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Successful Recovery of Nuclear Protein-Coding Genes from Small Insects in Museums Using Illumina Sequencing

机译:使用Illumina测序成功从博物馆中的小昆虫中成功恢复核蛋白编码基因

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摘要

In this paper we explore high-throughput Illumina sequencing of nuclear protein-coding, ribosomal, and mitochondrial genes in small, dried insects stored in natural history collections. We sequenced one tenebrionid beetle and 12 carabid beetles ranging in size from 3.7 to 9.7 mm in length that have been stored in various museums for 4 to 84 years. Although we chose a number of old, small specimens for which we expected low sequence recovery, we successfully recovered at least some low-copy nuclear protein-coding genes from all specimens. For example, in one 56-year-old beetle, 4.4 mm in length, our de novo assembly recovered about 63% of approximately 41,900 nucleotides in a target suite of 67 nuclear protein-coding gene fragments, and 70% using a reference-based assembly. Even in the least successfully sequenced carabid specimen, reference-based assembly yielded fragments that were at least 50% of the target length for 34 of 67 nuclear protein-coding gene fragments. Exploration of alternative references for reference-based assembly revealed few signs of bias created by the reference. For all specimens we recovered almost complete copies of ribosomal and mitochondrial genes. We verified the general accuracy of the sequences through comparisons with sequences obtained from PCR and Sanger sequencing, including of conspecific, fresh specimens, and through phylogenetic analysis that tested the placement of sequences in predicted regions. A few possible inaccuracies in the sequences were detected, but these rarely affected the phylogenetic placement of the samples. Although our sample sizes are low, an exploratory regression study suggests that the dominant factor in predicting success at recovering nuclear protein-coding genes is a high number of Illumina reads, with success at PCR of COI and killing by immersion in ethanol being secondary factors; in analyses of only high-read samples, the primary significant explanatory variable was body length, with small beetles being more successfully sequenced.
机译:在本文中,我们探索了自然历史资料集中存储的小型干燥昆虫中核蛋白编码,核糖体和线粒体基因的高通量Illumina测序。我们对一只变种甲虫和12个甲壳虫进行了测序,这些甲虫的大小从3.7毫米到9.7毫米不等,已经在各种博物馆中保存了4到84年。尽管我们选择了一些预期可低序列回收的旧小样本,但我们已成功从所有样本中成功回收了至少一些低拷贝核蛋白编码基因。例如,在一头56岁的甲壳虫(长4.4毫米)中,我们的从头装配体从67个核蛋白编码基因片段的靶标集中回收了约41,900个核苷酸的63%,而使用基于参考的部件。即使是在测序最不成功的Carabid标本中,基于参考的装配所产生的片段也至少是67个核蛋白编码基因片段中34个的目标长度的50%。对基于参考的程序集的替代参考的探索表明,该参考几乎没有产生偏差的迹象。对于所有标本,我们回收了几乎完整的核糖体和线粒体基因拷贝。我们通过与从PCR和Sanger测序获得的序列(包括同种的新鲜标本)进行比较,并通过系统发育分析测试了序列在预测区域中的位置,从而验证了序列的总体准确性。检测到序列中可能存在的一些误差,但是这些误差很少影响样本的系统发育位置。尽管我们的样本量很小,但一项探索性回归研究表明,预测成功恢复核蛋白编码基因成功的主要因素是大量的Illumina读物,其中成功进行COI PCR和浸入乙醇杀死是次要因素。在仅对高读样本进行分析时,主要的解释性变量是体长,小甲虫的测序更为成功。

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