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Genome and transcriptome mechanisms driving cephalopod evolution
Cephalopods are known for their large nervous systems, complex behaviors and morphological innovations. To investigate the genomic underpinnings of these features, we assembled the chromosomes of the Boston market squid, Doryteuthis (Loligo) pealeii, and the California two-spot octopus, Octopus bima...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068888/ https://www.ncbi.nlm.nih.gov/pubmed/35508532 http://dx.doi.org/10.1038/s41467-022-29748-w |
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author | Albertin, Caroline B. Medina-Ruiz, Sofia Mitros, Therese Schmidbaur, Hannah Sanchez, Gustavo Wang, Z. Yan Grimwood, Jane Rosenthal, Joshua J. C. Ragsdale, Clifton W. Simakov, Oleg Rokhsar, Daniel S. |
author_facet | Albertin, Caroline B. Medina-Ruiz, Sofia Mitros, Therese Schmidbaur, Hannah Sanchez, Gustavo Wang, Z. Yan Grimwood, Jane Rosenthal, Joshua J. C. Ragsdale, Clifton W. Simakov, Oleg Rokhsar, Daniel S. |
author_sort | Albertin, Caroline B. |
collection | PubMed |
description | Cephalopods are known for their large nervous systems, complex behaviors and morphological innovations. To investigate the genomic underpinnings of these features, we assembled the chromosomes of the Boston market squid, Doryteuthis (Loligo) pealeii, and the California two-spot octopus, Octopus bimaculoides, and compared them with those of the Hawaiian bobtail squid, Euprymna scolopes. The genomes of the soft-bodied (coleoid) cephalopods are highly rearranged relative to other extant molluscs, indicating an intense, early burst of genome restructuring. The coleoid genomes feature multi-megabase, tandem arrays of genes associated with brain development and cephalopod-specific innovations. We find that a known coleoid hallmark, extensive A-to-I mRNA editing, displays two fundamentally distinct patterns: one exclusive to the nervous system and concentrated in genic sequences, the other widespread and directed toward repetitive elements. We conclude that coleoid novelty is mediated in part by substantial genome reorganization, gene family expansion, and tissue-dependent mRNA editing. |
format | Online Article Text |
id | pubmed-9068888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90688882022-05-05 Genome and transcriptome mechanisms driving cephalopod evolution Albertin, Caroline B. Medina-Ruiz, Sofia Mitros, Therese Schmidbaur, Hannah Sanchez, Gustavo Wang, Z. Yan Grimwood, Jane Rosenthal, Joshua J. C. Ragsdale, Clifton W. Simakov, Oleg Rokhsar, Daniel S. Nat Commun Article Cephalopods are known for their large nervous systems, complex behaviors and morphological innovations. To investigate the genomic underpinnings of these features, we assembled the chromosomes of the Boston market squid, Doryteuthis (Loligo) pealeii, and the California two-spot octopus, Octopus bimaculoides, and compared them with those of the Hawaiian bobtail squid, Euprymna scolopes. The genomes of the soft-bodied (coleoid) cephalopods are highly rearranged relative to other extant molluscs, indicating an intense, early burst of genome restructuring. The coleoid genomes feature multi-megabase, tandem arrays of genes associated with brain development and cephalopod-specific innovations. We find that a known coleoid hallmark, extensive A-to-I mRNA editing, displays two fundamentally distinct patterns: one exclusive to the nervous system and concentrated in genic sequences, the other widespread and directed toward repetitive elements. We conclude that coleoid novelty is mediated in part by substantial genome reorganization, gene family expansion, and tissue-dependent mRNA editing. Nature Publishing Group UK 2022-05-04 /pmc/articles/PMC9068888/ /pubmed/35508532 http://dx.doi.org/10.1038/s41467-022-29748-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Albertin, Caroline B. Medina-Ruiz, Sofia Mitros, Therese Schmidbaur, Hannah Sanchez, Gustavo Wang, Z. Yan Grimwood, Jane Rosenthal, Joshua J. C. Ragsdale, Clifton W. Simakov, Oleg Rokhsar, Daniel S. Genome and transcriptome mechanisms driving cephalopod evolution |
title | Genome and transcriptome mechanisms driving cephalopod evolution |
title_full | Genome and transcriptome mechanisms driving cephalopod evolution |
title_fullStr | Genome and transcriptome mechanisms driving cephalopod evolution |
title_full_unstemmed | Genome and transcriptome mechanisms driving cephalopod evolution |
title_short | Genome and transcriptome mechanisms driving cephalopod evolution |
title_sort | genome and transcriptome mechanisms driving cephalopod evolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068888/ https://www.ncbi.nlm.nih.gov/pubmed/35508532 http://dx.doi.org/10.1038/s41467-022-29748-w |
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