Felder Anna-Karina, Tjalsma Sjoerd J D, Verhagen Han J M P, Majied Rezin, Verstegen Marjon J A M, Verheul Thijs C J, van Haren Jeffrey, Mohnani Rebecca, Gremmen Richard, Krijger Peter H L, Philipsen Sjaak, van den Akker Emile, de Laat Wouter
Hubrecht, Utrecht, Netherlands.
Sanquin Research and Landsteiner Lab. AMC/UvA, Amsterdam, Netherlands.
Blood. 2025 Jun 2. doi: 10.1182/blood.2024028128.
The human genome contains regulatory DNA elements, enhancers, that can activate gene transcription over long chromosomal distances. Here, we show that enhancer distance can be critical for gene silencing. We demonstrate that linear recruitment of the normally distal strong HBB enhancer to developmentally silenced embryonic HBE or fetal HBG promoters, through deletion or inversion of intervening DNA sequences, results in their strongly reactivated expression in adult erythroid cells and ex vivo differentiated hematopoietic stem and progenitor cells. A similar observation is made in the HBA locus, where deletion-to-recruit of the distal enhancer strongly reactivates embryonic HBZ expression. Overall, our work assigns function to seemingly non-regulatory genomic segments: by providing linear separation they may support genes to autonomously control their transcriptional response to distal enhancers.
人类基因组包含调控性DNA元件,即增强子,其可在长染色体距离上激活基因转录。在此,我们表明增强子距离对于基因沉默可能至关重要。我们证明,通过缺失或颠倒中间DNA序列,将通常位于远端的强HBB增强子线性募集到发育沉默的胚胎HBE或胎儿HBG启动子上,会导致它们在成体红细胞以及体外分化的造血干细胞和祖细胞中强烈重新激活表达。在HBA基因座中也有类似观察结果,远端增强子的缺失募集强烈重新激活了胚胎HBZ的表达。总体而言,我们的工作赋予了看似非调控性的基因组片段功能:通过提供线性间隔,它们可能支持基因自主控制其对远端增强子的转录反应。