Feng Qing, Snider Lauren, Jagannathan Sujatha, Tawil Rabi, van der Maarel Silvère M, Tapscott Stephen J, Bradley Robert K
Computational Biology Program, Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, United States.
Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, United States.
Elife. 2015 Jan 7;4:e04996. doi: 10.7554/eLife.04996.
Facioscapulohumeral muscular dystrophy (FSHD) is a muscular dystrophy caused by inefficient epigenetic repression of the D4Z4 macrosatellite array and somatic expression of the DUX4 retrogene. DUX4 is a double homeobox transcription factor that is normally expressed in the testis and causes apoptosis and FSHD when misexpressed in skeletal muscle. The mechanism(s) of DUX4 toxicity in muscle is incompletely understood. We report that DUX4-triggered proteolytic degradation of UPF1, a central component of the nonsense-mediated decay (NMD) machinery, is associated with profound NMD inhibition, resulting in global accumulation of RNAs normally degraded as NMD substrates. DUX4 mRNA is itself degraded by NMD, such that inhibition of NMD by DUX4 protein stabilizes DUX4 mRNA through a double-negative feedback loop in FSHD muscle cells. This feedback loop illustrates an unexpected mode of autoregulatory behavior of a transcription factor, is consistent with 'bursts' of DUX4 expression in FSHD muscle, and has implications for FSHD pathogenesis.
面肩肱型肌营养不良症(FSHD)是一种由D4Z4大卫星阵列的表观遗传抑制效率低下和DUX4反转录基因的体细胞表达引起的肌营养不良症。DUX4是一种双同源框转录因子,通常在睾丸中表达,当在骨骼肌中错误表达时会导致细胞凋亡和FSHD。DUX4在肌肉中的毒性机制尚未完全了解。我们报告称,DUX4引发的无义介导的mRNA降解(NMD)机制核心成分UPF1的蛋白水解降解与NMD的深度抑制有关,导致通常作为NMD底物被降解的RNA在整体上积累。DUX4 mRNA本身会被NMD降解,因此DUX4蛋白对NMD的抑制通过FSHD肌肉细胞中的双负反馈环使DUX4 mRNA稳定。这种反馈环说明了转录因子一种意想不到的自我调节行为模式,与FSHD肌肉中DUX4表达的“爆发”一致,并对FSHD发病机制具有重要意义。