Author
Listed:
- Yang Zhou
(BGI-Shenzhen
Department of Biology, University of Copenhagen)
- Linda Shearwin-Whyatt
(The University of Adelaide)
- Jing Li
(Zhejiang University)
- Zhenzhen Song
(BGI-Shenzhen
University of Chinese Academy of Sciences)
- Takashi Hayakawa
(Hokkaido University
Japan Monkey Centre)
- David Stevens
(The University of Adelaide)
- Jane C. Fenelon
(The University of Melbourne)
- Emma Peel
(The University of Sydney)
- Yuanyuan Cheng
(The University of Sydney)
- Filip Pajpach
(The University of Adelaide)
- Natasha Bradley
(The University of Adelaide)
- Hikoyu Suzuki
(digzyme Inc)
- Masato Nikaido
(School of Life Science and Technology, Tokyo Institute of Technology)
- Joana Damas
(University of California)
- Tasman Daish
(The University of Adelaide)
- Tahlia Perry
(The University of Adelaide)
- Zexian Zhu
(Zhejiang University)
- Yuncong Geng
(Johns Hopkins University)
- Arang Rhie
(National Institutes of Health)
- Ying Sims
(Tree of Life Programme, Wellcome Sanger Institute)
- Jonathan Wood
(Tree of Life Programme, Wellcome Sanger Institute)
- Bettina Haase
(The Rockefeller University)
- Jacquelyn Mountcastle
(The Rockefeller University)
- Olivier Fedrigo
(The Rockefeller University)
- Qiye Li
(BGI-Shenzhen)
- Huanming Yang
(BGI-Shenzhen
James D. Watson Institute of Genome Sciences
University of the Chinese Academy of Sciences
BGI-Shenzhen)
- Jian Wang
(BGI-Shenzhen
James D. Watson Institute of Genome Sciences)
- Stephen D. Johnston
(The University of Queensland)
- Adam M. Phillippy
(National Institutes of Health)
- Kerstin Howe
(Tree of Life Programme, Wellcome Sanger Institute)
- Erich D. Jarvis
(The Rockefeller University
Howard Hughes Medical Institute)
- Oliver A. Ryder
(San Diego Zoo Global)
- Henrik Kaessmann
(Center for Molecular Biology of Heidelberg University (ZMBH), DKFZ-ZMBH Alliance)
- Peter Donnelly
(University of Oxford)
- Jonas Korlach
(Pacific Biosciences)
- Harris A. Lewin
(University of California
University of California
University of California)
- Jennifer Graves
(Australian National University
University of Canberra
La Trobe University)
- Katherine Belov
(The University of Sydney)
- Marilyn B. Renfree
(The University of Melbourne)
- Frank Grutzner
(The University of Adelaide)
- Qi Zhou
(Zhejiang University
University of Vienna
Zhejiang University)
- Guojie Zhang
(BGI-Shenzhen
Department of Biology, University of Copenhagen
Kunming Institute of Zoology, Chinese Academy of Sciences
Chinese Academy of Sciences)
Abstract
Egg-laying mammals (monotremes) are the only extant mammalian outgroup to therians (marsupial and eutherian animals) and provide key insights into mammalian evolution1,2. Here we generate and analyse reference genomes of the platypus (Ornithorhynchus anatinus) and echidna (Tachyglossus aculeatus), which represent the only two extant monotreme lineages. The nearly complete platypus genome assembly has anchored almost the entire genome onto chromosomes, markedly improving the genome continuity and gene annotation. Together with our echidna sequence, the genomes of the two species allow us to detect the ancestral and lineage-specific genomic changes that shape both monotreme and mammalian evolution. We provide evidence that the monotreme sex chromosome complex originated from an ancestral chromosome ring configuration. The formation of such a unique chromosome complex may have been facilitated by the unusually extensive interactions between the multi-X and multi-Y chromosomes that are shared by the autosomal homologues in humans. Further comparative genomic analyses unravel marked differences between monotremes and therians in haptoglobin genes, lactation genes and chemosensory receptor genes for smell and taste that underlie the ecological adaptation of monotremes.
Suggested Citation
Yang Zhou & Linda Shearwin-Whyatt & Jing Li & Zhenzhen Song & Takashi Hayakawa & David Stevens & Jane C. Fenelon & Emma Peel & Yuanyuan Cheng & Filip Pajpach & Natasha Bradley & Hikoyu Suzuki & Masato, 2021.
"Platypus and echidna genomes reveal mammalian biology and evolution,"
Nature, Nature, vol. 592(7856), pages 756-762, April.
Handle:
RePEc:nat:nature:v:592:y:2021:i:7856:d:10.1038_s41586-020-03039-0
DOI: 10.1038/s41586-020-03039-0
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Cited by:
- Milan Kumar Samanta & Srimonta Gayen & Clair Harris & Emily Maclary & Yumie Murata-Nakamura & Rebecca M. Malcore & Robert S. Porter & Patricia M. Garay & Christina N. Vallianatos & Paul B. Samollow & , 2022.
"Activation of Xist by an evolutionarily conserved function of KDM5C demethylase,"
Nature Communications, Nature, vol. 13(1), pages 1-16, December.
- Rose Wellens & Victor S. Tapia & Paula I. Seoane & Hayley Bennett & Antony Adamson & Graham Coutts & Jack Rivers-Auty & Martin Lowe & Jack P. Green & Gloria Lopez-Castejon & David Brough & Christopher, 2024.
"Proximity labelling of pro-interleukin-1α reveals evolutionary conserved nuclear interactions,"
Nature Communications, Nature, vol. 15(1), pages 1-16, December.
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