Shimokawa T, Kato M, Ezaki O, Hashimoto S
Molecular Medicine Laboratories, Yamanouchi Pharmaceutical Co., Ltd., Ibaraki, Japan.
Biochem Biophys Res Commun. 1998 May 8;246(1):287-92. doi: 10.1006/bbrc.1998.8600.
A rapid, highly sensitive method to determine the mRNA level of muscle-specific markers using TaqMan PCR analysis was developed and used to study sequential gene regulation of myoblasts during induced differentiation of C2C12 cells. mRNA levels of muscle regulatory factor (MRF) myogenin, alpha-actin, thermoregulatory uncoupling protein UCP2 and glucose transporter isotype glut4 increased rapidly during early stage differentiation. In contrast, myf5, beta-actin, UCP1 and glut1 mRNA levels gradually decreased during 8 days. However, the mRNA level of other genes such as MyoD, glyceraldehyde-3-phosphate dehydrogenase and hexokinase II changed only slightly in comparison. Muscle-specific uncoupling protein UCP3 mRNA was detected during differentiation and increased rapidly within 8 days. These data clearly show the sequential and the differential regulation of muscle-specific genes in C2C12 cells during multinucleate myotube formation.
开发了一种使用TaqMan PCR分析来测定肌肉特异性标志物mRNA水平的快速、高度灵敏的方法,并用于研究C2C12细胞诱导分化过程中成肌细胞的顺序基因调控。在早期分化过程中,肌肉调节因子(MRF)肌细胞生成素、α-肌动蛋白、体温调节解偶联蛋白UCP2和葡萄糖转运蛋白异构体glut4的mRNA水平迅速增加。相比之下,在8天内myf5、β-肌动蛋白、UCP1和glut1的mRNA水平逐渐下降。然而,其他基因如MyoD、甘油醛-3-磷酸脱氢酶和己糖激酶II的mRNA水平相比之下变化很小。在分化过程中检测到肌肉特异性解偶联蛋白UCP3的mRNA,并在8天内迅速增加。这些数据清楚地表明了在多核肌管形成过程中C2C12细胞中肌肉特异性基因的顺序和差异调控。