CONSTITUTIVE EXPRESSION OF THE ORPHAN RECEPTOR, REV-ERBA-ALPHA, INHIBITS MUSCLE DIFFERENTIATION AND ABROGATES THE EXPRESSION OF THE MYOD GENE FAMILY

被引:84
作者
DOWNES, M
CAROZZI, AJ
MUSCAT, GEO
机构
关键词
D O I
10.1210/me.9.12.1666
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rev-erbA alpha is an orphan steroid receptor that is expressed in skeletal muscle. Rev-erbA alpha binds to single/tandem copies of an AGGTCA motif, is transcribed on the noncoding strand of the c-erbA-alpha gene locus, and is postulated to modulate the thyroid hormone (T-3) response. T-3 induces terminal muscle differentiation and regulates fiber type composition via direct activation of the muscle-specific myoD gene family (e.g. myoD, myogenin). The myoD gene family can direct the fate of mesodermal cell lineages and activate muscle differentiation. Hence we investigated the expression and physiological role of Rev-erbA alpha during myogenesis. We observed abundant levels of Rev-erbA alpha mRNA in dividing C2C12 myoblasts, which were suppressed when the cells differentiated into postmitotic multinucleated myotubes. This decrease in Rev-erbA alpha mRNA correlated with the appearance of muscle-specific mRNAs (e.g, myogenin and alpha-actin). Constitutive overexpression of full length Rev-erbA alpha cDNA in the myogenic cells completely abolished differentiation, suppressed myoD mRNA levels, and abrogated the induction of myogenin mRNA. We then demonstrated that 1) GAL4-Rev-erbA alpha chimeras that contain the 'AB' region and lack the 'E' region activated transcription of GAL4 response elements in the presence of 8-Br-cAMP and 2) the ligand-binding domain (LED) contains an active transcriptional silencer. Overexpression of Rev-erbA alpha(Delta AB) in myogenic cells had no impact on the ability of these cells to morphologically or biochemically differentiate. Furthermore, this orphan receptor 1) down-regulated thyroid hormone receptor (TR)/T-3 mediated transciptional activity from the myogenin promoter and thyroid hormone response element (TRE) and 2) disrupted TR homodimer and TR/retinoid X receptor (RXR) heterodimer formation on a number of TREs found in the myoD gene family. In conclusion, Rev-erbA alpha functions as a negative regulator of myogenesis by targeting the expression of the myoD gene family. The mechanism of action may involve inhibition of functional TR/RXR heterodimer formation on critical TREs and dominant trans-repression of gene expression.
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页码:1666 / 1678
页数:13
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