Molina A, Iyengar A, Marins L F, Biemar F, Hanley S, Maclean N, Smith T J, Martial J A, Muller M
Laboratoire de Biologie Moléculaire et de Génie Génétique, Université de Liège, Institut de Chemie B6, Sart-Tilman, Belgium.
Biochim Biophys Acta. 2001 Sep 21;1520(3):195-202. doi: 10.1016/s0167-4781(01)00272-x.
We have cloned and characterized a tilapia (Oreochromis mossambicus) L18 ribosomal protein gene, including the complete transcribed region and 488 bp of upstream regulatory sequences. We have also isolated two L18 cDNAs from another tilapia (Oreochromis niloticus) with a few conservative nucleotide differences. Our results suggest the presence of two genes in both species. Reporter constructs were tested for transient expression in CV1 cells and in microinjected zebrafish and tilapia embryos. The tilapia L18 promoter was able to drive expression of the reporter gene in all three experiments, with no apparent preference for a particular tissue. The tilapia L18 promoter is therefore likely to be a powerful tool to drive tissue-independent gene expression in fish.
我们克隆并鉴定了罗非鱼(莫桑比克罗非鱼)的L18核糖体蛋白基因,包括完整的转录区域和488 bp的上游调控序列。我们还从另一种罗非鱼(尼罗罗非鱼)中分离出两个L18 cDNA,它们有一些保守的核苷酸差异。我们的结果表明这两个物种中都存在两个基因。对报告基因构建体进行了测试,以检测其在CV1细胞以及显微注射的斑马鱼和罗非鱼胚胎中的瞬时表达。罗非鱼L18启动子在所有这三个实验中都能够驱动报告基因的表达,对特定组织没有明显偏好。因此,罗非鱼L18启动子可能是在鱼类中驱动不依赖组织的基因表达的有力工具。