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蛋白质编码低拷贝区域是可行的真菌代谢条形码DNA标记,可补充ITS以提高准确性。

Protein Coding Low-Copy and Regions Are Viable Fungal Metabarcoding DNA Markers Which Can Supplement ITS for Better Accuracy.

作者信息

Shapkin Vasilii, Caboň Miroslav, Kolařík Miroslav, Adamčíková Katarína, Baldrian Petr, Michalková Tereza, Větrovský Tomáš, Adamčík Slavomír

机构信息

Laboratory of Molecular Ecology and Mycology Institute of Botany, Plant Science and Biodiversity Center, Slovak Academy of Sciences Bratislava Slovakia.

Department of Plant Pathology University of Florida Gainesville Florida USA.

出版信息

Ecol Evol. 2025 Apr 21;15(4):e71352. doi: 10.1002/ece3.71352. eCollection 2025 Apr.

Abstract

The nuclear ribosomal DNA Internal Transcribed Spacer (ITS) region is used as a universal fungal barcode marker, but often lacks a significant DNA barcoding gap between sister taxa. Here we tested the reliability of protein coding low-copy genes as alternative barcode markers. Mock communities of three unrelated agaric genera (, , and ) representing lineages of closely related species were sequenced by the Illumina platform targeting the ITS1, ITS2, the second largest subunit of RNA polymerase II gene () and the transcription elongation factor 1-alpha gene () regions. Species representation and their relative abundances were similar across all tested barcode regions, despite a lower copy number in protein coding markers. ITS1 and ITS2 required more sophisticated sequence filtering because they produced a high number of chimeric sequences requiring reference-based chimera removal and had a higher number of sequence variants per species. Although clustering of filtered ITS sequences resulted in an average higher number of correctly clustered units at optimal similarity thresholds, these thresholds varied substantially among genera. Best-fitted thresholds of low-copy markers were more consistent across genera but frequently lacked species resolution due to low intraspecific variability. At some thresholds, we observed multiple species lumped together, and at the same time, species split into multiple partial clusters, which should be taken into consideration when assessing the best clustering thresholds and taxonomic identity of clusters. To achieve the best taxonomic resolution and improve species detection, we recommend combining different markers and applying additional reference-based sorting of clusters. The current availability of and reference sequences in public databases is far from being complete for all fungal groups, but a combined marker approach can be used for group-specific studies that can build reference data for their own purposes.

摘要

核糖体DNA内转录间隔区(ITS)被用作通用的真菌条形码标记,但姐妹分类群之间往往缺乏显著的DNA条形码间隙。在此,我们测试了蛋白质编码低拷贝基因作为替代条形码标记的可靠性。利用Illumina平台对代表近缘物种谱系的三个无关伞菌属(、和)的模拟群落进行测序,目标区域为ITS1、ITS2、RNA聚合酶II基因的第二大亚基()和转录延伸因子1-α基因()区域。尽管蛋白质编码标记中的拷贝数较低,但在所有测试的条形码区域中,物种代表性及其相对丰度相似。ITS1和ITS2需要更复杂的序列过滤,因为它们产生了大量嵌合序列,需要基于参考的嵌合体去除,并且每个物种的序列变异数量更多。尽管在最佳相似性阈值下,过滤后的ITS序列聚类导致平均有更多正确聚类的单元,但这些阈值在不同属之间差异很大。低拷贝标记的最佳拟合阈值在不同属之间更一致,但由于种内变异性低,常常缺乏物种分辨率。在某些阈值下,我们观察到多个物种被归为一类,同时,物种又被分成多个部分聚类,在评估最佳聚类阈值和聚类的分类身份时应考虑到这一点。为了实现最佳的分类分辨率并提高物种检测,我们建议结合不同的标记,并对聚类应用额外的基于参考的分类。公共数据库中目前的和参考序列对于所有真菌类群来说远未完整,但联合标记方法可用于特定类群的研究,这些研究可以为自身目的构建参考数据。

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