Pinney D F, Pearson-White S H, Konieczny S F, Latham K E, Emerson C P
Department of Biology, University of Virginia, Charlottesville 22901.
Cell. 1988 Jun 3;53(5):781-93. doi: 10.1016/0092-8674(88)90095-5.
Stable myogenic cell lines have been derived at a high frequency by transfection of a cloned multipotential mouse embryo cell line, C3H 10T1/2, with cloned human DNA linked to a selectable neomycin resistance gene. The myogenic phenotype remains linked to neomycin resistance during secondary transfections. Although proliferative in growth conditions, these cell lines maintain the ability to differentiate and express muscle-specific proteins. We conclude that there is a simple genetic basis for myogenic determination and that a single gene, myd, converts 10T1/2 cells to a myoblast lineage. Southern blot analysis demonstrates nonidentity of myd and the MyoD1 gene. Northern blot analysis shows that myd-transfected myogenic lineages express MyoD1 mRNA while parental 10T1/2 cells do not. These results suggest that a dependent regulatory gene pathway mediates myogenic determination and differentiation.
通过将与可选择的新霉素抗性基因相连的克隆人类DNA转染到克隆的多能小鼠胚胎细胞系C3H 10T1/2中,已高频获得稳定的成肌细胞系。在二次转染过程中,成肌表型仍与新霉素抗性相关联。尽管这些细胞系在生长条件下具有增殖能力,但它们仍保持分化并表达肌肉特异性蛋白的能力。我们得出结论,成肌决定存在一个简单的遗传基础,并且一个单一基因myd可将10T1/2细胞转化为成肌细胞谱系。Southern印迹分析表明myd与MyoD1基因不同。Northern印迹分析显示,转染myd的成肌谱系表达MyoD1 mRNA,而亲本10T1/2细胞则不表达。这些结果表明,一个依赖的调节基因途径介导了成肌决定和分化。