象草是热带和亚热带地区广泛栽培的多年生资源植物。为探讨华南象草4-香豆酸:CoA连接酶(4CL)基因下调表达对木质素合成的影响,本研究设计1对特异引物,PCR扩增获得一段长为374bp的干扰片段。通过TO-PO克隆,将该片段克隆到载体pCR/GW/TOPO,构建了入门克隆载体pENTR-4CL;再经过LR反应使pE-NTR-4CL上的干扰片段进入目的载体pCB2004B上,形成表达载体pCB2004B-4CL,最后通过冻融法将其转入到根癌农杆菌EHA105中。菌液PCR结果表明RNAi质粒已成功转入农杆菌,为进一步利用RNAi技术研究4CL基因的功能奠定了基础。
Pennisetum purpureum is a perennial resource plant and widely cultivated in tropical and sub-tropical regions.A pair of specific primers was designed to assess the effect of down-regulated expression of the 4-coumarate: CoA ligase(4CL) gene on lignin composition of P.purpureum cv.Huanan,using the 4CL gene sequence of P.purpureum cv.Mott(accession No: GU997597.1).An interference fragment of 374 bp was obtained by PCR amplification with the above primers and it was cloned into the pCR/GW/TOPO vector by TOPO cloning to obtain pENTER-4CL.The corresponding fragment on destination vector pCB2004B was then replaced by the interference fragment of pENTR-4CL by LR reaction to form the RNAi(RNA interference) expression vector pCB2004B-4CL.The Agrobacterium-mediated transformation of the expression vector was carried out using the freeze-thaw method,and the expected fragments appeared in the PCR products using bacterial liquid as a template.This study was a basis for research on the 4CL function of P.purpureum by RNAi technology.