Cited by 162Developmental Biology and Gene RegulationNeurogenesis and neuroplasticity mechanismsNeurobiology and Insect Physiology Research

Dorsoventral patterning in the Drosophila central nervous system: the vnd homeobox gene specifies ventral column identity

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McDonald, Jocelyn A., Holbrook, Scott, Isshiki, Takako, Weiss, Joseph, Doe, Chris Q., Mellerick, Dervla M.·1998·Genes & Development

Abstract

The Drosophila CNS develops from three columns of neuroectodermal cells along the dorsoventral (DV) axis: ventral, intermediate, and dorsal. In this and the accompanying paper, we investigate the role of two homeobox genes, vnd and ind , in establishing ventral and intermediate cell fates within the Drosophila CNS. During early neurogenesis, Vnd protein is restricted to ventral column neuroectoderm and neuroblasts; later it is detected in a complex pattern of neurons. We use molecular markers that distinguish ventral, intermediate, and dorsal column neuroectoderm and neuroblasts, and a cell lineage marker for selected neuroblasts, to show that loss of vnd transforms ventral into intermediate column identity and that specific ventral neuroblasts fail to form. Conversely, ectopic vnd produces an intermediate to ventral column transformation. Thus, vnd is necessary and sufficient to induce ventral fates and repress intermediate fates within the Drosophila CNS. Vertebrate homologs of vnd ( Nkx2.1 and 2.2 ) are similarly expressed in the ventral CNS, raising the possibility that DV patterning within the CNS is evolutionarily conserved.

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  1. Campos-Ortega, J.A. 1993. Early neurogenesis in Drosophila melanogaster. In Development of Drosophila melanogaster (ed. M. Bate and A. Martinez-Arias), pp. 1091-1130. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
  2. Spradling, A.C. 1986. P-element-mediated transformation. In Drosophila: A practical approach (ed. D.B. Roberts), pp. 175- 197. IRL Press, Oxford, UK.
  3. Srinivasan, S., C.-Y. Peng, S. Nair, J.B. Skeath, E.P. Spana, and C.Q. Doe. 1998. Biochemical analysis of Prospero protein during aymmetric cell division: Cortical Prospero is highly phosphorylated relative to nuclear Prospero. Dev. Biol. (in press).

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Authors
McDonald, J. A., Holbrook, S., Isshiki, T., Weiss, J., Doe, C. Q., & Mellerick, D. M.
Affiliations
Howard Hughes Medical Institute (US)
Venue
Genes & Development
Published
1998-11-15
Volume
12
Issue
22
Pages
3603-3612
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2109597876
Cited by
162
References
4
Citations by year
2026: 6 · 2025: 5 · 2024: 1 · 2023: 2 · 2022: 6 · 2021: 3 · 2020: 4 · 2019: 5 · 2018: 2 · 2017: 4 · 2016: 4 · 2015: 7 · 2014: 1 · 2013: 9 · 2012: 1
Type
posted content
Language
en
Open access
Locations
  • Genes & Development (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Science Foundation
  • National Institutes of Health
  • University of Illinois at Urbana-Champaign
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
Keywords
dorsoventral patterning, Drosophila central nervous system, neuroectoderm, neuroblasts, cell fate specification, TTF-1, Nkx2.2
MeSH terms
Animals, Central Nervous System, Drosophila, Genes, Homeobox, Immunohistochemistry, Neurons, Transcription Factors, Homeodomain Proteins, Gene Expression Regulation, Developmental, Body Patterning, Drosophila Proteins

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