Covassin Laurence, Amigo Julio D, Suzuki Kana, Teplyuk Viktor, Straubhaar Juerg, Lawson Nathan D
Program in Gene Function and Expression, University of Massachusetts Medical School, Lazare Research Building, Room 617, 364 Plantation Street, Worcester, MA 01605, USA.
Dev Biol. 2006 Nov 15;299(2):551-62. doi: 10.1016/j.ydbio.2006.08.020. Epub 2006 Aug 10.
In this study, we utilize fluorescent activated cell sorting (FACS) of cells from transgenic zebrafish coupled with microarray analysis to globally analyze expression of cell type specific genes. We find that it is possible to isolate cell populations from Tg(fli1:egfp)(y1) zebrafish embryos that are enriched in vascular, hematopoietic and pharyngeal arch cell types. Microarray analysis of GFP+ versus GFP- cells isolated from Tg(fli1:egfp)(y1) embryos identifies genes expressed in hematopoietic, vascular and pharyngeal arch tissue, consistent with the expression of the fli1:egfp transgene in these cell types. Comparison of expression profiles from GFP+ cells isolated from embryos at two different time points reveals that genes expressed in different fli1+ cell types display distinct temporal expression profiles. We also demonstrate the utility of this approach for gene discovery by identifying numerous previously uncharacterized genes that we find are expressed in fli1:egfp-positive cells, including new markers of blood, endothelial and pharyngeal arch cell types. In parallel, we have developed a database to allow easy access to both our microarray and in situ results. Our results demonstrate that this is a robust approach for identification of cell type specific genes as well as for global analysis of cell type specific gene expression in zebrafish embryos.
在本研究中,我们利用转基因斑马鱼细胞的荧光激活细胞分选(FACS)结合微阵列分析,对细胞类型特异性基因的表达进行全局分析。我们发现,从Tg(fli1:egfp)(y1)斑马鱼胚胎中分离出富含血管、造血和咽弓细胞类型的细胞群体是可行的。对从Tg(fli1:egfp)(y1)胚胎中分离出的GFP+与GFP-细胞进行微阵列分析,鉴定出在造血、血管和咽弓组织中表达的基因,这与fli1:egfp转基因在这些细胞类型中的表达一致。对从两个不同时间点的胚胎中分离出的GFP+细胞的表达谱进行比较,发现不同fli1+细胞类型中表达的基因具有不同的时间表达谱。我们还通过鉴定许多先前未表征的基因来证明这种方法在基因发现中的实用性,这些基因在fli1:egfp阳性细胞中表达,包括血液、内皮和咽弓细胞类型的新标记。同时,我们开发了一个数据库,以便轻松访问我们的微阵列和原位结果。我们的结果表明,这是一种用于鉴定细胞类型特异性基因以及对斑马鱼胚胎中细胞类型特异性基因表达进行全局分析的强大方法。