Ding Zhen-Yu, Li Ze-Gui, Xing Yi-Zhan, Ji Hua, Li Hong-Li, Chang Zhi-Jie
Department of pharmacognosy, College of pharmacy, Third Military Medical University, Chongqing 400038, China.
Neurosci Bull. 2009 Jun;25(3):122-30. doi: 10.1007/s12264-009-8122-8.
To construct effective RNA-interference plasmids targeting mouse HIF-1alpha gene and testify their effects and specificities in interfering HIF-1alpha expression.
Three RNA-interference plasmids targeting mouse HIF-1alpha gene, pBS/U6/HIF-1alpha-siRNAI~III, were constructed and identified using double digestion method in the present study. RT-PCR, immunostaining and western blotting were employed to detect the expression alterations of HIF-1alpha in 293T cells following transfections of the three plasmids, respectively. The interference effect of pBS/U6/HIF1alphai-II in SH-SY5Y cell line was further investigated.
All the three RNA-interference plasmids, especially pBS/U6/HIF1alphai-II, showed significant inhibition in HIF-1alpha expression in 293T cell line. pBS/U6/HIF1alphai-II could also inhibit HIF-1alpha expression in SH-SY5Y cell line, in a dose-dependent way.
Plasmid pBS/U6/HIF1alphai-II constructed in our study can effectively and specifically inhibit HIF-1alpha expression, and its role in neural tube development and dysfunction will be further investigated. Construct of pBS/U6/HIF1alphai-II plasmid will provide a useful tool to study the role of HIF-1 pathway in embryogenesis, oncogenesis and ischemia development.
构建靶向小鼠低氧诱导因子-1α(HIF-1α)基因的有效RNA干扰质粒,并验证其对HIF-1α表达的干扰作用及特异性。
构建3种靶向小鼠HIF-1α基因的RNA干扰质粒pBS/U6/HIF-1α-siRNAI~III,采用双酶切法进行鉴定。分别转染这3种质粒后,运用RT-PCR、免疫染色及蛋白质印迹法检测293T细胞中HIF-1α的表达变化。进一步研究pBS/U6/HIF1αi-II对SH-SY5Y细胞系的干扰作用。
3种RNA干扰质粒,尤其是pBS/U6/HIF1αi-II,对293T细胞系中HIF-1α的表达均有显著抑制作用。pBS/U6/HIF1αi-II对SH-SY5Y细胞系中HIF-1α的表达也有抑制作用,且呈剂量依赖性。
本研究构建的质粒pBS/U6/HIF1αi-II可有效、特异性地抑制HIF-1α的表达,其在神经管发育及功能障碍中的作用将进一步研究。pBS/U6/HIF1αi-II质粒的构建为研究HIF-1通路在胚胎发生、肿瘤发生及缺血发展中的作用提供了有用工具。