DNA Barcoding in a Crop Genebank: The Capsicum annuum Species Complex

R. Jarret
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引用次数: 26

Abstract

Variability within eight cpDNA introns including trnS-trnfM, trnL-trnT, trnH-psbA, trnF-trnL, trnD-trnT, trnC- rpoB, rps16 and matK, and the nuclear waxy introns was examined in seven species of Capsicum (C. annuum, C. baccatum, C. chinense, C. frutescens, C. pubescens, C. chacoense and C. rhomboideum) in order to evaluate the feasibility of utilizing these loci for DNA barcoding within the C. annuum complex. Numerous insertions/deletions (indels) and substitutions were detected in all cpDNA introns. However, none was sufficient to differentiate the individual members of the C. annuum complex (C. annuum, C. chinense and C. frutescens). Variation within trnL-trnT, trnF-trnL and trnH-psbA enabled the differentiation of the complex from the other taxa examined. In contrast, single base indels and substitutions within the waxy introns permitted the differentiation of all taxa within the plant materials examined. The use of trnH-psbA or trnL-trnT, and the waxy introns is proposed for barcoding members of the C. annuum complex.
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作物基因库中的DNA条形码:辣椒物种复合体
研究了7种辣椒(C. annuum、C. bacaccatum、C. chinense、C. frutescens、C. pubescens、C. chacoense和C. rhomboideum)中8个cpDNA内含子(trns - trnm、trl - trnt、trnH-psbA、trnF-trnL、trnD-trnT、trnC- rpoB、rps16和matK)和核蜡质内含子的变异,以评价利用这些基因座进行辣椒复合体DNA条形码的可行性。在所有cpDNA内含子中检测到大量的插入/缺失(indel)和替换。然而,没有任何一种方法足以区分C. annuum复合体的单个成员(C. annuum, C. chinense和C. frutescens)。trnL-trnT、trnF-trnL和trnH-psbA内部的变异使该复合体与所研究的其他类群发生分化。相比之下,蜡质内含子内的单碱基索引和替换允许在所检查的植物材料中所有分类群的分化。建议使用trnH-psbA或trnL-trnT和蜡状内含子对C. annuum配合物的成员进行条形码。
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