Reactivation of developmentally silenced globin genes through forced linear recruitment of remote enhancers.

IF 21 1区 医学 Q1 HEMATOLOGY
Blood Pub Date : 2025-06-02 DOI:10.1182/blood.2024028128
Anna-Karina Felder, Sjoerd J D Tjalsma, Han J M P Verhagen, Rezin Majied, Marjon J A M Verstegen, Thijs C J Verheul, Jeffrey van Haren, Rebecca Mohnani, Richard Gremmen, Peter H L Krijger, Sjaak Philipsen, Emile van den Akker, Wouter de Laat
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引用次数: 0

Abstract

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.

通过强制线性募集远程增强子来重新激活发育沉默的珠蛋白基因。
人类基因组包含调控DNA元件,增强子,可以在长染色体距离上激活基因转录。在这里,我们表明增强子距离可能是基因沉默的关键。我们证明,通过删除或倒置干预DNA序列,将正常远端强HBB增强子线性募集到发育沉默的胚胎HBE或胎儿HBG启动子,导致它们在成人红细胞和离体分化造血干细胞和祖细胞中强烈重新激活表达。在HBA位点上也有类似的观察结果,其中远端增强子的删除-招募强烈地重新激活胚胎HBZ表达。总的来说,我们的工作将功能分配给看似非调控的基因组片段:通过提供线性分离,它们可能支持基因自主控制其对远端增强子的转录反应。
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来源期刊
Blood
Blood 医学-血液学
CiteScore
23.60
自引率
3.90%
发文量
955
审稿时长
1 months
期刊介绍: Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.
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