Transcription factor EGR1 promotes differentiation of bovine skeletal muscle satellite cells by regulating MyoG gene expression

被引:52
作者
Zhang, WeiWei [1 ,2 ]
Tong, HuiLi [1 ]
Zhang, ZiHeng [1 ]
Shao, ShuLi [2 ]
Liu, Dan [1 ]
Li, ShuFeng [1 ]
Yan, YunQin [1 ]
机构
[1] Northeast Agr Univ, Lab Cell & Dev, 59 Mucai St, Harbin 150030, Heilongjiang, Peoples R China
[2] Qiqihar Univ, Dept Life Sci & Agroforestry, Qiqihar, Heilongjiang, Peoples R China
关键词
bovine skeletal muscle satellite cells; differentiation; EGR1; MyoG; SEQUENCE-SPECIFIC CONTROL; STEM-CELLS; MOLECULAR REGULATION; TARGET GENES; GROWTH; MECHANISMS; MYOGENESIS; C2C12; INFLAMMATION; ACTIVATION;
D O I
10.1002/jcp.25883
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The transcription factor, early growth response 1 (EGR1), has important roles in various cell types in response to different stimuli. EGR1 is thought to be involved in differentiation of bovine skeletal muscle-derived satellite cells (MDSCs); however, the precise effects of EGR1 on differentiation of MDSCs and its mechanism of action remain unknown. In the present study, a time course of EGR1 expression and the effects of EGR1 on MDSC differentiation were determined. The results demonstrated that the expression of EGR1 mRNA and protein increased significantly in differentiating MDSCs relative to that in proliferating cells. Over-expression of the EGR1 gene in MDSCs promoted their differentiation and inhibited proliferation. Conversely, knock-down of EGR1 inhibited differentiation of MDSCs and promoted their proliferation, indicating that EGR1 promotes MDSC differentiation. Moreover, over-expression of EGR1 in MDSCs increased the expression of MyoG mRNA and protein, whereas its knock-down had the opposite effect. Furthermore, ChIP-PCR analyses demonstrated that EGR1 could bind directly to its putative binding site within the promoter region of MyoG, and determination of ERG1 subcellular localization in MDSCs demonstrated that it could relocate to the nucleus, indicating MyoG is likely an EGR1 target gene whose expression is positively regulated by this transcription factor. In conclusion, EGR1 can promote MDSC differentiation through positive regulation of MyoG gene expression.
引用
收藏
页码:350 / 362
页数:13
相关论文
共 47 条
[1]   The transcription factor Egr1 is a direct regulator of multiple tumor suppressors including TGFβ1, PTEN, p53, and fibronectin [J].
Baron, V ;
Adamson, ED ;
Calogero, A ;
Ragona, G ;
Mercola, D .
CANCER GENE THERAPY, 2006, 13 (02) :115-124
[2]   Transcription factor TEAD4 regulates expression of Myogenin and the unfolded protein response genes during C2C12 cell differentiation [J].
Benhaddou, A. ;
Keime, C. ;
Ye, T. ;
Morlon, A. ;
Michel, I. ;
Jost, B. ;
Mengus, G. ;
Davidson, I. .
CELL DEATH AND DIFFERENTIATION, 2012, 19 (02) :220-231
[3]   Regulation of distinct stages of skeletal muscle differentiation by mitogen-activated protein kinases [J].
Bennett, AM ;
Tonks, NK .
SCIENCE, 1997, 278 (5341) :1288-1291
[4]   Time course and side-by-side analysis of mesodermal, pre-myogenic, myogenic and differentiated cell markers in the chicken model for skeletal muscle formation [J].
Berti, Federica ;
Nogueira, Julia Meireles ;
Woehrle, Svenja ;
Sobreira, Debora Rodrigues ;
Hawrot, Katarzyna ;
Dietrich, Susanne .
JOURNAL OF ANATOMY, 2015, 227 (03) :361-382
[5]   Transcriptional mechanisms regulating skeletal muscle differentiation, growth and homeostasis [J].
Braun, Thomas ;
Gautel, Mathias .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2011, 12 (06) :349-361
[6]   Cellular and molecular regulation of muscle regeneration [J].
Chargé, SBP ;
Rudnicki, MA .
PHYSIOLOGICAL REVIEWS, 2004, 84 (01) :209-238
[7]   SEPARABLE REGULATORY ELEMENTS GOVERNING MYOGENIN TRANSCRIPTION IN MOUSE EMBRYOGENESIS [J].
CHENG, TC ;
WALLACE, MC ;
MERLIE, JP ;
OLSON, EN .
SCIENCE, 1993, 261 (5118) :215-218
[8]   Target gene selectivity of the myogenic basic helix-loop-helix transcription factor myogenin in embryonic muscle [J].
Davie, Judith K. ;
Cho, Jang-Hyeon ;
Meadows, Eric ;
Flynn, Jesse M. ;
Knapp, Jennifer R. ;
Klein, William H. .
DEVELOPMENTAL BIOLOGY, 2007, 311 (02) :650-664
[9]   MyoD targets chromatin remodeling complexes to the myogenin locus prior to forming a stable DNA-bound complex [J].
de la Serna, IL ;
Ohkawa, Y ;
Berkes, CA ;
Bergstrom, DA ;
Dacwag, CS ;
Tapscott, SJ ;
Imbalzano, AN .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (10) :3997-4009
[10]  
Dedieu S, 2002, INT J DEV BIOL, V46, P235