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Distinct cis-acting regions control six6 expression during eye field and optic cup stages of eye formation

机译:不同的顺式作用区域控制眼球形成阶段和视杯阶段的六六表达

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摘要

The eye field transcription factor, Six6, is essential for both the early (specification and proliferative growth) phase of eye formation, as well as for normal retinal progenitor cell differentiation. While genomic regions driving six6 optic cup expression have been described, the sequences controlling eye field and optic vesicle expression are unknown. Two evolutionary conserved regions 5′ and a third 3′ to the six6 coding region were identified, and together they faithfully replicate the endogenous X. laevis six6 expression pattern. Transgenic lines were generated and used to determine the onset and expression patterns controlled by the regulatory regions. The conserved 3′ region was necessary and sufficient for eye field and optic vesicle expression. In contrast, the two conserved enhancer regions located 5′ of the coding sequence were required together for normal optic cup and mature retinal expression. Gain-of-function experiments indicate endogenous six6 and GFP expression in F1 transgenic embryos are similarly regulated in response to candidate trans-acting factors. Importantly, CRISPR/CAS9-mediated deletion of the 3′ eye field/optic vesicle enhancer in X. laevis, resulted in a reduction in optic vesicle size. These results identify the cis-acting regions, demonstrate the modular nature of the elements controlling early versus late retinal expression, and identify potential regulators of six6 expression during the early stages of eye formation.
机译:眼场转录因子Six6对眼睛形成的早期阶段(规范和增殖生长)以及正常的视网膜祖细胞分化都是必不可少的。尽管已经描述了驱动视杯表达的基因组区域,但控制眼场和视泡表达的序列尚不清楚。确定了两个进化保守区5'和six6编码区的第三个3',并且它们一起忠实地复制了内源X. laevis six6表达模式。产生转基因品系,并用于确定由调节区控制的发作和表达模式。保守的3'区域对于眼场和视泡表达是必要的并且是足够的。相反,正常视杯和成熟视网膜表达需要一起位于编码序列5'的两个保守的增强子区域。功能获得性实验表明,F1转基因胚胎中的内源Six6和GFP表达对候选反式作用因子的响应受到类似调节。重要的是,CRISPR / CAS9介导的X.laevis中3'眼场/视泡增强子的缺失导致视泡大小的减小。这些结果确定了顺式作用区域,证明了控制视网膜早期和晚期视网膜表达的元件的模块性质,并确定了在眼睛形成早期阶段六六表达的潜在调节因子。

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