首页> 外文期刊>Nucleic Acids Research >Identification of a regulatory function for an orphan receptor in muscle: COUP-TF II affects the expression of the myoD gene family during myogenesis.
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Identification of a regulatory function for an orphan receptor in muscle: COUP-TF II affects the expression of the myoD gene family during myogenesis.

机译:鉴定肌肉中的孤儿受体的调节功能:COUP-TF II在成肌过程中影响myoD基因家族的表达。

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COUP-TF II is an 'orphan steroid receptor' that binds a wide variety of AGGTCA repeats and represses thyroid hormone (T3) and retinoid dependent trans-activation; however, very little is known of its functional and/or developmental role during mammalian cell differentiation. T3 and retinoids have been demonstrated to promote terminal muscle differentiation via activation of the muscle specific myoD gene family (myoD, myogenin, myf-5 and MRF-4). The myoD gene family can direct the fate of mesodermal cell lineages, repress proliferation, activate differentiation and the contractile phenotype. Hence, we investigated the expression and functional role of COUP-TF II during muscle differentiation. Proliferating C2C12 myoblasts expressed COUP-TF II mRNA which was repressed when cells were induced to differentiate into post-mitotic multinucleated myotubes by serum withdrawal. Concomitant with the decrease of COUP-TF II mRNA was the appearance of muscle specific mRNAs (e.g. myogenin, alpha-actin). We show that Escherichia coli expressed full length and truncated COUP-TF II bound in a sequence specific manner to the T3 response elements (TREs) in the myoD and myogenin regulatory HLH genes [Olson (1992) Dev. Biol. 154, 261-272]; and the TRE in the skeletal alpha-actin contractile protein gene. COUP-TF II diminished the homodimeric binding of the thyroid hormone receptor and the heterodimeric binding of thyroid hormone and retinoid X receptor complexes to these TREs. Constitutive over-expression of COUP-TF II cDNA in mouse C2C12 myogenic cells suppressed the levels of myoD mRNA and blocked the induction of myogenin mRNA, whereas constitutive expression of anti-sense COUP-TF II cDNA significantly increased the steady state levels of myoD mRNA and hyper-induced myogenin mRNA. These studies demonstrate for the first time (i) that COUP-TF II, functions as a physiologically relevant antagonistic regulator of myogenesis via direct effects on the myoD gene family and (ii) direct evidence for the developmental role of COUP-TFII during mammalian cell differentiation.
机译:COUP-TF II是一种“孤立类固醇受体”,可结合多种AGGTCA重复序列并抑制甲状腺激素(T3)和类视黄醇依赖性反式激活。然而,在哺乳动物细胞分化过程中其功能和/或发育作用知之甚少。已证明T3和类维生素A通过激活肌肉特异性myoD基因家族(myoD,myogenin,myf-5和MRF-4)来促进终末肌分化。 myoD基因家族可以指导中胚层细胞谱系的命运,抑制增殖,激活分化和收缩表型。因此,我们调查了COUP-TF II在肌肉分化过程中的表达和功能作用。增殖的C2C12成肌细胞表达COUP-TF II mRNA,当通过血清撤除诱导细胞分化为有丝分裂后的多核肌管时,其表达受到抑制。与COUP-TF II mRNA降低同时出现的是肌肉特异性mRNA(例如,肌生成素,α-肌动蛋白)。我们表明,大肠杆菌表达全长,并以序列特异性方式与myoD和肌生成素调节性HLH基因中的T3反应元件(TREs)结合而被截短的COUP-TF II [Olson(1992)Dev。生物学154,261-272];和骨骼肌α-肌动蛋白收缩蛋白基因中的TRE。 COUP-TF II减少了甲状腺激素受体的同二聚体结合以及甲状腺激素和类维生素X受体复合物与这些TRE的异二聚体结合。小鼠C2C12肌原性细胞中COUP-TF II cDNA的组成型过表达抑制了myoD mRNA的水平并阻止了肌成素mRNA的诱导,而反义COUP-TF II cDNA的组成性表达则显着增加了myoD mRNA的稳态水平和过度诱导的肌生成素mRNA。这些研究首次证明(i)COUP-TF II通过对myoD基因家族的直接作用,作为肌肉发生的生理相关拮抗调节剂,以及(ii)COUP-TFII在哺乳动物细胞中的发展作用的直接证据。差异化。

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