A feedback loop between nonsense-mediated decay and the retrogene DUX4 in facioscapulohumeral muscular dystrophy

被引:91
作者
Feng, Qing [1 ,2 ]
Snider, Lauren [3 ]
Jagannathan, Sujatha [1 ,2 ,3 ]
Tawil, Rabi [4 ]
van der Maarel, Silvere M. [5 ]
Tapscott, Stephen J. [3 ,6 ]
Bradley, Robert K. [1 ,2 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Computat Biol Program, Seattle, WA 98104 USA
[2] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
[3] Fred Hutchinson Canc Res Ctr, Human Biol Div, Seattle, WA 98104 USA
[4] Univ Rochester, Dept Neurol, Rochester, NY USA
[5] Leiden Univ, Med Ctr, Dept Human Genet, Leiden, Netherlands
[6] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
来源
ELIFE | 2015年 / 4卷
关键词
DUX4; facioscapulohumeral muscular dystrophy; FSHD; nonsense-mediated decay; MESSENGER-RNA; GENES; TRANSLATION; INHIBITION; PATIENT; LOCUS; MODEL;
D O I
10.7554/eLife.04996
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 mis-expressed 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.
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页数:25
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