Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Dev Cell. 2024 Mar 11;59(5):676-691.e5. doi: 10.1016/j.devcel.2024.01.004. Epub 2024 Jan 29.
Regeneration involves gene expression changes explained in part by context-dependent recruitment of transcriptional activators to distal enhancers. Silencers that engage repressive transcriptional complexes are less studied than enhancers and more technically challenging to validate, but they potentially have profound biological importance for regeneration. Here, we identified candidate silencers through a screening process that examined the ability of DNA sequences to limit injury-induced gene expression in larval zebrafish after fin amputation. A short sequence (s1) on chromosome 5 near several genes that reduce expression during adult fin regeneration could suppress promoter activity in stable transgenic lines and diminish nearby gene expression in knockin lines. High-resolution analysis of chromatin organization identified physical associations of s1 with gene promoters occurring preferentially during fin regeneration, and genomic deletion of s1 elevated the expression of these genes after fin amputation. Our study provides methods to identify "tissue regeneration silencer elements" (TRSEs) with the potential to reduce unnecessary or deleterious gene expression during regeneration.
再生涉及基因表达的变化,部分原因是转录激活因子在特定环境下募集到远端增强子。与增强子相比,沉默子与抑制性转录复合物的结合研究较少,而且在技术上更具挑战性,难以验证,但它们对再生具有深远的生物学意义。在这里,我们通过筛选过程鉴定了候选沉默子,该过程检查了 DNA 序列在斑马鱼幼虫鳍切除后限制损伤诱导的基因表达的能力。染色体 5 上靠近几个在成年鳍再生过程中降低表达的基因的一个短序列(s1)可以抑制稳定转基因系中的启动子活性,并减少敲入系中附近基因的表达。染色质组织的高分辨率分析确定了 s1 与基因启动子之间的物理关联,这种关联在鳍再生过程中更倾向于发生,并且 s1 的基因组缺失会在鳍切除后提高这些基因的表达。我们的研究提供了鉴定“组织再生沉默子元件”(TRSEs)的方法,这些元件有可能在再生过程中降低不必要或有害的基因表达。