Characterization of an eye field-like state during optic vesicle organoid development

L. Owen, J. Rainger, Hemant Bengani, F. Kilanowski, David R FitzPatrick, A. Papanastasiou
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引用次数: 1

Abstract

Specification of the eye field (EF) within the neural plate marks the earliest detectable stage of eye development. Experimental evidence, primarily from non-mammalian model systems, indicates that the stable formation of this group of cells requires the activation of a set of key transcription factors (TFs). This critical event is challenging to probe in mammals and, quantitatively, little is known regarding the regulation of the transition of cells to this ocular fate. Using optic vesicle organoids to model the onset of the EF, we generate timecourse transcriptomic data allowing us to identify dynamic gene-expression programs that characterise this cellular-state transition. Integrating this with chromatin accessibility data suggests a direct role of canonical EFTFs in regulating these gene-expression changes, and high-lights candidate cis-regulatory elements through which these TFs act. Finally, we begin to test a subset of these candidate enhancer elements, within the organoid system, by perturbing the underlying DNA sequence and measuring transcriptomic changes during EF activation.
视神经囊泡类器官发育过程中视场样状态的表征
神经板内的视野(EF)的规格标志着眼睛发育的最早可检测阶段。主要来自非哺乳动物模型系统的实验证据表明,这组细胞的稳定形成需要激活一组关键转录因子(tf)。这一关键事件在哺乳动物中具有挑战性,并且在定量上,关于细胞向这种眼部命运转变的调节知之甚少。使用视神经囊泡类器官来模拟EF的发生,我们生成了时序转录组数据,使我们能够识别表征这种细胞状态转变的动态基因表达程序。将这些数据与染色质可及性数据相结合,表明典型eftf在调节这些基因表达变化中的直接作用,并突出了这些tf通过的候选顺式调控元件。最后,我们开始在类器官系统中通过干扰潜在的DNA序列和测量EF激活过程中的转录组变化来测试这些候选增强子元件的一个子集。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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