Factorial microarray analysis of zebrafish retinal development

被引:37
|
作者
Leung, Yuk Fai [1 ,2 ]
Ma, Ping [3 ,4 ]
Link, Brian A. [5 ]
Dowling, John E. [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
[3] Univ Illinois, Dept Stat, Champaign, IL 61820 USA
[4] Univ Illinois, Inst Genom Biol, Champaign, IL 61820 USA
[5] Med Coll Wisconsin, Dept Cell Biol Neurobiol & Anat, Milwaukee, WI 53226 USA
基金
美国国家科学基金会;
关键词
Brg1-regulated genes; neuronal differentiation; cellular differentiation; signal transduction pathways; transcription factors;
D O I
10.1073/pnas.0806038105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In a zebrafish recessive mutant young (yng), retinal cells are specified to distinct cell classes, but they fail to morphologically differentiate. A null mutation in a brahma-related gene 1 (brg1) is responsible for this phenotype. To identify retina-specific Brg1-regulated genes that control cellular differentiation, we conducted a factorial microarray analysis. Gene expression profiles were compared from wild-type and yng retinas and stage-matched whole embryos at 36 and 52 hours postfertilization (hpf). From our analysis, three categories of genes were identified: (i) Brg1-regulated retinal differentiation genes (731 probesets), (ii) retina-specific genes independent of Brg1 regulation (3,038 probesets), and (iii) Brg1-regulated genes outside the retina (107 probesets). Biological significance was confirmed by further analysis of components of the Cdk5 signaling pathway and lrx transcription factor family, representing genes identified in category 1. This study highlights the utility of factorial microarray analysis to efficiently identify relevant regulatory pathways influenced by both specific gene products and normal developmental events.
引用
收藏
页码:12909 / 12914
页数:6
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