苔藓植物DNA条形码的初步研究——以气象科部分属为例

Z. Li
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引用次数: 4

摘要

我们比较了苔藓DNA条形码候选位点和用于扩增该位点的引物的性能。鉴定了叶绿体基因组3个编码位点(matK、rps4和rbcL-a)和4个非编码位点(atpB-rbcL、atbf - h、psbK-I和trnH-psbA)、线粒体基因组1个位点(nad5)和细胞核基因组1个位点(ITS2)的引物。本研究共筛选了雪蕨科5属14种74份样品。所有的matK引物和一对trnH-psbA引物失败。atpF-H和psbK-I引物的成功率较低。psbK-I的引物产生多个条带,atpF-H的PCR产物难以测序。对其余6个基因座的变异率、鉴定成功率和分辨率进行比较。结果表明,ITS2是最有希望用于苔藓类DNA条形码的候选序列。在叶绿体基因中,atpB-rbcL的分辨率最高。虽然trnH-psbA变化很大,但它太短,不能单独作为理想的条形码。用NJ法测定了叶绿体基因组合atpB-rbcL+trnH-psbA和rbcL-a++trnH-psbA的Ps均为64%。更多的基因座的添加并没有提高分辨率。所有这些基因座不存在条形码间隙。在进行DNA条形码鉴定之前进行了系统发育分析,但仍存在一些分类问题。这项研究证明了正确的物种划分和在植物DNA条形码中采用质体和核位点的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Preliminary Study on DNA Barcoding of Mosses——A Case of Part of Genera of Meteoriaceae
We compared the performances of the candidate loci for moss DNA barcoding and the primers used in amplifying the loci. Primers for three coded loci (matK,rps4 and rbcL-a) and four non-coded loci (atpB-rbcL,atpF-H,psbK-I and trnH-psbA) of the chloroplast genome,one from the mitochondrial genome (nad5),and one from the nucleus genome (ITS2) were evaluated. Seventy-four samples representing 14 species belonging to five genera of Trachypodoaceae (or Meteoriaceae) were screened. All primers for matK and a pair of primers for trnH-psbA failed. Low successes were encountered with the primers for atpF-H and psbK-I. The primers for psbK-I produced several bands and the PCR products of atpF-H were difficult to sequence. The powers of the remaining six loci were compared using the variability,identification success and the resolutions. It was found that ITS2 is the most promising candidate for DNA barcoding for mosses. Among the chloroplast genes,atpB-rbcL exhibited the highest resolution. Although trnH-psbA is very variable,it is too short to be an ideal barcode alone. Combinations of chloroplast genes were also tried and Ps of both atpB-rbcL+trnH-psbA and rbcL-a++trnH-psbA were 64% using NJ method. More additions of loci did not increase the resolution. No barcoding gap exists for all these loci. Phylogenetic analyses were carried out prior to the DNA barcoding evaluation and some taxonomic problems do exist. This study exemplifies the necessity of correct species delimitation and the adoption of both plastid and nuclear loci in plant DNA barcoding.
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