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Millipede genomes reveal unique adaptations during myriapod evolution

The Myriapoda, composed of millipedes and centipedes, is a fascinating but poorly understood branch of life, including species with a highly unusual body plan and a range of unique adaptations to their environment. Here, we sequenced and assembled 2 chromosomal-level genomes of the millipedes Helico...

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Autores principales: Qu, Zhe, Nong, Wenyan, So, Wai Lok, Barton-Owen, Tom, Li, Yiqian, Leung, Thomas C. N., Li, Chade, Baril, Tobias, Wong, Annette Y. P., Swale, Thomas, Chan, Ting-Fung, Hayward, Alexander, Ngai, Sai-Ming, Hui, Jerome H. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523956/
https://www.ncbi.nlm.nih.gov/pubmed/32991578
http://dx.doi.org/10.1371/journal.pbio.3000636
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author Qu, Zhe
Nong, Wenyan
So, Wai Lok
Barton-Owen, Tom
Li, Yiqian
Leung, Thomas C. N.
Li, Chade
Baril, Tobias
Wong, Annette Y. P.
Swale, Thomas
Chan, Ting-Fung
Hayward, Alexander
Ngai, Sai-Ming
Hui, Jerome H. L.
author_facet Qu, Zhe
Nong, Wenyan
So, Wai Lok
Barton-Owen, Tom
Li, Yiqian
Leung, Thomas C. N.
Li, Chade
Baril, Tobias
Wong, Annette Y. P.
Swale, Thomas
Chan, Ting-Fung
Hayward, Alexander
Ngai, Sai-Ming
Hui, Jerome H. L.
author_sort Qu, Zhe
collection PubMed
description The Myriapoda, composed of millipedes and centipedes, is a fascinating but poorly understood branch of life, including species with a highly unusual body plan and a range of unique adaptations to their environment. Here, we sequenced and assembled 2 chromosomal-level genomes of the millipedes Helicorthomorpha holstii (assembly size = 182 Mb; shortest scaffold/contig length needed to cover 50% of the genome [N50] = 18.11 Mb mainly on 8 pseudomolecules) and Trigoniulus corallinus (assembly size = 449 Mb, N50 = 26.78 Mb mainly on 17 pseudomolecules). Unique genomic features, patterns of gene regulation, and defence systems in millipedes, not observed in other arthropods, are revealed. Both repeat content and intron size are major contributors to the observed differences in millipede genome size. Tight Hox and the first loose ecdysozoan ParaHox homeobox clusters are identified, and a myriapod-specific genomic rearrangement including Hox3 is also observed. The Argonaute (AGO) proteins for loading small RNAs are duplicated in both millipedes, but unlike in insects, an AGO duplicate has become a pseudogene. Evidence of post-transcriptional modification in small RNAs—including species-specific microRNA arm switching—providing differential gene regulation is also obtained. Millipedes possesses a unique ozadene defensive gland unlike the venomous forcipules found in centipedes. We identify sets of genes associated with the ozadene that play roles in chemical defence as well as antimicrobial activity. Macro-synteny analyses revealed highly conserved genomic blocks between the 2 millipedes and deuterostomes. Collectively, our analyses of millipede genomes reveal that a series of unique adaptations have occurred in this major lineage of arthropod diversity. The 2 high-quality millipede genomes provided here shed new light on the conserved and lineage-specific features of millipedes and centipedes. These findings demonstrate the importance of the consideration of both centipede and millipede genomes—and in particular the reconstruction of the myriapod ancestral situation—for future research to improve understanding of arthropod evolution, and animal evolutionary genomics more widely.
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spelling pubmed-75239562020-10-06 Millipede genomes reveal unique adaptations during myriapod evolution Qu, Zhe Nong, Wenyan So, Wai Lok Barton-Owen, Tom Li, Yiqian Leung, Thomas C. N. Li, Chade Baril, Tobias Wong, Annette Y. P. Swale, Thomas Chan, Ting-Fung Hayward, Alexander Ngai, Sai-Ming Hui, Jerome H. L. PLoS Biol Research Article The Myriapoda, composed of millipedes and centipedes, is a fascinating but poorly understood branch of life, including species with a highly unusual body plan and a range of unique adaptations to their environment. Here, we sequenced and assembled 2 chromosomal-level genomes of the millipedes Helicorthomorpha holstii (assembly size = 182 Mb; shortest scaffold/contig length needed to cover 50% of the genome [N50] = 18.11 Mb mainly on 8 pseudomolecules) and Trigoniulus corallinus (assembly size = 449 Mb, N50 = 26.78 Mb mainly on 17 pseudomolecules). Unique genomic features, patterns of gene regulation, and defence systems in millipedes, not observed in other arthropods, are revealed. Both repeat content and intron size are major contributors to the observed differences in millipede genome size. Tight Hox and the first loose ecdysozoan ParaHox homeobox clusters are identified, and a myriapod-specific genomic rearrangement including Hox3 is also observed. The Argonaute (AGO) proteins for loading small RNAs are duplicated in both millipedes, but unlike in insects, an AGO duplicate has become a pseudogene. Evidence of post-transcriptional modification in small RNAs—including species-specific microRNA arm switching—providing differential gene regulation is also obtained. Millipedes possesses a unique ozadene defensive gland unlike the venomous forcipules found in centipedes. We identify sets of genes associated with the ozadene that play roles in chemical defence as well as antimicrobial activity. Macro-synteny analyses revealed highly conserved genomic blocks between the 2 millipedes and deuterostomes. Collectively, our analyses of millipede genomes reveal that a series of unique adaptations have occurred in this major lineage of arthropod diversity. The 2 high-quality millipede genomes provided here shed new light on the conserved and lineage-specific features of millipedes and centipedes. These findings demonstrate the importance of the consideration of both centipede and millipede genomes—and in particular the reconstruction of the myriapod ancestral situation—for future research to improve understanding of arthropod evolution, and animal evolutionary genomics more widely. Public Library of Science 2020-09-29 /pmc/articles/PMC7523956/ /pubmed/32991578 http://dx.doi.org/10.1371/journal.pbio.3000636 Text en © 2020 Qu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Qu, Zhe
Nong, Wenyan
So, Wai Lok
Barton-Owen, Tom
Li, Yiqian
Leung, Thomas C. N.
Li, Chade
Baril, Tobias
Wong, Annette Y. P.
Swale, Thomas
Chan, Ting-Fung
Hayward, Alexander
Ngai, Sai-Ming
Hui, Jerome H. L.
Millipede genomes reveal unique adaptations during myriapod evolution
title Millipede genomes reveal unique adaptations during myriapod evolution
title_full Millipede genomes reveal unique adaptations during myriapod evolution
title_fullStr Millipede genomes reveal unique adaptations during myriapod evolution
title_full_unstemmed Millipede genomes reveal unique adaptations during myriapod evolution
title_short Millipede genomes reveal unique adaptations during myriapod evolution
title_sort millipede genomes reveal unique adaptations during myriapod evolution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523956/
https://www.ncbi.nlm.nih.gov/pubmed/32991578
http://dx.doi.org/10.1371/journal.pbio.3000636
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