Gauthier-Rouviere C, Vandromme M, Tuil D, Lautredou N, Morris M, Soulez M, Kahn A, Fernandez A, Lamb N
Cell Biology Unit, Centre de Recherche de Macromoléculaire, CNRS-INSERM, Montpellier, France.
Mol Biol Cell. 1996 May;7(5):719-29. doi: 10.1091/mbc.7.5.719.
To understand the mechanism by which the serum response factor (SRF) is involved in the process of skeletal muscle differentiation, we have assessed the effect of inhibiting SRF activity or synthesis on the expression of the muscle-determining factor MyoD. Inhibition of SRF activity in mouse myogenic C2C12 cells through microinjection of either the SRE oligonucleotide (which acts by displacing SRF proteins from the endogenous SRE sequences), purified SRF-DB (a 30-kDa portion of SRF containing the DNA-binding domain of SRF, which acts as a dominant negative mutant in vivo), or purified anti-SRF antibodies rapidly prevents the expression of MyoD. Moreover, the rapid shutdown of MyoD expression after in vivo inhibition of SRF activity is observed not only in proliferating myoblasts but also in myoblasts cultured under differentiating conditions. Additionally, by using a cellular system expressing a glucocorticoid-inducible antisense-SRF (from aa 74 to 244) we have shown that blocking SRF expression by dexamethasone induction of antisense SRF results in the lack of MyoD expression as probed by both immunofluorescence and Northern blot analysis. Taken together these data demonstrate that SRF expression and activity are required for the expression of the muscle-determining factor MyoD.
为了解血清反应因子(SRF)参与骨骼肌分化过程的机制,我们评估了抑制SRF活性或合成对肌肉决定因子MyoD表达的影响。通过显微注射SRE寡核苷酸(通过从内源性SRE序列置换SRF蛋白起作用)、纯化的SRF-DB(SRF的一个30 kDa部分,包含SRF的DNA结合结构域,在体内作为显性负突变体起作用)或纯化的抗SRF抗体来抑制小鼠成肌C2C12细胞中的SRF活性,可迅速阻止MyoD的表达。此外,在体内抑制SRF活性后,MyoD表达的快速关闭不仅在增殖的成肌细胞中观察到,在分化条件下培养的成肌细胞中也观察到。此外,通过使用表达糖皮质激素诱导型反义SRF(从第74位氨基酸到第244位氨基酸)的细胞系统,我们表明,地塞米松诱导反义SRF阻断SRF表达会导致免疫荧光和Northern印迹分析均检测到MyoD表达缺失。这些数据综合起来表明,肌肉决定因子MyoD的表达需要SRF的表达和活性。