A role for neural determination genes in specifying the dorsoventral identity of telencephalic neurons

  1. Carol Fode1,
  2. Qiufu Ma2,3,
  3. Simona Casarosa1,
  4. Siew-Lan Ang1,
  5. David J. Anderson2, and
  6. François Guillemot1,4
  1. 1Institut de Génétique et de Biologie Moléculaire et Cellulaire, Centre National de la Recherche Scientífique/Institut National de la Santé et de la Recherche Médicale (IGBMC, CNRS/INSERM); Université Louis Pasteur, BP163, Communauté Urbaine de Strasbourg, France; 2Howard Hughes Medical Institute, Division of Biology 216-76, California Institute of Technology, Pasadena, California 91125 USA

Abstract

Neurogenin1 (Ngn1), Neurogenin2(Ngn2), and Mash1 encode bHLH transcription factors with neuronal determination functions. In the telencephalon, theNgns and Mash1 are expressed at high levels in complementary dorsal and ventral domains, respectively. We found thatNgn function is required to maintain these two separate expression domains, as Mash1 expression is up-regulated in the dorsal telencephalon of Ngn mutant embryos. We have taken advantage of the replacement of the Ngns by Mash1 in dorsal progenitors to address the role of the neural determination genes in neuronal-type specification in the telencephalon. InNgn2 single and Ngn1; Ngn2 double mutants, a population of early born cortical neurons lose expression of dorsal-specific markers and ectopically express a subset of ventral telencephalic-specific markers. Analysis of Mash1; Ngn2double mutant embryos and of embryos carrying a Ngn2 toMash1 replacement mutation demonstrated that ectopic expression of Mash1 is required and sufficient to confer these ventral characteristics to cortical neurons. Our results indicate that in addition to acting as neuronal determinants, Mash1 andNgns play a role in the specification of dorsal-ventral neuronal identity, directly linking pathways of neurogenesis and regional patterning in the forebrain.

Keywords

Footnotes

  • Present address: 3Dana-Farber Cancer Institute, Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115 USA

  • 4 Corresponding author.

  • E-MAIL francois{at}igbmc.u-strasbg.fr; FAX (33)3-88-65-32-01.

    • Received August 9, 1999.
    • Accepted November 19, 1999.
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