Elder P K, French C L, Subramaniam M, Schmidt L J, Getz M J
Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota 55905.
Mol Cell Biol. 1988 Jan;8(1):480-5. doi: 10.1128/mcb.8.1.480-485.1988.
Hybridization to synthetic oligonucleotides representing conserved regions in the promoter and first intron of several vertebrate beta-actin genes was used to discriminate between what appears to be a single functional beta-actin gene and numerous pseudogenes in the mouse genome. Sequences derived from the 5' end of this gene were shown to confer serum-inducible expression upon a heterologous reporter gene when transfected into mouse fibroblasts. Moreover, these sequences rendered reporter gene expression superinducible by a combination of serum and cycloheximide. These experiments indicate that the 5' end of the mouse beta-actin gene contains sequence elements which mediate the stimulatory effects of serum growth factors and which are responsive to both positive and negative regulators of gene expression.
利用与几种脊椎动物β-肌动蛋白基因启动子和第一内含子保守区域的合成寡核苷酸杂交,来区分小鼠基因组中看似单一的功能性β-肌动蛋白基因和众多假基因。当转染到小鼠成纤维细胞中时,源自该基因5'端的序列可使异源报告基因获得血清诱导型表达。此外,这些序列使报告基因的表达在血清和环己酰亚胺的共同作用下超诱导。这些实验表明,小鼠β-肌动蛋白基因的5'端含有介导血清生长因子刺激作用且对基因表达的正负调节因子均有反应的序列元件。