• 1. Department of Cardiovascular Surgery,General Hospital of Jinan Military Region, Jinan 250031, P. R. China. E-mail: AH7056 @163. com;;
  • 2. Department of Cardiovascular Surgery, Shandong Province Hospital, .Jinan 250012, P.R. China;
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Objective To construct the expression short hairpin RNA (shRNA) targeting gene kir2. 1 in rat myocardial cells, named pEGFP6 kir2. 1, and to observe the effects on the expression of messenger RNA(mRNA) and protein of gene kir2. 1 as well as the changes of myocardial beating rates. Methods Five RNA interference (RNAi) sites targeting the rat kir2. 1 gene was selected, designed and synthesized five pairs of oligonucleotides fragments ,annealed them to double-strand, then cloned them into the vectors containing U6 promoter,obtained the vector expressing five aim genes. Rat myocardial cells were divided into three groups: Experimental group, negative plasmid control group and normal control group. Reverse transcription-polymerase chain reaction(RT PCR) and Western-blot were carried out to detect the expression of the mRNA and protein of gene kir2.1 and the beating rates of myocardial cells were observed after 72 h. Results The expression of mRNA and protein of gene kir2. 1 of experimental group were markedly lower than that of other two control groups after 72 h(P〈0.01). There was no statistically significant between two control groups. The beating rate in experimental group was much faster than other two control groups (P〈0.01), remained unchanged in both negative plasmid control group and normal control group. Conclusion Plasmid pEGFP6-kir2.1 could suppress the expression of the mRNA and protein of kir2.1 and increase the rat cardiac muscle cell beats.

Citation: LI Fandong,LEI Yinsheng,ZOU Chengwei,et al .. Effects of shRNA by Plasmid-Mediated RNA Interference on Protein kir2. 1 Expression and Beat Frequency in Rat Myocardial Cells. Chinese Journal of Clinical Thoracic and Cardiovascular Surgery, 2006, 13(1): 28-31. doi: Copy