Expression profiling of glial genes during Drosophila embryogenesis

被引:57
作者
Altenhein, Benjamin
Becker, Angela
Busold, Christian
Beckmann, Boris
Hoheisel, Joerg D.
Technau, Gerhard M. [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Genet Inst, D-6500 Mainz, Germany
[2] Deutsch Krebsforschungszentrum, Div Funct Genome Anal, D-6900 Heidelberg, Germany
关键词
glial development; gcm; glial genes; microarrays; Drosophila embryogenesis;
D O I
10.1016/j.ydbio.2006.04.460
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the central nervous system of Drosophila, the induction of the glial cell fate is dependent on the transcription factor glial cells missing (gcm). Though a considerable number of other genes have been shown to be expressed in all or in subsets of glial cells, the course of glial cell differentiation and subtype specification is only poorly understood. This prompted us to design a whole genome microarray approach comparing gem gain-of-function and, for the first time, gem loss-of-function genetics to wildtype in time course experiments along embryogenesis. The microarray data were analyzed with special emphasis on the temporal profile of differential regulation. A comparison of both experiments enabled us to identify more than 300 potential gcm target genes. Validation by in situ hybridization revealed expression in glial cells, macrophages, and tendon cells (all three cell types depend on gem) for 70 genes, of which more than 50 had been unknown to be under gem control. Eighteen genes are exclusively expressed in glial cells, and their dependence on gem was confirmed in situ. Initial considerations regarding the role of the newly discovered glial genes are discussed based on gene ontology and the temporal profile and subtype specificity of their expression. This collection of glial genes provides an important basis for the clarification of the genetic network controlling various aspects of glial development and function. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:545 / 560
页数:16
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