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Does One Size Fit All? Variations in the DNA Barcode Gaps of Macrofungal Genera
Andrew W Wilson1, Ursula Eberhardt2, Nhu Nguyen3
1Denver Botanic Gardens, 909 York Street, Denver, CO 80206, USA.
Understanding the DNA barcode gap in macrofungi is crucial for fungal diversity studies. This research reveals variations in the nuclear ribosomal internal transcribed spacer (nrITS) region, impacting species identification accuracy.
Area of Science:
- Mycology
- Molecular Biology
- Genetics
Background:
- The nuclear ribosomal internal transcribed spacer (nrITS) region is a key DNA barcode for fungal diversity and distribution studies.
- Environmental metabarcoding highlights the need for robust fungal DNA barcoding practices.
- Limited understanding of the DNA barcode gap in macrofungi hinders accurate species delineation.
Purpose of the Study:
- To examine the DNA barcode gap within the nrITS region of macrofungi.
- To investigate factors influencing barcode gap size, including sequence variance and taxonomic approaches.
- To assess the implications for quantifying fungal species richness and taxonomic studies.
Main Methods:
- Analysis of 5146 nrITS sequences from 717 macrofungi species.
- Measurement of intra- and inter-specific pairwise distances using sequence and phylogenetic data.
- Comparison of barcode gap variations between ITS1, ITS2, and combined nrITS regions.
Main Results:
- Barcode gap size is influenced by intra- and inter-specific variance.
- The ITS2 region exhibits greater barcode gaps than ITS1 due to higher variance.
- Taxonomic 'splitting' yields larger barcode gaps compared to 'lumping'.
Conclusions:
- Variability in nrITS barcode gaps necessitates careful consideration for species richness estimation.
- Understanding barcode gap behavior is essential for accurate fungal DNA barcoding.
- Multiple molecular markers are recommended to corroborate species delineation in taxonomic studies.
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