Microarray analysis of Tbx2-directed gene expression:: a possible role in osteogenesis

被引:44
作者
Chen, JR
Zhong, Q
Wang, J
Cameron, RS
Borke, JL
Isales, CM
Bollag, RJ [1 ]
机构
[1] Program Dev Biol, Augusta, GA 30912 USA
[2] Med Coll Georgia, Inst Mol Med & Genet, Programs Cell Signaling, Augusta, GA 30912 USA
[3] Med Coll Georgia, Dept Cell Biol & Anat, Augusta, GA 30912 USA
[4] Med Coll Georgia, Dept Oral Biol, Augusta, GA 30912 USA
[5] Med Coll Georgia, Dept Med, Augusta, GA 30912 USA
[6] Med Coll Georgia, Augusta VA Med Ctr, Augusta, GA 30904 USA
[7] Cellom Inc, Pittsburgh, PA 15238 USA
关键词
microarray; T-box genes; gene expression; bone; cartilage; cell cycle; cell adhesion;
D O I
10.1016/S0303-7207(01)00456-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tbx2 is a member of the developmentally important transcriptional regulatory T-box gene family, whose target genes have not been well characterized. In an attempt to identify genes that may be regulated by Tbx2, mouse cDNA microarrays were used to analyze differential gene expression profiles, comparing stably transfected NIH3T3 cells overexpressing Tbx2 and vector-transfected controls. Among 8734 genes, 107 genes were up-regulated by 2-fold or greater, and 66 genes were down-regulated by 2-fold or greater. Caveolin, pleiotrophin (osf-1), osteoblast-specific factor-2 (osf-2) and collagen type Iv. were among the genes upregulated in the Tbx2-overexpressing, cells, whereas cadherin 3. tenascin C, and insulin-like growth factor binding protein 10/CYR61 (IBP10) were among the genes downregulated. Northern blot analysis confirmed the correlation of expression of several genes, including IBP10 and osf-2, in fibroblast NIH3T3 and rat osteosarcoma ROS17/2.8 cells differentially expressing Tbx2. In ROS17/2.8 cells transfected with antisense Tbx2, osf-2 was downregulated, whereas transfection of sense Tbx2 upregulated this gene. Interestingly, the expression of pleiotrophin (osf-1) and collagen I alpha with Tbx2 transfection showed an inverse regulatory correlation between NIH3T3 and ROS17/2.8 cells. Thus, Tbx2 can act as both a repressor and activator, and the cellular context can influence the effect on gene expression. Although the data do not address whether Tbx2 directly mediates the transcriptional effect, a number of candidate genes possess putative T-box gene regulatory elements. The results support the hypothesis that Tbx2 may be an important modulator of bone development. Further functional cluster analysis indicates that Tbx2 might also be involved in the regulation of cell cycle and cell adhesion. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:43 / 54
页数:12
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