番茄hp1和dg基因高效检测体系的建立
- 摘要:
- 根据NCBI中提供的番茄红素单碱基突变基因hp1和dg的序列,设计特异性引物。利用同一PCR反应体系同时扩增筛选番茄红素基因hp1和dg,以及野生型基因HP1和DG。结果表明:扩增的特异性片段与单基因引物扩增片段完全吻合。SNP分子标记为单显性标记,突变基因纯合体只在突变材料PCR体系中产生298和870bp的特异性片段,野生基因纯合体只在野生材料PCR体系中产生298和870bp的特异性片段,杂合体在2个反应体系中均有特异性片段。利用该体系在F2代中筛选出同时含hp1和dg基因的纯合植株,大大节省了工作量,提高了准确度。
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备注/Memo
基金:国家科技部“863”计划资助项目(2007AA10Z-178)