|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 121, Issue 2 429-438, Copyright © 1995 by Company of Biologists
JOURNAL ARTICLES |
A Giangrande
Institut de Genetique et de Biologie Molecularie et Cellulaire, CNRS UPR6520-INSERM U. 184-ULP, Illkirch, CU de Strasbourg, France.
Fly glial cells in the wing peripheral nervous system of Drosophila melanogaster originate from underlying epithelial cells. Two findings indicate that gliogenesis is closely associated with neurogenesis. First, it only occurs in regions that also give rise to sensory organs. Second, in mutants that induce the development of ectopic sensory organs glial cells develop at new positions. These findings prompted a genetic analysis to establish whether glial and sensory organ differentiation depend on the same genes. Loss of function mutations of the achaete-scute complex lead to a significant reduction of sensory bristles and glial cells. Genes within the complex affect gliogenesis with different strength and display some functional redundancy. Thus, neurogenesis and gliogenesis share the same genetic pathway. Despite these similarities, however, the mechanism of action of the achaete-scute complex seems to be different in the two processes. Neural precursors express products of the complex, therefore the role of these genes on neurogenesis is direct. However, markers specific to glial cells do not colocalize with products of the achaete-scute complex, showing that the complex affects gliogenesis indirectly. These observations lead to the hypothesis that gliogenesis is induced by the presence of sensory organ cells, either the precursor or its progeny.
This article has been cited by other articles:
![]() |
M. Schubiger, C. Carre, C. Antoniewski, and J. W. Truman Ligand-dependent de-repression via EcR/USP acts as a gate to coordinate the differentiation of sensory neurons in the Drosophila wing Development, December 1, 2005; 132(23): 5239 - 5248. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Aigouy, V. Van de Bor, M. Boeglin, and A. Giangrande Time-lapse and cell ablation reveal the role of cell interactions in fly glia migration and proliferation Development, October 15, 2004; 131(20): 5127 - 5138. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Van De Bor, P. Heitzler, S. Leger, C. Plessy, and A. Giangrande Precocious Expression of the Glide/Gcm Glial-Promoting Factor in Drosophila Induces Neurogenesis Genetics, March 1, 2002; 160(3): 1095 - 1106. [Abstract] [Full Text] [PDF] |
||||
![]() |
V Van De Bor and A Giangrande Notch signaling represses the glial fate in fly PNS Development, January 4, 2001; 128(8): 1381 - 1390. [Abstract] [PDF] |
||||
![]() |
V Van De Bor, R Walther, and A Giangrande Some fly sensory organs are gliogenic and require glide/gcm in a precursor that divides symmetrically and produces glial cells Development, January 9, 2000; 127(17): 3735 - 3743. [Abstract] [PDF] |
||||
![]() |
G. Reddy and V Rodrigues A glial cell arises from an additional division within the mechanosensory lineage during development of the microchaete on the Drosophila notum Development, January 10, 1999; 126(20): 4617 - 4622. [Abstract] [PDF] |
||||
![]() |
M Gho, Y Bellaiche, and F Schweisguth Revisiting the Drosophila microchaete lineage: a novel intrinsically asymmetric cell division generates a glial cell Development, January 8, 1999; 126(16): 3573 - 3584. [Abstract] [PDF] |
||||
![]() |
R Bernardoni, A. Miller, and A Giangrande Glial differentiation does not require a neural ground state Development, January 8, 1998; 125(16): 3189 - 3200. [Abstract] [PDF] |
||||
![]() |
S Vincent, J. Vonesch, and A Giangrande Glide directs glial fate commitment and cell fate switch between neurones and glia Development, January 1, 1996; 122(1): 131 - 139. [Abstract] [PDF] |
||||