a Departamento de Vertebrados, Museu Nacional, Universidade Federal do Rio de Janeiro, Quinta da Boa Vista, 20940-040 Rio de Janeiro, RJ, Brazil.
b Laboratório de Genômica e Biodiversidade, Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, 21941-902, Rio de Janeiro, RJ, Brazil.
Genome. 2019 Feb;62(2):77-83. doi: 10.1139/gen-2018-0145. Epub 2019 Feb 7.
Designing primers for DNA barcoding is a significant challenge for the rich Neotropical fish fauna, which is comprised of ∼6000 species. Previously, researchers required multiple pairs of PCR primers or primer cocktails to obtain standard COI (i.e., mitochondrial cytochrome c oxidase subunit I) barcode sequences from assemblages of freshwater fish in this region. To simplify DNA barcoding and metabarcoding studies of Neotropical freshwater fish, we present a new pair of COI primers, which have yielded high quality barcodes across six teleost orders-Characiformes, Cichliformes, Cyprinodontiformes, Gymnotiformes, Siluriformes, and Synbranchiformes-native to South America. Following previous fish barcoding studies, we also tailed our primers with M13 forward and reverse primers to facilitate the DNA sequencing process. Although this practice generates primer dimers, we obtained complete and high quality COI barcode sequences for all samples. We discuss the problem of primer dimers and suggest strategies for neutralizing their influence on data quality.
为 DNA 条形码设计引物是一个巨大的挑战,因为新热带鱼类区系拥有约 6000 种鱼类。此前,研究人员需要多对 PCR 引物或引物混合物才能从该地区的淡水鱼类组合中获得标准 COI(即线粒体细胞色素 c 氧化酶亚基 I)条形码序列。为了简化新热带淡水鱼类的 DNA 条形码和代谢条形码研究,我们提出了一对新的 COI 引物,该引物在原产于南美洲的六个硬骨鱼目(包括鲤形目、慈鲷目、脂鲤目、电鳗目、鲶形目和合鳃目)中产生了高质量的条形码。与之前的鱼类条形码研究一样,我们在引物的 M13 正向和反向引物上添加了尾巴,以方便 DNA 测序过程。尽管这种做法会产生引物二聚体,但我们为所有样本都获得了完整且高质量的 COI 条形码序列。我们讨论了引物二聚体的问题,并提出了一些策略来中和它们对数据质量的影响。