The construction and identification of siRNA expression vector against hypoxia inducible factor -1α in vitro
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R-33

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    Abstract:

    OBJECTIVE: Previous studies have suggested that under hypoxic conditions hypoxia inducible factor-1α (HIF-1α) contributes to the progression of neonatal pulmonary hemorrhage (NPH) by increasing the expression of endothelin-1 (ET-1) gene. RNA interference (RNAi) refers to the process of sequence-specific post-transcriptional gene-silencing mediated by double-stranded RNA. This new gene-silencing technique has recently been shown to be a powerful approach for studying gene function. The aim of this study was to construct the small interfering RNA (siRNA) eukaryotic expression vectors specific to human HIF-1α gene (pSIREN-Shuttle HIF-1α siRNA)in order to observe its silencing effect on HIF-1α under hypoxic conditions. METHODS: Six potential siRNA target sites (a-f)specific to human HIF-1α gene were designed and synthesized to two complementary oligonucleotides (A-F) for each siRNA target site. Using a gene recombination technique, the recombinant expression vectors (A-F′) were constructed by cloning the double strands oligonucleotide into RNAi-Ready pSIREN vector. The recombinant vectors were then transfected into the cultured human umbilical vein endothelial cells (HUVECs). After 48 hrs of culture, the cells were treated with CoCl2 (100 μM) for 3 hrs. Expression of HIF-1α mRNA and protein was detected using RT-PCR and Western blot. ET-1 level in cell culture supernates was detected using ELISA. RESULTS: The recombinant HIF-1α siRNA eukaryotic expression vectors A′-F′respectively aiming at sites (a-f) were constructed successfully. Compared to the non-transfection group, liposome-mediated gene transfection of pSIREN-Shuttle HIF-1α siRNA expression vectors into HUVECs obviously down-regulated the mRNA and protein levels of HIF-1α, and partly decreased the ET-1 level in the B′and D′ transfection groups. CONCLUSIONS: The specific pSIREN-Shuttle HIF-1α siRNA expression vectors B′ and D′ aiming at b and d sites can inhibit the expression of HIF-1α, thus decreasing the level of its target gene ET-1. This may be helpful to study the relationship between HIF-1α and neonatal pulmonary hemorrhage in vivo in future.

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何柳芳, 陈克正. HIF-1α特异性RNA干扰表达载体的构建及体外效应研究[J].中国当代儿科杂志英文版,2008,10(1):60-64

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  • Online: September 08,2009
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