Six new reference-quality bat genomes illuminate the molecular basis and evolution of bat adaptations
David JebbiD, Zixia HuangiD, Martin PippeliD, Graham M. HughesiD, Ksenia Lavrichenko, Paolo DevannaiD, Sylke WinkleriD, Lars Sommer JermiiniD, Emilia C. SkirmunttiD, Aris KatzourakisiD, Lucy Burkitt-GrayiD, David A. RayiD, Kevin A. M. SullivaniD, Juliana G. RoscitoiD, Bogdan KirilenkoiD, Liliana M. DávalosiD, Angélique CorthalsiD, Megan L. PoweriD, Gareth JonesiD, Roger D. RansomeiD, Dina K. N. DechmanniD, Andrea G. LocatelliiD, Sébastien J. PuechmailleiD, Olivier D. FedrigoiD, Erich David JarvisiD, , Emma C. TeelingiD
Abstract
Bats account for ~20% of all extant mammal species and are considered exceptional given their extraordinary adaptations, including biosonar, true flight, extreme longevity, and unparalleled immune systems. To understand these adaptations, we generated reference-quality genomes of six species representing the key divergent lineages. We assembled these genomes with a novel pipeline incorporating state-of-the-art long-read and long-range sequencing and assembly techniques. The genomes were annotated using a maximal evidence approach, de novo predictions, protein/mRNA alignments, Iso-seq long read and RNA-seq short read transcripts, and gene projections from our new TOGA pipeline, retrieving virtually all (>99%) mammalian BUSCO genes. Phylogenetic analyses of 12,931 protein coding-genes and 10,857 conserved non-coding elements identified across 48 mammalian genomes helped to resolve bats closest extant relatives within Laurasiatheria, supporting a basal position for bats within Scrotifera. Genome-wide screens along the bat ancestral branch revealed (a) selection on hearing-involved genes (e.g LRP2, SERPINB6, TJP2), which suggest that laryngeal echolocation is a shared ancestral trait of bats; (b) selection (e.g INAVA, CXCL13, NPSR1) and loss of immunity related proteins (e.g. LRRC70, IL36G), including pro-inflammatory NF-kB signalling; and (c) expansion of the APOBEC family, associated with restricting viral infection, transposon activity and interferon signalling. We also identified unique integrated viruses, indicating that bats have a history of tolerating viral pathogens, lethal to other mammal species. Non-coding RNA analyses identified variant and novel microRNAs, revealing regulatory relationships that may contribute to phenotypic diversity in bats. Together, our reference-quality genomes, high-quality annotations, genome-wide screens and in-vitro tests revealed previously unknown genomic adaptations in bats that may explain their extraordinary traits.
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