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CNS midline cells contribute to maintenance of the initial dorsoventral patterning of theDrosophila ventral neuroectoderm

Authors :
In Ok Kim
Sang Hee Kim
Pyung Lim Han
Sang-Hak Jeon
In Chul Kim
Yeon Kyung Kwon
Sunmi Kim
Source :
Journal of Neurobiology. 62:397-405
Publication Year :
2005
Publisher :
Wiley, 2005.

Abstract

Dorsoventral patterning of the Drosophila ventral neuroectoderm is established by the expression of three evolutionarily conserved homeodomain genes: ventral nervous system defective (vnd), intermediate neuroblasts defective (ind), and muscle segment homeobox (msh) in the medial, intermediate, and lateral columns of the ventral neuroectoderm, respectively. It was not clear whether extrinsic factor(s) from the CNS midline cells influence the initial dorsoventral patterning by controlling the expression of the dorsoventral patterning genes. We show here that the CNS midline cells, specified by single-minded (sim), are essential for maintaining expression of the dorsoventral patterning genes. Ectopic expression of sim in the ventral neuroectoderm during the blastoderm stage repressed expression of the three homeodomain genes in the ventral neuroectoderm. This indicates that the identity of the CNS midline cells is established by a series of repressions of the three homeodomain genes in the ventral neuroectoderm. Ectopic expression of sim in the ventral neuroectoderm during initial neurogenesis induced ectopic ind expression in the medial column in addition to that in the intermediate column via EGFR signaling between the ventral neuroectoderm and midline cells. In contrast, it repressed the expression of vnd and msh in the medial and lateral columns, respectively. Our findings demonstrate that the CNS midline cells provide extrinsic positional information via EGFR signaling that maintains the initial subdivision of the ventral neuroectoderm into three dorsoventral columns during initial neurogenesis.

Details

ISSN :
10974695 and 00223034
Volume :
62
Database :
OpenAIRE
Journal :
Journal of Neurobiology
Accession number :
edsair.doi.dedup.....899522c4316087a19256d0d4ee86ece4