Qiu Lihua, Jiang Shigui, Zhou Falin, Zhang Dianchang, Huang Jianhua, Guo Yihui
Biotechnology and Aquiculture Laboratory, The South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 231 Xingangxi Road, Guangzhou, P.R. China.
Mol Biol Rep. 2008 Sep;35(3):431-8. doi: 10.1007/s11033-007-9103-5. Epub 2007 Jul 13.
The techniques of homology cloning and anchored PCR were used to clone the elongation factor 2 (EF-2) gene from black tiger shrimp (Penaeus monodon). The full length cDNA of black tiger shrimp EF-2 (btsEF-2) contained a 5' untranslated region (UTR) of 73 bp, an ORF of 2541 bp encoding a polypeptide of 846 amino acids with an estimated molecular mass of 95 kDa, and a 3( UTR of 112 bp. The searches for protein sequence similarities with BLAST analysis indicated that the deduced amino acid sequence of btsEF-2 was homological to the EF-2 of other species and even the mammalians. The conserved signature sequence of EF-2 gene family, GTPase effector domain and ADP-ribosylation domain were found in the btsEF-2 deduced amino acid sequence. The temporal expressions of gene in the different ovarian stages were measured by real time PCR. The mRNA expressions of the gene were constitutively expressed in ovary and different during the maturation stages. The result indicated that EF-2 gene was constitutively expressed and could play a critical role in the ovarian maturation stage.
采用同源克隆和锚定PCR技术从黑虎虾(斑节对虾)中克隆延伸因子2(EF-2)基因。黑虎虾EF-2(btsEF-2)的全长cDNA包含一个73 bp的5'非翻译区(UTR)、一个2541 bp的开放阅读框(ORF),编码一个由846个氨基酸组成的多肽,估计分子量为95 kDa,以及一个112 bp的3'UTR。通过BLAST分析搜索蛋白质序列相似性表明,btsEF-2推导的氨基酸序列与其他物种甚至哺乳动物的EF-2同源。在btsEF-2推导的氨基酸序列中发现了EF-2基因家族的保守特征序列、GTPase效应结构域和ADP-核糖基化结构域。通过实时PCR测定该基因在不同卵巢阶段的时序表达。该基因的mRNA表达在卵巢中组成性表达,在成熟阶段有所不同。结果表明,EF-2基因组成性表达,可能在卵巢成熟阶段发挥关键作用。