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Prediction of cis-regulatory elements controlling genes differentially expressed by retinal and choroidal vascular endothelial cells

机译:视网膜和脉络膜血管内皮细胞差异表达基因的顺式调控元件的预测

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摘要

Cultured endothelial cells of the human retina and choroid demonstrate distinct patterns of gene expression. We hypothesized that differential gene expression reflected differences in the interactions of transcription factors and respective cis-regulatory motifs(s) in these two endothelial cell subpopulations, recognizing that motifs often exist as modules. We tested this hypothesis in silico by using TRANSFAC Professional and CisModule to identify cis-regulatory motifs and modules in genes that were differentially expressed by human retinal versus choroidal endothelial cells, as identified by analysis of a microarray data set. Motifs corresponding to eight transcription factors were significantly (p < 0.05) differentially abundant in genes that were relatively highly expressed in retinal (i.e., glucocorticoid receptor, high mobility group AT-hook 1, heat shock transcription factor 1, p53, vitamin D receptor) or choroidal (i.e., transcription factor E2F, Yin Yang 1, zinc finger 5) endothelial cells. Predicted cis-regulatory modules were quite different for these two groups of genes. Our findings raise the possibility of exploiting specific cis-regulatory motifs to target therapy at the ocular endothelial cells subtypes responsible for neovascular age-related macular degeneration or proliferative diabetic retinopathy.Electronic supplementary materialThe online version of this article (doi:10.1007/s12177-008-9007-1) contains supplementary material, which is available to authorized users.
机译:人视网膜和脉络膜的培养的内皮细胞显示出不同的基因表达模式。我们假设差异基因表达反映了这两个内皮细胞亚群中转录因子和各自的顺式调控基序相互作用的差异,认识到基序通常作为模块存在。我们通过使用TRANSFAC Professional和CisModule在计算机上测试了这一假设,以鉴定由人视网膜与脉络膜内皮细胞差异表达的基因中的顺式调控基序和模块,如通过微阵列数据集的分析所确定的。对应于八个转录因子的基序在视网膜中相对高表达的基因(即糖皮质激素受体,高迁移率AT钩1,热休克转录因子1,p53,维生素D受体)中显着(p <0.05)差异丰富。或脉络膜(即转录因子E2F,阴阳1,锌指5)内皮细胞。对于这两组基因,预测的顺式调控模块非常不同。我们的发现提高了利用特定的顺式调控基序靶向治疗与新生血管性年龄相关性黄斑变性或增生性糖尿病性视网膜病相关的眼内皮细胞亚型的可能性。电子补充材料本文的在线版本(doi:10.1007 / s12177-008 -9007-1)包含补充材料,授权用户可以使用。

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