A nuclear genome assembly of an extinct flightless bird, the little bush moa

Author:

Edwards Scott V.12ORCID,Cloutier Alison1ORCID,Cockburn Glenn3ORCID,Driver Robert4ORCID,Grayson Phil12ORCID,Katoh Kazutaka5,Baldwin Maude W.3ORCID,Sackton Timothy B.6ORCID,Baker Allan J.78

Affiliation:

1. Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA.

2. Museum of Comparative Zoology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA.

3. Evolution of Sensory Systems Research Group, Max Planck Institute for Biological Intelligence, 82319 Seewiesen, Germany.

4. Department of Biology, East Carolina University, E 5th Street, Greenville, NC 27605, USA.

5. Department of Genome Informatics, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita 565-0871, Japan.

6. Informatics Group, Harvard University, 38 Oxford Street, Cambridge, MA 02138, USA.

7. Department of Ecology and Evolutionary Biology, University of Toronto, 25 Willcox Street, Toronto, ON M5S 3B2, Canada.

8. Department of Natural History, Royal Ontario Museum, 100 Queen’s Park, Toronto, ON M5S 2C6, Canada.

Abstract

We present a draft genome of the little bush moa ( Anomalopteryx didiformis )—one of approximately nine species of extinct flightless birds from Aotearoa, New Zealand—using ancient DNA recovered from a fossil bone from the South Island. We recover a complete mitochondrial genome at 249.9× depth of coverage and almost 900 megabases of a male moa nuclear genome at ~4 to 5× coverage, with sequence contiguity sufficient to identify more than 85% of avian universal single-copy orthologs. We describe a diverse landscape of transposable elements and satellite repeats, estimate a long-term effective population size of ~240,000, identify a diverse suite of olfactory receptor genes and an opsin repertoire with sensitivity in the ultraviolet range, show that the wingless moa phenotype is likely not attributable to gene loss or pseudogenization, and identify potential function-altering coding sequence variants in moa that could be synthesized for future functional assays. This genomic resource should support further studies of avian evolution and morphological divergence.

Publisher

American Association for the Advancement of Science (AAAS)

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