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首页> 外文期刊>Developmental biology >Identification of a retina-specific Otx2 enhancer element active in immature developing photoreceptors.
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Identification of a retina-specific Otx2 enhancer element active in immature developing photoreceptors.

机译:鉴定在发育中的未成熟感光体中活跃的视网膜特异性Otx2增强子元件。

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The homeodomain protein, Otx2, is a critical regulator of vertebrate photoreceptor genesis. However, the genetic elements that define the expression of Otx2 during photoreceptor development are unknown. Therefore, we sought to identify an Otx2 enhancer element that functions in photoreceptor development in order to better understand this specification event. Using the technique of electroporation, we tested a number of evolutionarily conserved elements (ECRs) for expression in the developing retina, and identified ECR2 as having robust activity in the retina. We have characterized this element using a number of assays, including Cre-fate mapping experiments. We found that ECR2 recapitulates expression/function of Otx2 primarily in newly postmitotic photoreceptor cells (PRs), as well as in a subset of retinal progenitor cells (RPCs). ECR2 was also found to be expressed in a subset of horizontal cells (HCs), in keeping with the role of Otx2 in HC development. Furthermore, we determined that the ECR2 element is not active in other Otx2-positive cells such as retinal bipolar cells (BPs), retinal pigmented epithelium (RPE), or the tectum, suggesting that the transcriptional networks controlling Otx2 expression in these cells are unique from those of developing PRs and HCs. These results reveal a distinct molecular state in dividing retinal cells and their newly postmitotic progeny, and provide genetic access to an early and critical transcriptional node involved in the genesis of vertebrate PRs.
机译:同源结构域蛋白Otx2是脊椎动物感光细胞发生的关键调控因子。但是,在光感受器发育过程中定义Otx2表达的遗传元件尚不清楚。因此,我们试图确定一个Otx2增强子元件,该元件在感光器的开发中发挥作用,以便更好地理解此规范事件。使用电穿孔技术,我们测试了在发育中的视网膜中表达的许多进化保守元件(ECR),并确定了ECR2在视网膜中具有强大的活性。我们已经使用许多测定法(包括Cre-fate映射实验)对该元素进行了表征。我们发现ECR2主要在新的有丝分裂后感光细胞(PRs)以及视网膜祖细胞(RPCs)的子集中概括了Otx2的表达/功能。还发现ECR2在水平细胞(HC)的子集中表达,与Otx2在HC发育中的作用保持一致。此外,我们确定ECR2元件在其他Otx2阳性细胞(例如视网膜双极细胞(BPs),视网膜色素上皮细胞(RPE)或子宫顶盖)中不活跃,表明控制这些细胞中Otx2表达的转录网络是独特的来自发展中的PR和HC。这些结果揭示了在分裂视网膜细胞及其新的有丝分裂后代后代中的独特分子状态,并为涉及脊椎动物PRs发生的早期和关键转录节点提供了遗传途径。

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