Department of Cell Biology, Erasmus University Medical Center, Rotterdam, CN 3015, The Netherlands.
Center for Biomics, Erasmus University Medical Center, Rotterdam, CN 3015, The Netherlands.
Hum Mol Genet. 2020 Aug 29;29(15):2535-2550. doi: 10.1093/hmg/ddaa141.
The transcription factor zinc finger E-box binding protein 2 (ZEB2) controls embryonic and adult cell fate decisions and cellular maturation in many stem/progenitor cell types. Defects in these processes in specific cell types underlie several aspects of Mowat-Wilson syndrome (MOWS), which is caused by ZEB2 haplo-insufficiency. Human ZEB2, like mouse Zeb2, is located on chromosome 2 downstream of a ±3.5 Mb-long gene-desert, lacking any protein-coding gene. Using temporal targeted chromatin capture (T2C), we show major chromatin structural changes based on mapping in-cis proximities between the ZEB2 promoter and this gene desert during neural differentiation of human-induced pluripotent stem cells, including at early neuroprogenitor cell (NPC)/rosette state, where ZEB2 mRNA levels increase significantly. Combining T2C with histone-3 acetylation mapping, we identified three novel candidate enhancers about 500 kb upstream of the ZEB2 transcription start site. Functional luciferase-based assays in heterologous cells and NPCs reveal co-operation between these three enhancers. This study is the first to document in-cis Regulatory Elements located in ZEB2's gene desert. The results further show the usability of T2C for future studies of ZEB2 REs in differentiation and maturation of multiple cell types and the molecular characterization of newly identified MOWS patients that lack mutations in ZEB2 protein-coding exons.
转录因子锌指 E 盒结合蛋白 2(ZEB2)控制胚胎和成人细胞命运决定和许多干细胞/祖细胞类型中的细胞成熟。特定细胞类型中这些过程的缺陷是莫瓦特-威尔逊综合征(MOWS)的几个方面的基础,MOWS 是由 ZEB2 杂合不足引起的。人类 ZEB2 与小鼠 Zeb2 一样,位于 2 号染色体上,在一个约 3.5Mb 长的基因荒漠下游,缺乏任何编码蛋白的基因。使用时间靶向染色质捕获(T2C),我们在人类诱导多能干细胞的神经分化过程中显示了主要的染色质结构变化,基于 ZEB2 启动子与该基因荒漠之间的顺式接近性作图,包括在早期神经祖细胞(NPC)/玫瑰花结状态下,ZEB2 mRNA 水平显著增加。将 T2C 与组蛋白-3 乙酰化作图相结合,我们在 ZEB2 转录起始位点上游约 500kb 处鉴定了三个新的候选增强子。在异源细胞和 NPC 中的功能性荧光素酶测定显示这三个增强子之间的合作。这项研究首次记录了位于 ZEB2 基因荒漠内的顺式调控元件。结果进一步表明,T2C 可用于未来研究 ZEB2 在多种细胞类型的分化和成熟过程中的 REs,以及对缺乏 ZEB2 蛋白编码外显子突变的新确定的 MOWS 患者的分子特征进行研究。