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Identification of chloroplast DNA variations by PCR-RFLP analysis in Dendranthema

机译:通过PCR-RFLP分析鉴定树皮中的叶绿体DNA变异

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Variations in chloroplast DNA of Dendranthema species were studied by PCR-RFLP analysis to seel, the maternal origin of the cultivated chrysanthemum, D. grandiflorum. Ten genes, atpH, matK, petA, petB, psaA, rbcL, rpoB, rpoC, trnK and 16S in the chloroplast DNA of 12 Japanese wild species and 1 cultivar were amplified by PCR. The amplified DNAs that were digested with each of 32 restriction endonucleases revealed 13 site changes among the 13 species in the following 9 gene plus restriction endonuclease combinations: petA-AvaII, petA-HaeIII, petA-Mboll, petA-NdeII, rpoC-EcoRV, trnK-DraI, trnK-HinfI, trnK-MboII and trnK-ScrFI. No Japanese wild species showed the same PCR-RFLP pattern of chloroplast DNA as D. grandiflorum.
机译:通过PCR-RFLP分析研究了Dendranthema种的叶绿体DNA的变异,发现其为栽培菊花D. grandiflorum的母本。通过PCR扩增了12个日本野生种和1个品种的叶绿体DNA中的10个基因,分别为atpH,matK,petA,petB,psaA,rbcL,rpoB,rpoC,trnK和16S。用32种限制性内切核酸酶中的每一种消化的扩增DNA揭示了以下9个基因加限制性内切酶组合中的13种物种中的13个位点变化: trnK-DraI,trnK-HinfI,trnK-MboII和trnK-ScrFI。没有日本野生物种显示出与大叶杜鹃一样的叶绿体DNA PCR-RFLP模式。

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