Regeneration Next, Duke University, Durham, NC 27710, USA.
Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Development. 2020 Jul 30;147(14):dev191262. doi: 10.1242/dev.191262.
To identify candidate tissue regeneration enhancer elements (TREEs) important for zebrafish fin regeneration, we performed ATAC-seq from bulk tissue or purified fibroblasts of uninjured and regenerating caudal fins. We identified tens of thousands of DNA regions from each sample type with dynamic accessibility during regeneration, and assigned these regions to proximal genes with corresponding expression changes by RNA-seq. To determine whether these profiles reveal bona fide TREEs, we tested the sufficiency and requirements of several sequences in stable transgenic lines and mutant lines with homozygous deletions. These experiments validated new non-coding regulatory sequences near induced and/or essential genes during fin regeneration, including , and , identifying distinct domains of directed expression for each confirmed TREE. Whereas deletion of the previously identified enhancer abolished detectable induction of the nearby gene during regeneration, deletions of enhancers linked to , and had no effect or partially reduced gene expression. Our study generates a new resource for dissecting the regulatory mechanisms of appendage generation and reveals a range of requirements for individual TREEs in control of regeneration programs.
为了鉴定对斑马鱼鳍再生重要的候选组织再生增强子元件(TREEs),我们对未受伤和正在再生的尾鳍的组织或纯化的成纤维细胞进行了 ATAC-seq 分析。我们从每个样本类型中鉴定出了数万个在再生过程中具有动态可及性的 DNA 区域,并通过 RNA-seq 将这些区域分配到具有相应表达变化的近端基因上。为了确定这些图谱是否揭示了真正的 TREEs,我们在稳定的转基因系和纯合缺失突变系中测试了几个序列的充分性和要求。这些实验验证了在鳍再生过程中诱导和/或必需基因附近的新的非编码调控序列,包括 、 和 ,为每个确认的 TREE 确定了定向表达的不同区域。虽然先前鉴定的 增强子的缺失消除了在再生过程中检测到的附近 基因的诱导,但与 、 和 相关的增强子的缺失没有影响或部分降低了基因表达。我们的研究为解析附肢生成的调控机制提供了一个新的资源,并揭示了个体 TREEs 在控制再生程序中的一系列要求。