Auradé F, Pinset C, Chafey P, Gros F, Montarras D
Institut Pasteur, Department of Molecular Biology, Paris, France.
Differentiation. 1994 Feb;55(3):185-92. doi: 10.1046/j.1432-0436.1994.5530185.x.
Cells of the embryonic mesenchymal cell line C3H10T1/2 have revealed the potential that the four regulatory factors belonging to the MyoD family have to activate myogenesis. In the present study we have further investigated the myogenic phenotype of C3H10T1/2 cells stably transfected with either Myf5, MyoD, myogenin or MRF4 cDNAs. We have studied the influence of each transfected cDNA on expression of the four endogenous muscle regulatory genes and on the ability of these embryonic myogenic derivatives to express adult muscle genes. No trace of endogenous transcripts distinct from the exogenous one was found in any of the four converted populations at the myoblast stage. This indicates that cross-activation within the MyoD family does not occur at the myoblast stage in these cells. Similarly, evidence was obtained that auto- or cross-activation of the Myf5 gene occurs neither at the myoblast stage nor at the myotube stage and that no autoactivation of the MRF4 gene occurs. Our results together with previous observations indicate that in C3H10T1/2 myogenic derivatives: (1) Autoactivation at the myoblast stage is restricted to MyoD (2) Expression from each cDNA alone is sufficient to establish and maintain the myoblast phenotype (3) The endogenous Myf5 gene is not mobilized. We have also observed that endogenous transcripts for MyoD and myogenin begin to accumulate at the onset of differentiation in the four myogenic derivatives, whereas accumulation of endogenous MRF4 transcripts starts after myotubes have formed and occurs at a much lower level (100- to 500-fold lower) than in differentiated cultures of myosatellite cells.(ABSTRACT TRUNCATED AT 250 WORDS)
胚胎间充质细胞系C3H10T1/2的细胞已显示出属于MyoD家族的四种调节因子激活肌生成的潜力。在本研究中,我们进一步研究了稳定转染Myf5、MyoD、肌细胞生成素或MRF4 cDNA的C3H10T1/2细胞的肌生成表型。我们研究了每种转染的cDNA对四个内源性肌肉调节基因表达的影响,以及这些胚胎肌生成衍生物表达成体肌肉基因的能力。在成肌细胞阶段的四个转化群体中,均未发现与外源转录本不同的内源性转录本痕迹。这表明在这些细胞的成肌细胞阶段,MyoD家族内不会发生交叉激活。同样,有证据表明,Myf5基因在成肌细胞阶段和肌管阶段均不会发生自激活或交叉激活,且MRF4基因也不会发生自激活。我们的结果与先前的观察结果表明,在C3H10T1/2肌生成衍生物中:(1)成肌细胞阶段的自激活仅限于MyoD;(2)每个cDNA单独表达足以建立和维持成肌细胞表型;(3)内源性Myf5基因未被激活。我们还观察到,在四种肌生成衍生物中,MyoD和肌细胞生成素的内源性转录本在分化开始时开始积累,而内源性MRF4转录本在肌管形成后开始积累,且积累水平比肌卫星细胞分化培养物中的低得多(低100至500倍)。(摘要截短于250字)