Tanahashi H, Ito T, Inouye S, Tsuji F I, Sakaki Y
Research Laboratory for Genetic Information, Kyushu University, Fukuoka, Japan.
Gene. 1990 Dec 15;96(2):249-55. doi: 10.1016/0378-1119(90)90260-x.
Aequorin is a luminescent protein present in the jellyfish Aequoria victoria which emits light (at 460 nm) in the presence of Ca2+. We report here that aequorin can be used as a reporter enzyme to monitor gene expression in eukaryotic cells. A cDNA encoding apoaequorin was fused to several eukaryotic promoters, including those of SV40, RSV and the HSV-1 tk gene, and introduced into several cell lines such as CV-1, COS and HeLa. At appropriate times after transfection, the aequorin activities in cell extracts were measured by monitoring the intensity of light emitted at 460 nm when triggered by Ca2+ by the use of a photomultiplier photometer. The aequorin assay was shown to be as sensitive as the conventional CAT assay, and the relative activities of various promoters estimated by the aequorin assay were in general agreement with those obtained by the CAT assay. The aequorin assay can be done within 6-7 h from the preparation of extract to the measurement of activity without using radioactive compounds.
水母发光蛋白是一种存在于维多利亚多管发光水母中的发光蛋白,它在Ca2+存在的情况下会发出蓝光(波长460nm)。我们在此报告,水母发光蛋白可用作报告酶来监测真核细胞中的基因表达。编码脱辅基水母发光蛋白的cDNA与几种真核启动子融合,包括SV40、劳氏肉瘤病毒(RSV)和单纯疱疹病毒1型(HSV-1)胸苷激酶(tk)基因的启动子,并被导入几种细胞系,如CV-1、COS和HeLa细胞系。转染后的适当时间,通过使用光电倍增管光度计监测Ca2+触发时在460nm处发出的光强度,来测量细胞提取物中的水母发光蛋白活性。结果表明,水母发光蛋白检测法与传统的氯霉素乙酰转移酶(CAT)检测法一样灵敏,通过水母发光蛋白检测法估算的各种启动子的相对活性与通过CAT检测法获得的结果基本一致。从制备提取物到测量活性,水母发光蛋白检测法可在6-7小时内完成,且无需使用放射性化合物。