Division of Neonatology and Pulmonary Biology, Perinatal Institute, Cincinnati Children's Research Foundation, Cincinnati, OH, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Nat Commun. 2024 Jun 19;15(1):5233. doi: 10.1038/s41467-024-49477-6.
Mutations in the FOXF1 gene, a key transcriptional regulator of pulmonary vascular development, cause Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins, a lethal lung disease affecting newborns and infants. Identification of new FOXF1 upstream regulatory elements is critical to explain why frequent non-coding FOXF1 deletions are linked to the disease. Herein, we use multiome single-nuclei RNA and ATAC sequencing of mouse and human patient lungs to identify four conserved endothelial and mesenchymal FOXF1 enhancers. We demonstrate that endothelial FOXF1 enhancers are autoactivated, whereas mesenchymal FOXF1 enhancers are regulated by EBF1 and GLI1. The cell-specificity of FOXF1 enhancers is validated by disrupting these enhancers in mouse embryonic stem cells using CRISPR/Cpf1 genome editing followed by lineage-tracing of mutant embryonic stem cells in mouse embryos using blastocyst complementation. This study resolves an important clinical question why frequent non-coding FOXF1 deletions that interfere with endothelial and mesenchymal enhancers can lead to the disease.
FOXF1 基因突变是肺血管发育的关键转录调节因子,可导致肺泡毛细血管发育不良伴肺静脉异位连接,这是一种影响新生儿和婴儿的致命肺部疾病。鉴定新的 FOXF1 上游调控元件对于解释为什么频繁的非编码 FOXF1 缺失与该疾病有关至关重要。在此,我们使用小鼠和人类患者肺的多组学单细胞 RNA 和 ATAC 测序来鉴定四个保守的内皮和成纤维细胞 FOXF1 增强子。我们证明内皮 FOXF1 增强子是自动激活的,而间充质 FOXF1 增强子受 EBF1 和 GLI1 调控。通过使用 CRISPR/Cpf1 基因组编辑在小鼠胚胎干细胞中破坏这些增强子,并使用胚胎嵌合体在小鼠胚胎中对突变胚胎干细胞进行谱系追踪,验证了 FOXF1 增强子的细胞特异性。这项研究解决了一个重要的临床问题,即为什么频繁的非编码 FOXF1 缺失干扰内皮和成纤维细胞增强子会导致疾病。