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Prox1 增强子抑制脉管系统中的造血。

A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature.

机构信息

Centre for Cancer Biology, University of South Australia and SA Pathology, Adelaide, South Australia, Australia.

Department of Genetics and Molecular Pathology, SA Pathology, Adelaide, South Australia, Australia.

出版信息

Nature. 2023 Feb;614(7947):343-348. doi: 10.1038/s41586-022-05650-9. Epub 2023 Jan 25.

Abstract

Transcriptional enhancer elements are responsible for orchestrating the temporal and spatial control over gene expression that is crucial for programming cell identity during development. Here we describe a novel enhancer element that is important for regulating the expression of Prox1 in lymphatic endothelial cells. This evolutionarily conserved enhancer is bound by key lymphatic transcriptional regulators including GATA2, FOXC2, NFATC1 and PROX1. Genome editing of the enhancer to remove five nucleotides encompassing the GATA2-binding site resulted in perinatal death of homozygous mutant mice due to profound lymphatic vascular defects. Lymphatic endothelial cells in enhancer mutant mice exhibited reduced expression of genes characteristic of lymphatic endothelial cell identity and increased expression of genes characteristic of haemogenic endothelium, and acquired the capacity to generate haematopoietic cells. These data not only reveal a transcriptional enhancer element important for regulating Prox1 expression and lymphatic endothelial cell identity but also demonstrate that the lymphatic endothelium has haemogenic capacity, ordinarily repressed by Prox1.

摘要

转录增强子元件负责协调基因表达的时空控制,这对于在发育过程中编程细胞身份至关重要。在这里,我们描述了一个新的增强子元件,它对于调节淋巴管内皮细胞中 Prox1 的表达很重要。这个进化上保守的增强子被关键的淋巴管转录调节因子结合,包括 GATA2、FOXC2、NFATC1 和 PROX1。对增强子进行基因组编辑,去除包含 GATA2 结合位点的五个核苷酸,导致纯合突变小鼠在围产期因严重的淋巴管血管缺陷而死亡。增强子突变小鼠的淋巴管内皮细胞表现出特征性淋巴管内皮细胞特征的基因表达减少,以及特征性造血内皮细胞的基因表达增加,并获得了生成造血细胞的能力。这些数据不仅揭示了一个对调节 Prox1 表达和淋巴管内皮细胞特征很重要的转录增强子元件,还证明了淋巴管内皮细胞具有造血能力,通常被 Prox1 抑制。

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