Tokunaga K, Takeda K, Kamiyama K, Kageyama H, Takenaga K, Sakiyama S
Division of Biochemistry, Chiba Cancer Center Research Institute, Japan.
Mol Cell Biol. 1988 Sep;8(9):3929-33. doi: 10.1128/mcb.8.9.3929-3933.1988.
We described the structures of mouse cytoskeletal gamma-actin cDNA clones and showed that there is strong conservation of the untranslated regions with human gamma-actin cDNA. In addition, we found that the expression levels of beta- and gamma-actin mRNAs are differentially controlled in various mouse tissues and cell types but are coordinately increased in the cellular growing state. These results suggest that there are multiple regulatory mechanisms of cytoskeletal actin genes and are consistent with the argument that beta- and gamma-actins might have functional diversity in mammalian cells.
我们描述了小鼠细胞骨架γ-肌动蛋白cDNA克隆的结构,并表明其非翻译区与人类γ-肌动蛋白cDNA有很强的保守性。此外,我们发现β-和γ-肌动蛋白mRNA的表达水平在不同的小鼠组织和细胞类型中受到差异调控,但在细胞生长状态下会协同增加。这些结果表明细胞骨架肌动蛋白基因存在多种调控机制,并且与β-和γ-肌动蛋白在哺乳动物细胞中可能具有功能多样性的观点一致。