Praja1 E3 ubiquitin ligase promotes skeletal myogenesis through degradation of EZH2 upon p38α activation

被引:43
作者
Consalvi, Silvia [1 ]
Brancaccio, Arianna [2 ,3 ]
Dall'Agnese, Alessandra [4 ]
Puri, Pier Lorenzo [1 ,4 ]
Palacios, Daniela [2 ]
机构
[1] IRCCS Fdn Santa Lucia, Lab Epigenet & Regenerat Pharmacol, Via Fosso Fiorano 64, I-00143 Rome, Italy
[2] IRCCS Fdn Santa Lucia, Lab Epigenet & Signal Transduct, Via Fosso Fiorano 64, I-00143 Rome, Italy
[3] Sapienza Univ, Dept Anat Histol Forens Med & Orthoped, Via Scarpa 14, I-00161 Rome, Italy
[4] Sanford Burnham Prebys Med Discovery Inst, Dev Aging & Regenerat Program, La Jolla, CA 92037 USA
关键词
MUSCLE STEM-CELLS; GENE-EXPRESSION; PROTEIN EZH2; COMPLEX; PHOSPHORYLATION; DIFFERENTIATION; MAPK; TRANSCRIPTION; PATHWAY; RHABDOMYOSARCOMA;
D O I
10.1038/ncomms13956
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polycomb proteins are critical chromatin modifiers that regulate stem cell differentiation via transcriptional repression. In skeletal muscle progenitors Enhancer of zeste homologue 2 (EZH2), the catalytic subunit of Polycomb Repressive Complex 2 (PRC2), contributes to maintain the chromatin of muscle genes in a repressive conformation, whereas its down-regulation allows the progression through the myogenic programme. Here, we show that p38 alpha kinase promotes EZH2 degradation in differentiating muscle cells through phosphorylation of threonine 372. Biochemical and genetic evidence demonstrates that the MYOD-induced E3 ubiquitin ligase Praja1 (PJA1) is involved in regulating EZH2 levels upon p38 alpha activation. EZH2 premature degradation in proliferating myoblasts is prevented by low levels of PJA1, its cytoplasmic localization and the lower activity towards unphosphorylated EZH2. Our results indicate that signal-dependent degradation of EZH2 is a prerequisite for satellite cells differentiation and identify PJA1 as a new player in the epigenetic control of muscle gene expression.
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页数:11
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