Buck G A, Fox J W, Gunthorpe M, Hager K M, Naeve C W, Pon R T, Adams P S, Rush J
Virginia Commonwealth University, Richmond, USA.
Biotechniques. 1999 Sep;27(3):528-36. doi: 10.2144/99273rr01.
This study surveyed strategies of sequencing primer selection and evaluated primer performance in automated DNA sequencing. We asked participants to relate their preferred primer design strategies to identify primer characteristics that are considered most important in sequencing primer design. The participants preferred primers of 18-24 nucleotides (nt), 39%-58% G + C, a melting temperature (Tm) of 53 degrees-65 degrees C with a 1-2 nt 3' GC clamp, hairpin stems of less than 2-3 bp, homopolymeric runs of less than 4-5 nt, primer dimers of less than 3-4 bp and secondary priming sites of less than 3-4 bp. We provided a 300-bp test sequence and asked participants to submit sequences of 1-3 optimal sequencing primers. Submitted primers ranged from 17-24 nt and largely conformed to the preferred parameters. Submitted primers were distributed across the test sequence, although some sites were disfavored. Surprisingly, approximately 45% of the primers were selected "manually", more than by any software package. Each of 69 submitted and 95 control primers, distributed at 3-bp intervals across the test sequence, were synthesized, purified and tested using a Model 377 PRISM DNA Sequencer with dichlororhodamine dye terminator reagents (dRhodamine dye terminators). Approximately half of the control primers were also tested using rhodamine dye terminator reagents ("old" rhodamine dye terminators). The results indicated that primer physico-chemical characteristics thought to have a strong impact on sequencing performance had surprisingly little effect. Thus, primers with high or low percent G + C or Tm, strong secondary priming scores or long 3' homopolymeric stretches yielded excellent sequences with the dRhodamine dye terminator reagents, although these characteristics had a stronger effect when the old rhodamine reagents were used. The old rhodamine reagents gave sequences with a similar average read length, but the number of errors and ambiguities or "N's" was consistently higher. Moreover, the effects of the primer physico-chemical characteristics were also more evident with the old rhodamine dyes. We conclude that under optimal sequencing conditions with highly pure template and primer, many of the commonly applied primer design parameters are dispensable, particularly when using one of the new generation of sequencing reagents such as the dichlororhodamine dye terminators.
本研究调查了测序引物选择策略,并评估了自动DNA测序中引物的性能。我们要求参与者阐述他们偏爱的引物设计策略,以确定在测序引物设计中被认为最重要的引物特征。参与者偏爱18 - 24个核苷酸(nt)、G + C含量为39% - 58%、熔解温度(Tm)为53摄氏度 - 65摄氏度且带有1 - 2个nt 3' GC钳、发夹茎小于2 - 3 bp、同聚物连续长度小于4 - 5 nt、引物二聚体小于3 - 4 bp以及二级引物位点小于3 - 4 bp的引物。我们提供了一个300 bp的测试序列,并要求参与者提交1 - 3条最佳测序引物的序列。提交的引物长度在17 - 24 nt之间,并且在很大程度上符合偏爱参数。提交的引物分布在测试序列上,尽管有些位点不太受青睐。令人惊讶的是,大约45%的引物是“手动”选择的,比任何软件包选择的都多。在测试序列上以3 bp间隔分布的69条提交引物和95条对照引物,每条都使用带有二氯罗丹明染料终止剂试剂(dRhodamine染料终止剂)的377型PRISM DNA测序仪进行了合成、纯化和测试。大约一半的对照引物也使用罗丹明染料终止剂试剂(‘旧’罗丹明染料终止剂)进行了测试。结果表明,那些被认为对测序性能有强烈影响的引物物理化学特征,其影响出人意料地小。因此,G + C百分比或Tm值高或低、二级引物得分高或3' 同聚物延伸长的引物,使用dRhodamine染料终止剂试剂能产生出色的序列,不过当使用旧的罗丹明试剂时,这些特征的影响更强。旧的罗丹明试剂产生的序列平均读长相似,但错误和模糊碱基或‘N’的数量一直更高。此外,引物物理化学特征的影响在旧的罗丹明染料中也更明显。我们得出结论,在使用高纯度模板和引物的最佳测序条件下,许多常用的引物设计参数是不必要的,特别是在使用新一代测序试剂如二氯罗丹明染料终止剂时。