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Six reference-quality genomes reveal evolution of bat adaptations

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Jebb,  David
Max Planck Institute for the Physics of Complex Systems, Max Planck Society;

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Roscito,  Juliana G.
Max Planck Institute for the Physics of Complex Systems, Max Planck Society;

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Kirilenko,  Bogdan
Max Planck Institute for the Physics of Complex Systems, Max Planck Society;

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Citation

Jebb, D., Huang, Z., Pippel, M., Hughes, G. M., Lavrichenko, K., Devanna, P., et al. (2020). Six reference-quality genomes reveal evolution of bat adaptations. Nature, 583(7817), 578-+. doi:10.1038/s41586-020-2486-3.


Cite as: http://hdl.handle.net/21.11116/0000-0007-71C3-D
Abstract
Bats possess extraordinary adaptations, including flight, echolocation, extreme longevity and unique immunity. High-quality genomes are crucial for understanding the molecular basis and evolution of these traits. Here we incorporated long-read sequencing and state-of-the-art scaffolding protocols(1)to generate, to our knowledge, the first reference-quality genomes of six bat species (Rhinolophus ferrumequinum,Rousettus aegyptiacus,Phyllostomus discolor,Myotis myotis,Pipistrellus kuhliiandMolossus molossus). We integrated gene projections from our 'Tool to infer Orthologs from Genome Alignments' (TOGA) software with de novo and homology gene predictions as well as short- and long-read transcriptomics to generate highly complete gene annotations. To resolve the phylogenetic position of bats within Laurasiatheria, we applied several phylogenetic methods to comprehensive sets of orthologous protein-coding and noncoding regions of the genome, and identified a basal origin for bats within Scrotifera. Our genome-wide screens revealed positive selection on hearing-related genes in the ancestral branch of bats, which is indicative of laryngeal echolocation being an ancestral trait in this clade. We found selection and loss of immunity-related genes (including pro-inflammatory NF-kappa B regulators) and expansions of anti-viral APOBEC3 genes, which highlights molecular mechanisms that may contribute to the exceptional immunity of bats. Genomic integrations of diverse viruses provide a genomic record of historical tolerance to viral infection in bats. Finally, we found and experimentally validated bat-specific variation in microRNAs, which may regulate bat-specific gene-expression programs. Our reference-quality bat genomes provide the resources required to uncover and validate the genomic basis of adaptations of bats, and stimulate new avenues of research that are directly relevant to human health and disease(1). Reference-quality genomes for six bat species shed light on the phylogenetic position of Chiroptera, and provide insight into the genetic underpinnings of the unique adaptations of this clade.