McGuire Jimmy A, Cotoras Darko D, O'Connell Brendan, Lawalata Shobi Z S, Wang-Claypool Cynthia Y, Stubbs Alexander, Huang Xiaoting, Wogan Guinevere O U, Hykin Sarah M, Reilly Sean B, Bi Ke, Riyanto Awal, Arida Evy, Smith Lydia L, Milne Heather, Streicher Jeffrey W, Iskandar Djoko T
Museum of Vertebrate Zoology, University of California, Berkeley, CA, United States of America.
Department of Integrative Biology, University of California, Berkeley, CA, United States of America.
PeerJ. 2018 Mar 20;6:e4470. doi: 10.7717/peerj.4470. eCollection 2018.
We used Massively Parallel High-Throughput Sequencing to obtain genetic data from a 145-year old holotype specimen of the flying lizard, . Obtaining genetic data from this holotype was necessary to resolve an otherwise intractable taxonomic problem involving the status of this species relative to closely related sympatric species that cannot otherwise be distinguished from one another on the basis of museum specimens. Initial analyses suggested that the DNA present in the holotype sample was so degraded as to be unusable for sequencing. However, we used a specialized extraction procedure developed for highly degraded ancient DNA samples and MiSeq shotgun sequencing to obtain just enough low-coverage mitochondrial DNA (721 base pairs) to conclusively resolve the species status of the holotype as well as a second known specimen of this species. The holotype was prepared before the advent of formalin-fixation and therefore was most likely originally fixed with ethanol and never exposed to formalin. Whereas conventional wisdom suggests that formalin-fixed samples should be the most challenging for DNA sequencing, we propose that evaporation during long-term alcohol storage and consequent water-exposure may subject older ethanol-fixed museum specimens to hydrolytic damage. If so, this may pose an even greater challenge for sequencing efforts involving historical samples.
我们使用大规模平行高通量测序技术,从一只145岁的飞蜥全模式标本中获取遗传数据。从这个全模式标本中获取遗传数据,对于解决一个棘手的分类学问题是必要的,该问题涉及到这个物种相对于密切相关的同域物种的地位,而仅依据博物馆标本无法区分这些同域物种。初步分析表明,全模式标本样本中的DNA降解严重,无法用于测序。然而,我们使用了一种为高度降解的古代DNA样本开发的专门提取程序和MiSeq鸟枪法测序,获得了足够的低覆盖度线粒体DNA(721个碱基对),以最终确定全模式标本以及该物种的另一个已知标本的物种地位。全模式标本是在福尔马林固定法出现之前制备的,因此很可能最初是用乙醇固定的,从未接触过福尔马林。传统观点认为,福尔马林固定的样本对DNA测序来说应该是最具挑战性的,但我们认为,长期酒精储存期间的蒸发以及随之而来的接触水,可能会使年代较久的乙醇固定博物馆标本受到水解损伤。如果是这样,这可能会给涉及历史样本的测序工作带来更大的挑战。