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

机译:不同的顺式代理区域控制眼场和眼部光学杯阶段的六号表达

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摘要

Abstract 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 F 1 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. Highlights ? Regulatory regions 5′ of the six6 gene drive optic cup and mature retinal expression. ? A 3′ regulatory region is sufficient for eye field and optic vesicle six6 expression. ? Several trans-acting factors that regulate endogenous six6 expression were identified. ? Deletion of the 3′ enhancer reduces eye size. ]]>
机译:摘要目前转录因子66对于眼球形成的早期(规格和增殖生长)阶段至关重要,以及正常的视网膜祖细胞分化。虽然已经描述了驱动S166光学杯表达的基因组区域,但控制眼场和光学囊泡表达的序列是未知的。鉴定了两个进化节保守区域5'和第三个3',并在一起,它们忠实地复制内源性X. Laevis Six6表达模式。产生转基因素并用于确定由调节区域控制的发作和表达模式。保守的3'区域是必要的,并且足以用于眼场和视光囊泡表达。相反,位于编码序列的5'的两个保守的增强子区域用于常视光杯和成熟的视网膜表达。函数实验表明F1转基因胚胎中的内源性S166和GFP表达在响应于候选反作用因子时类似地调节。重要的是,Crispr / Cas9介导的X.1Avis中的3'眼场/光学囊泡增强子缺失,导致光学囊泡尺寸的减少。这些结果鉴定了顺式作用区,证明了控制早期与晚视网膜表达的元素的模块化,并在眼层的早期阶段鉴定了S166表达的潜在调节因子。强调 ? Six6基因驱动光学杯和成熟视网膜表达的监管区域5'。还是对于眼场和光学囊泡的表达,3'调节区足以。还是确定了调节内源性六种表达的几种反式作用因子。还是删除3'增强剂可降低眼睛尺寸。 ]]>

著录项

  • 来源
    《Developmental biology》 |2017年第2期|共11页
  • 作者单位

    Department of Ophthalmology and The Center for Vision Research SUNY Upstate Medical University;

    Department of Ophthalmology and The Center for Vision Research SUNY Upstate Medical University;

    Department of Ophthalmology and The Center for Vision Research SUNY Upstate Medical University;

    Department of Ophthalmology and The Center for Vision Research SUNY Upstate Medical University;

    Department of Ophthalmology and The Center for Vision Research SUNY Upstate Medical University;

    Department of Ophthalmology and The Center for Vision Research SUNY Upstate Medical University;

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  • 正文语种 eng
  • 中图分类 生物学说;
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