Iwai S A, Nishina Y, Kosaka M, Sumi T, Doi T, Sakuda M, Nishimune Y
2nd Department of Oral Surgery, Dental Faculty, Osaka University, Japan.
In Vitro Cell Dev Biol Anim. 1995 Jun;31(6):462-6. doi: 10.1007/BF02634259.
Changes in Hox1.6 and c-jun gene expression were examined upon F9 cell differentiation that was induced by three independent methods: a drug treatment with retinoic acid (RA), that with sodium butyrate (NaB), and a genetic approach using the ts mutant. To obtain further information on the mechanism of teratocarcinoma cell differentiation we have examined the kinetics of the induction of Hox1.6 and c-jun mRNA whose gene products have been demonstrated to have specific roles in gene regulation. Expression of Hox1.6 mRNA was induced more rapidly than c-jun mRNA by all the above three inducing methods. Furthermore, protein synthesis was not required for the induction of Hox1.6 mRNA as well as of c-jun mRNA synthesis in all three methods. The data suggested that the transcriptional increase in the Hox1.6 mRNA was a primary response and could play an important role in F9 cell differentiation.
采用三种独立方法诱导F9细胞分化后,检测了Hox1.6和c-jun基因表达的变化:用视黄酸(RA)进行药物处理、用丁酸钠(NaB)进行药物处理以及使用ts突变体的遗传学方法。为了获得关于畸胎癌细胞分化机制的更多信息,我们检测了Hox1.6和c-jun mRNA诱导的动力学,其基因产物已被证明在基因调控中具有特定作用。通过上述三种诱导方法,Hox1.6 mRNA的表达比c-jun mRNA诱导得更快。此外,在所有三种方法中,Hox1.6 mRNA以及c-jun mRNA的合成诱导均不需要蛋白质合成。数据表明,Hox1.6 mRNA的转录增加是一种初级反应,可能在F9细胞分化中起重要作用。