目的 用反轉(zhuǎn)錄PCR法,調(diào)取膽囊癌細(xì)胞內(nèi)的端粒酶RNA(hTR)基因,并針對(duì)其序列設(shè)計(jì)錘頭狀核酶切割基因序列,并將其構(gòu)建入真核表達(dá)載體pTriEx4內(nèi)。
方法 根據(jù)hTR cDNA序列,設(shè)計(jì)引物,經(jīng)RT-PCR法從體外培養(yǎng)的膽囊癌細(xì)胞內(nèi)調(diào)取hTR模板區(qū)基因,根據(jù)其測(cè)序結(jié)果,合成錘頭狀核酶基因,與經(jīng)相應(yīng)酶切的真核表達(dá)載體連接,酶切鑒定重組體的正確性。
結(jié)果 經(jīng)RT-PCR從細(xì)胞內(nèi)調(diào)出68 bp序列,與hTR cDNA比較,與模板區(qū)域堿基序列一致。核酶基因重組子經(jīng)酶切鑒定序列正確。
結(jié)論 RT-PCR法可調(diào)出膽囊癌hTR基因有效片段; 成功構(gòu)建了針對(duì)hTR模板區(qū)的核酶基因的真核表達(dá)載體,為膽囊癌的基因治療奠定了基礎(chǔ)。
引用本文: 靳斌,姜希宏,王學(xué)浩,張峰,王偉,劉賢錫. 膽囊癌hTR錘頭狀核酶基因真核表達(dá)載體的構(gòu)建. 中國(guó)普外基礎(chǔ)與臨床雜志, 2004, 11(5): 436-439. doi: 復(fù)制
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