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Evaluating the performance of targeted sequence capture, RNA‐Seq, and degenerate‐primer PCR cloning for sequencing the largest mammalian multigene family
Author(s) -
Yohe Laurel R.,
Davies Kalina T. J.,
Simmons Nancy B.,
Sears Karen E.,
Dumont Elizabeth R.,
Rossiter Stephen J.,
Dávalos Liliana M.
Publication year - 2020
Publication title -
molecular ecology resources
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.96
H-Index - 136
eISSN - 1755-0998
pISSN - 1755-098X
DOI - 10.1111/1755-0998.13093
Subject(s) - biology , genetics , genome , sanger sequencing , gene , amplicon , pseudogene , reference genome , sequence assembly , computational biology , gene prediction , gene family , dna sequencing , transcriptome , polymerase chain reaction , gene expression
Multigene families evolve from single‐copy ancestral genes via duplication, and typically encode proteins critical to key biological processes. Molecular analyses of these gene families require high‐confidence sequences, but the high sequence similarity of the members can create challenges for sequencing and downstream analyses. Focusing on the common vampire bat, Desmodus rotundus , we evaluated how different sequencing approaches performed in recovering the largest mammalian protein‐coding multigene family: olfactory receptors (OR). Using the genome as a reference, we determined the proportion of intact protein‐coding receptors recovered by: (a) amplicons from degenerate primers sequenced via Sanger technology, (b) RNA‐Seq of the main olfactory epithelium, and (c) those genes captured with probes designed from transcriptomes of closely‐related species. Our initial re‐annotation of the high‐quality vampire bat genome resulted in >400 intact OR genes, more than doubling the original estimate. Sanger‐sequenced amplicons performed the poorest among the three approaches, detecting <33% of receptors in the genome. In contrast, the transcriptome reliably recovered >50% of the annotated genomic ORs, and targeted sequence capture recovered nearly 75% of annotated genes. Each sequencing approach assembled high‐quality sequences, even if it did not recover all receptors in the genome. While some variation may be due to limitations of the study design (e.g., different individuals), variation among approaches was mostly caused by low coverage of some receptors rather than high rates of assembly error. Given this variability, we caution against using the counts of intact receptors per species to model the birth‐death process of multigene families. Instead, our results support the use of orthologous sequences to explore and model the evolutionary processes shaping these genes.