摘要
为开展β-防御素基因表达调控分子机制及其转基因防治粘膜感染的研究,作者克隆了大鼠β-防御素rBD-1 cDNA。从大鼠肾脏组织提取RNA,采用RT-PCR技术扩增大鼠β-防御素rBD-1cDNA,并重组到pGEM-T Easy 载体,经限制性内切酶谱分析和DNA序列测定,证实所克隆的cDNA片段为大鼠β-防御素rBD-1 cDNA。
This is a study aimed at the molecular mechanisms of β defensins gene expression and it's gene transfer experiments for preventing mucosal infection. A rat rBD 1 cDNA was cloned. The total RNA was isolated from rat kidney. The cDNA fragment was amplified by RT PCR with specific primers. The purified RT PCR product was cloned in pGEM T Easy vector. The results of restriction endonuclease pattern analysis of the recombinant plasmid, DNA sequencing, and aligning of the putative amino acid sequence with hBD 1 and mBD 1 demonstrated that rat β defensin rBD 1 gene was cloned successfully.
出处
《华西医科大学学报》
CAS
CSCD
1999年第4期357-359,共3页
Journal of West China University of Medical Sciences
基金
国家自然科学基金!(93670684
93670305)
霍英东青年基金
纽约中华医学会基金!(98-681)