Genomics of cold adaptations in the Antarctic notothenioid fish radiation

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作者
Iliana Bista
Jonathan M. D. Wood
Thomas Desvignes
Shane A. McCarthy
Michael Matschiner
Zemin Ning
Alan Tracey
James Torrance
Ying Sims
William Chow
Michelle Smith
Karen Oliver
Leanne Haggerty
Walter Salzburger
John H. Postlethwait
Kerstin Howe
Melody S. Clark
H. William Detrich
C.-H. Christina Cheng
Eric A. Miska
Richard Durbin
机构
[1] Wellcome Genome Campus,Wellcome Sanger Institute, Tree of Life
[2] University of Cambridge,Department of Genetics
[3] University of Cambridge,Wellcome/CRUK Gurdon Institute
[4] Naturalis Biodiversity Center,European Molecular Biology Laboratory, European Bioinformatics Institute
[5] University of Oregon,Department of Evolution, Ecology, and Behaviour
[6] Institute of Neuroscience,undefined
[7] 1254 University of Oregon,undefined
[8] University of Oslo,undefined
[9] Natural History Museum,undefined
[10] University of Oslo,undefined
[11] University of Zurich,undefined
[12] Department of Palaeontology and Museum,undefined
[13] University of Zurich,undefined
[14] Wellcome Genome Campus,undefined
[15] University of Basel,undefined
[16] Zoological Institute,undefined
[17] Department of Environmental Sciences,undefined
[18] British Antarctic Survey,undefined
[19] High Cross,undefined
[20] Northeastern University,undefined
[21] Department of Marine and Environmental Sciences,undefined
[22] Marine Science Centre,undefined
[23] University of Illinois,undefined
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摘要
Numerous novel adaptations characterise the radiation of notothenioids, the dominant fish group in the freezing seas of the Southern Ocean. To improve understanding of the evolution of this iconic fish group, here we generate and analyse new genome assemblies for 24 species covering all major subgroups of the radiation, including five long-read assemblies. We present a new estimate for the onset of the radiation at 10.7 million years ago, based on a time-calibrated phylogeny derived from genome-wide sequence data. We identify a two-fold variation in genome size, driven by expansion of multiple transposable element families, and use the long-read data to reconstruct two evolutionarily important, highly repetitive gene family loci. First, we present the most complete reconstruction to date of the antifreeze glycoprotein gene family, whose emergence enabled survival in sub-zero temperatures, showing the expansion of the antifreeze gene locus from the ancestral to the derived state. Second, we trace the loss of haemoglobin genes in icefishes, the only vertebrates lacking functional haemoglobins, through complete reconstruction of the two haemoglobin gene clusters across notothenioid families. Both the haemoglobin and antifreeze genomic loci are characterised by multiple transposon expansions that may have driven the evolutionary history of these genes.
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