Figure 6
Figure 6. Overexpression of the Lycat transgene specifically increased hematopoietic and endothelial gene expression in EBs using a microarray analysis. We identified differentially expressed genes between VC and FC5 ES cell-derived D4 EBs using SmartArray (CapitalBio, Beijing, China) chips containing about 25 000 mouse genes. The top 200 affected genes were shown to be up- and down-regulated from 2- to 37-fold (averaged from 2 independent experiments) in FC5 EBs, of which 65 genes are related to hemangioblastic, hematopoietic, and endothelial lineages. Thirty-five of these genes and HoxB1 (1.5-fold decrease) were chosen and verified by Q-PCR. These genes were clustered into mesoderm/hemangioblast genes (A), endothelial genes (B), hematopoietic genes (C), cardiac genes (D), Hox family genes (E), and pluripotency genes (F). Q-PCR was carried out using SYBR Green, and RNA levels were normalized by GAPDH. Error bars represent standard deviations

Overexpression of the Lycat transgene specifically increased hematopoietic and endothelial gene expression in EBs using a microarray analysis. We identified differentially expressed genes between VC and FC5 ES cell-derived D4 EBs using SmartArray (CapitalBio, Beijing, China) chips containing about 25 000 mouse genes. The top 200 affected genes were shown to be up- and down-regulated from 2- to 37-fold (averaged from 2 independent experiments) in FC5 EBs, of which 65 genes are related to hemangioblastic, hematopoietic, and endothelial lineages. Thirty-five of these genes and HoxB1 (1.5-fold decrease) were chosen and verified by Q-PCR. These genes were clustered into mesoderm/hemangioblast genes (A), endothelial genes (B), hematopoietic genes (C), cardiac genes (D), Hox family genes (E), and pluripotency genes (F). Q-PCR was carried out using SYBR Green, and RNA levels were normalized by GAPDH. Error bars represent standard deviations

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