目的:克隆人AITRL基因cDNA,同时对其序列进行分析。方法:采用RT-PCR方法,从人脐静脉内皮细胞株中获得AITRL基因的cDNA,克隆至pMD18-T载体,选择阳性克隆进行酶切鉴定和序列测定。结果:扩增得到的AITRL基因cDNA为534bp,编码177个氨基酸残基,与GenBank中公布的序列完全一致。结论:获得人AITRL基因的克隆,为进一步研究其生物学功能奠定了良好基础。
Objective: To clone and analyze a full-lenth cDNA encoding human activation-inducible tumor necrosis factor receptor ligand (AITRL) gene. Methods: The eDNA of AITRL was amplified by RTPCR using the total RNA extracted from human umbilical vein endothelial cell (HUVEC) . The PCR product was inserted into pMD18-T vector and then transformed into E. coli DH5α. The positive recombinant clone was analyzed by digestion of restriction endonuelease and DNA sequencing. Results: The eDNA of AITRL has an complete open reading frame with a length of 534 bp, which encodes a product of 177 amino acid, and shares 100 % homology with the sequence of mRNA for human AITRL in GenBank. Conclusion: The eDNA of human AITRL was cloned successfully, which posed a basis for further researching on its biological function.