Eli and Edythe Broad Center for Regenerative Medicine, Department of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, United States.
Elife. 2021 Jan 27;10:e63595. doi: 10.7554/eLife.63595.
The specification of cartilage requires Sox9, a transcription factor with broad roles for organogenesis outside the skeletal system. How Sox9 and other factors gain access to cartilage-specific cis-regulatory regions during skeletal development was unknown. By analyzing chromatin accessibility during the differentiation of neural crest cells into chondrocytes of the zebrafish head, we find that cartilage-associated chromatin accessibility is dynamically established. Cartilage-associated regions that become accessible after neural crest migration are co-enriched for Sox9 and Fox transcription factor binding motifs. In zebrafish lacking Foxc1 paralogs, we find a global decrease in chromatin accessibility in chondrocytes, consistent with a later loss of dorsal facial cartilages. Zebrafish transgenesis assays confirm that many of these Foxc1-dependent elements function as enhancers with region- and stage-specific activity in facial cartilages. These results show that Foxc1 promotes chondrogenesis in the face by establishing chromatin accessibility at a number of cartilage-associated gene enhancers.
软骨的形成需要 Sox9,这是一种转录因子,在骨骼系统之外的器官发生中具有广泛的作用。在骨骼发育过程中,Sox9 和其他因子如何获得软骨特异性顺式调控区域的访问权限尚不清楚。通过分析神经嵴细胞向斑马鱼头软骨细胞分化过程中的染色质可及性,我们发现软骨相关的染色质可及性是动态建立的。在神经嵴细胞迁移后变得可及的软骨相关区域富含 Sox9 和 Fox 转录因子结合基序。在缺乏 Foxc1 旁系同源物的斑马鱼中,我们发现软骨细胞中的染色质可及性全面降低,这与随后的背侧面部软骨缺失一致。斑马鱼转基因分析证实,这些 Foxc1 依赖的元件中的许多作为增强子发挥作用,在面部软骨中具有区域和阶段特异性活性。这些结果表明,Foxc1 通过在多个软骨相关基因增强子上建立染色质可及性,在面部促进软骨生成。