抑制聚ADP核糖聚合酶1活性的短发夹RNA载体构建

目的构建抑制人聚ADP核糖聚合酶1(hPARP1)活性的短发夹RNA(shorthairpinRNA,shRNA)表达载体。方法化学合成2对编码短发夹RNA序列的、靶向hPARP1基因的寡核苷酸,各69对碱基,退火,然后利用BamHⅡ及EcoRⅠ与pSIRENRetroQ载体连接。用EcoRⅠ及BglⅡ切取其中U6启动子及下游的shRNA部分,与pEGFPC1载体重组构建pEGFPC1shRNA载体。结果重组构建的pEGFPC1P1、pEGFPC1P2、pEGFPC1N载体经双酶切电泳分析及插入基因片段序列分析,结果表明330个碱基成功插入到预计位点。结论载体的成功构建,为进一步研究聚ADP核糖聚合酶在DNA修复过程中的功能打下基础。

Construction of short hairpin RNA vector of inhibiting poly ADP-ribor polymerase activity

OBJECTIVE: To construct expressing vector of short hairpin RNA (shRNA) in order to inhibit human PARP1 activity. METHODS: 2 pairs of 64 base oligos for hairpin RNA expression which targeted PARP1 gene were chemically synthesized and annealed then ligased with pSIREN-RetroQ vector with BamH II and EcoR I . Cut by EcoR t and Bgl II, shRNA and its upstream U6, which have 330 bp, were inserted into the same treated pEGFP-C1 vecter to construct GFP expression plasmids that inhibited hPARPI protein shRNA plasmid (pEGFP-C1P). Oligos with a scrambled sequence were used as a negative control. RESULTS: Recombinant pEGFP-C1P1, pEGFP-C1P2 and pEGFP-C1N vectors was identified by digestion with EcoR I and Bgl II and confirmed by sequencing analysis with U6 primer. The results demonstrated that the 330 bp had been inserted into the expected site. Furthermore, the insertion sequence was exactly correct. CONCLUSION: pEGFP-C1-shRNA system has been constructed successfully. This will facilitate the study of PARP1's DNA repairing function.