Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/138438
Title: A pan-cetacean MHC amplicon sequencing panel developed and evaluated in combination with genome assemblies
Authors: Heimeier, Dorothea
Garland, Ellen C.
Eichenberger, Franca
Garrigue, Claire
Vella, Adriana
Baker, C. Scott
Carroll, Emma L.
Keywords: Cetacea -- Mediterranean Sea
Introduced organisms -- Mediterranean Sea
Marine biodiversity conservation -- Law and legislation
Sustainable development -- Mediterranean Region
Humpback whale -- Mediterranean Sea
Major histocompatibility complex
Histocompatibility
Southern right whale -- Mediterranean Sea
Issue Date: 2024
Publisher: John Wiley & Sons Ltd.
Citation: Heimeier, D., Garland, E. C., Eichenberger, F., Garrigue, C., Vella, A., Baker, C. S., & Carroll, E. L. (2024). A pan‐cetacean MHC amplicon sequencing panel developed and evaluated in combination with genome assemblies. Molecular Ecology Resources, 24(5), e13955.
Abstract: The major histocompatibility complex (MHC) is a highly polymorphic gene family that is crucial in immunity, and its diversity can be effectively used as a fitness marker for populations. Despite this, MHC remains poorly characterised in non-model species (e.g., cetaceans: whales, dolphins and porpoises) as high gene copy number variation, especially in the fast-evolving class I region, makes analyses of genomic sequences difficult. To date, only small sections of class I and IIa genes have been used to assess functional diversity in cetacean populations. Here, we undertook a systematic characterisation of the MHC class I and IIa regions in available cetacean genomes. We extracted full-length gene sequences to design pan-cetacean primers that amplified the complete exon 2 from MHC class I and IIa genes in one combined sequencing panel. We validated this panel in 19 cetacean species and described 354 alleles for both classes. Furthermore, we identified likely assembly artefacts for many MHC class I assemblies based on the presence of class I genes in the amplicon data compared to missing genes from genomes. Finally, we investigated MHC diversity using the panel in 25 humpback and 30 southern right whales, including four paternity trios for humpback whales. This revealed copy-number variable class I haplotypes in humpback whales, which is likely a common phenomenon across cetaceans. These MHC alleles will form the basis for a cetacean branch of the Immuno-Polymorphism Database (IPD-MHC), a curated resource intended to aid in the systematic compilation of MHC alleles across several species, to support conservation initiatives.
URI: https://www.um.edu.mt/library/oar/handle/123456789/138438
Appears in Collections:Scholarly Works - FacSciBio



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