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Six new reference-quality bat genomes illuminate the molecular basis and evolution of bat adaptations

Authors :
Paolo Devanna
Sylke Winkler
Bogdan M. Kirilenko
David Jebb
Martin Pippel
Andrea G. Locatelli
Aris Katzourakis
Graham M. Hughes
Ksenia Lavrichenko
Dina Dechmann
Gareth Jones
Mark S. Springer
Michael Hiller
Kevin A.M. Sullivan
Eugene W. Myers
Roger D. Ransome
Angelique Corthals
Zixia Huang
Sonja C. Vernes
Lucy Burkitt-Gray
Erich D. Jarvis
David A. Ray
Emma C. Teeling
Emilia C. Skirmuntt
Olivier Fedrigo
Megan L. Power
Lars S. Jermiin
Sébastien J. Puechmaille
Liliana M. Dávalos
Juliana G. Roscito
Source :
BioRxiv
Publication Year :
2019
Publisher :
Cold Spring Harbor Laboratory, 2019.

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.

Details

Database :
OpenAIRE
Journal :
BioRxiv
Accession number :
edsair.doi.dedup.....ac2a188cf5b90e0a37415610fbe064c7
Full Text :
https://doi.org/10.1101/836874