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一个Sox2增强子簇调控小鼠胚胎干细胞的区域特异性神经命运。

A Sox2 enhancer cluster regulates region-specific neural fates from mouse embryonic stem cells.

作者信息

Tobias Ian C, Moorthy Sakthi D, Shchuka Virlana M, Langroudi Lida, Cherednychenko Mariia, Gillespie Zoe E, Duncan Andrew G, Tian Ruxiao, Gajewska Natalia A, Di Roberto Raphaël B, Mitchell Jennifer A

机构信息

Department of Cell and Systems Biology, University of Toronto, Toronto, Ontario M5S 3G5, Canada.

出版信息

G3 (Bethesda). 2025 Apr 17;15(4). doi: 10.1093/g3journal/jkaf012.

Abstract

Sex-determining region Y box 2 (Sox2) is a critical transcription factor for embryogenesis and neural stem and progenitor cell (NSPC) maintenance. While distal enhancers control Sox2 in embryonic stem cells (ESCs), enhancers closer to the gene are implicated in Sox2 transcriptional regulation in neural development. We hypothesize that a downstream enhancer cluster, termed Sox2 regulatory regions 2-18 (SRR2-18), regulates Sox2 transcription in neural stem cells and we investigate this in NSPCs derived from mouse ESCs. Using functional genomics and CRISPR-Cas9-mediated deletion analyses, we investigate the role of SRR2-18 in Sox2 regulation during neural differentiation. Transcriptome analyses demonstrate that the loss of even 1 copy of SRR2-18 disrupts the region-specific identity of NSPCs, reducing the expression of genes associated with more anterior regions of the embryonic nervous system. Homozygous deletion of this Sox2 neural enhancer cluster causes reduced SOX2 protein, less frequent interaction with transcriptional machinery, and leads to perturbed chromatin accessibility genome-wide further affecting the expression of neurodevelopmental and anterior-posterior regionalization genes. Furthermore, homozygous NSPC deletants exhibit self-renewal defects and impaired differentiation into cell types found in the brain. Altogether, our data define a cis-regulatory enhancer cluster controlling Sox2 transcription in NSPCs and highlight the sensitivity of neural differentiation processes to decreased Sox2 transcription, which causes differentiation into posterior neural fates, specifically the caudal neural tube. This study highlights the importance of precise Sox2 regulation by SRR2-18 in neural differentiation.

摘要

性别决定区Y框蛋白2(Sox2)是胚胎发育以及神经干细胞和祖细胞(NSPC)维持过程中的关键转录因子。虽然远端增强子在胚胎干细胞(ESC)中控制Sox2,但更靠近该基因的增强子与神经发育过程中Sox2的转录调控有关。我们假设一个称为Sox2调控区域2 - 18(SRR2 - 18)的下游增强子簇在神经干细胞中调节Sox2转录,并在源自小鼠ESC的NSPC中对此进行研究。使用功能基因组学和CRISPR - Cas9介导的缺失分析,我们研究了SRR2 -

18在神经分化过程中对Sox2调控的作用。转录组分析表明,即使SRR2 - 18缺失1个拷贝也会破坏NSPC的区域特异性特征,降低与胚胎神经系统更前部区域相关基因的表达。这个Sox2神经增强子簇的纯合缺失导致SOX2蛋白减少,与转录机制的相互作用频率降低,并导致全基因组染色质可及性受到干扰,进一步影响神经发育和前后区域化基因的表达。此外,纯合的NSPC缺失体表现出自我更新缺陷以及向大脑中发现的细胞类型分化受损。总之,我们的数据定义了一个顺式调控增强子簇,其控制NSPC中Sox2的转录,并突出了神经分化过程对Sox2转录降低的敏感性,这会导致向后神经命运分化,特别是尾神经管。这项研究强调了SRR2 - 18对Sox2进行精确调控在神经分化中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bfc/12005160/b8b4e697bace/jkaf012f1.jpg

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