2021: 3 · 2020: 2 · 2019: 4 · 2018: 2 · 2016: 4 · 2014: 2 · 2013: 2 · 2012: 1
FWCI
1.85
Type
journal article
Language
en
Open access
closed
Locations
  • Development (publishedVersion)
  • PubMed (publishedVersion)
  • HighWire Press Open Archive (submittedVersion)
Funders
National Institute of General Medical Sciences (GM-46638)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
Keywords
Notch signaling, ventral mesoderm, Drosophila embryo, transcriptional repression, gastrulation, cell fate specification
MeSH terms
Snail Family Transcription Factors, Animals, DNA-Binding Proteins, Drosophila, Female, Genes, Regulator, Membrane Proteins, Mutation, Nuclear Proteins, Phosphoproteins, Repressor Proteins, Transcription Factors, Signal Transduction, Genes, Insect, In Situ Hybridization, Gene Expression Regulation, Developmental, Drosophila Proteins, Animals, Genetically Modified, Basic Helix-Loop-Helix Proteins, Receptors, Notch

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