Muscat G E, Rea S, Downes M
University of Queensland, Centre for Molecular and Cellular Biology, Ritchie Research Laboratories, St Lucia, Australia.
Nucleic Acids Res. 1995 Apr 25;23(8):1311-8. doi: 10.1093/nar/23.8.1311.
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-TF II during mammalian cell differentiation.
COUP - TF II是一种“孤儿类固醇受体”,它能结合多种AGGTCA重复序列,并抑制甲状腺激素(T3)和视黄酸依赖的反式激活;然而,对于其在哺乳动物细胞分化过程中的功能和/或发育作用却知之甚少。T3和视黄酸已被证明可通过激活肌肉特异性肌分化因子基因家族(肌分化因子、肌细胞生成素、myf - 5和MRF - 4)来促进终末肌肉分化。肌分化因子基因家族可以决定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,我们研究了COUP - TF II在肌肉分化过程中的表达及功能作用。增殖的C2C12成肌细胞表达COUP - TF II mRNA,当通过血清饥饿诱导细胞分化为有丝分裂后多核肌管时,该mRNA表达受到抑制。与COUP - TF II mRNA减少同时出现的是肌肉特异性mRNA(如肌细胞生成素、α - 肌动蛋白)。我们发现,大肠杆菌表达的全长和截短的COUP - TF II以序列特异性方式与肌分化因子和肌细胞生成素调节性HLH基因中的T3反应元件(TREs)[奥尔森(1992年)《发育生物学》第154卷,第261 - 272页]以及骨骼肌α - 肌动蛋白收缩蛋白基因中的TRE结合。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视黄酸X受体复合物与这些TRE的异二聚体结合。在小鼠C2C12成肌细胞中组成型过表达COUP - TF II cDNA会抑制肌分化因子mRNA的水平,并阻断肌细胞生成素mRNA的诱导,而组成型表达反义COUP - TF II cDNA则显著增加肌分化因子mRNA的稳态水平并超诱导肌细胞生成素mRNA。这些研究首次证明:(i)COUP - TF II通过对肌分化因子基因家族的直接作用,作为一种与生理相关的成肌拮抗调节因子发挥作用;(ii)直接证明了COUP - TF II在哺乳动物细胞分化过程中的发育作用。