Paatela Ellen M, St Amant Faith G, Hamm Danielle C, Bennett Sean R, Gujral Taranjit S, van der Maarel Silvère M, Tapscott Stephen J
Human Biology Division, Fred Hutchinson Cancer Center, 1100 Fairview Ave N, Seattle, WA 98109, United States.
Molecular and Cellular Biology Graduate Program, University of Washington, 1705 NE Pacific St, Seattle, WA 98195, United States.
Hum Mol Genet. 2025 Sep 3;34(18):1526-1540. doi: 10.1093/hmg/ddaf114.
The DUX4 transcription factor is briefly expressed in the early embryo and is epigenetically repressed in somatic tissues. Loss of epigenetic repression can result in the aberrant expression of DUX4 in skeletal muscle and can cause facioscapulohumeral dystrophy (FSHD). Multiple factors have been identified as necessary to maintain epigenetic silencing of DUX4 in skeletal muscle, but whether specific sequences at the DUX4 locus are sufficient for initiating epigenetic silencing has not been known. We cloned fragments of the D4Z4 macrosatellite repeat, the DNA region that encompasses the DUX4 retrogene, adjacent to a reporter driven by a constitutive promoter and identified a single fragment sufficient to epigenetically repress reporter gene expression. Previously identified repressors of DUX4 expression-SETDB1, ATF7IP, SIN3A/B, and LRIF1-were necessary for silencing activity and p38 inhibitors enhanced suppression. These findings identify a key regulatory sequence for D4Z4 epigenetic repression and establish a model system for mechanistic and discovery studies.
DUX4转录因子在早期胚胎中短暂表达,并在体细胞组织中受到表观遗传抑制。表观遗传抑制的丧失会导致DUX4在骨骼肌中异常表达,并可引起面肩肱型肌营养不良症(FSHD)。已确定多种因素对于维持骨骼肌中DUX4的表观遗传沉默是必需的,但尚不清楚DUX4基因座处的特定序列是否足以启动表观遗传沉默。我们克隆了D4Z4大卫星重复序列的片段,该DNA区域包含DUX4反转录基因,与由组成型启动子驱动的报告基因相邻,并鉴定出一个足以表观遗传抑制报告基因表达的单一片段。先前鉴定的DUX4表达抑制剂——SETDB1、ATF7IP、SIN3A/B和LRIF1——对于沉默活性是必需的,并且p38抑制剂增强了抑制作用。这些发现确定了D4Z4表观遗传抑制的关键调控序列,并建立了一个用于机制和发现研究的模型系统。