Topological structures and syntenic conservation in sea anemone genomes
Abstract There is currently little information about the evolution of gene clusters, genome architectures and karyotypes in early branching animals. Slowly evolving anthozoan cnidarians can be particularly informative about the evolution of these genome features. Here we report chromosome-level geno...
| Published in: | Nature Communications |
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Nature Portfolio
2023-12-01
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| Online Access: | https://doi.org/10.1038/s41467-023-44080-7 |
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| author | Bob Zimmermann Juan D. Montenegro Sofia M. C. Robb Whitney J. Fropf Lukas Weilguny Shuonan He Shiyuan Chen Jessica Lovegrove-Walsh Eric M. Hill Cheng-Yi Chen Katerina Ragkousi Daniela Praher David Fredman Darrin Schultz Yehu Moran Oleg Simakov Grigory Genikhovich Matthew C. Gibson Ulrich Technau |
| author_facet | Bob Zimmermann Juan D. Montenegro Sofia M. C. Robb Whitney J. Fropf Lukas Weilguny Shuonan He Shiyuan Chen Jessica Lovegrove-Walsh Eric M. Hill Cheng-Yi Chen Katerina Ragkousi Daniela Praher David Fredman Darrin Schultz Yehu Moran Oleg Simakov Grigory Genikhovich Matthew C. Gibson Ulrich Technau |
| author_sort | Bob Zimmermann |
| collection | DOAJ |
| container_title | Nature Communications |
| description | Abstract There is currently little information about the evolution of gene clusters, genome architectures and karyotypes in early branching animals. Slowly evolving anthozoan cnidarians can be particularly informative about the evolution of these genome features. Here we report chromosome-level genome assemblies of two related anthozoans, the sea anemones Nematostella vectensis and Scolanthus callimorphus. We find a robust set of 15 chromosomes with a clear one-to-one correspondence between the two species. Both genomes show chromosomal conservation, allowing us to reconstruct ancestral cnidarian and metazoan chromosomal blocks, consisting of at least 19 and 16 ancestral linkage groups, respectively. We show that, in contrast to Bilateria, the Hox and NK clusters of investigated cnidarians are largely disintegrated, despite the presence of staggered hox/gbx expression in Nematostella. This loss of microsynteny conservation may be facilitated by shorter distances between cis-regulatory sequences and their cognate transcriptional start sites. We find no clear evidence for topologically associated domains, suggesting fundamental differences in long-range gene regulation compared to vertebrates. These data suggest that large sets of ancestral metazoan genes have been retained in ancestral linkage groups of some extant lineages; yet, higher order gene regulation with associated 3D architecture may have evolved only after the cnidarian-bilaterian split. |
| format | Article |
| id | doaj-art-e35a3e97d0bc4c1fa4fd5f83a916b609 |
| institution | Directory of Open Access Journals |
| issn | 2041-1723 |
| language | English |
| publishDate | 2023-12-01 |
| publisher | Nature Portfolio |
| record_format | Article |
| spelling | doaj-art-e35a3e97d0bc4c1fa4fd5f83a916b6092025-08-19T23:56:10ZengNature PortfolioNature Communications2041-17232023-12-0114111610.1038/s41467-023-44080-7Topological structures and syntenic conservation in sea anemone genomesBob Zimmermann0Juan D. Montenegro1Sofia M. C. Robb2Whitney J. Fropf3Lukas Weilguny4Shuonan He5Shiyuan Chen6Jessica Lovegrove-Walsh7Eric M. Hill8Cheng-Yi Chen9Katerina Ragkousi10Daniela Praher11David Fredman12Darrin Schultz13Yehu Moran14Oleg Simakov15Grigory Genikhovich16Matthew C. Gibson17Ulrich Technau18Department of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaStowers Institute for Medical ResearchStowers Institute for Medical ResearchDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaStowers Institute for Medical ResearchStowers Institute for Medical ResearchDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaStowers Institute for Medical ResearchStowers Institute for Medical ResearchStowers Institute for Medical ResearchDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaStowers Institute for Medical ResearchDepartment of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of ViennaAbstract There is currently little information about the evolution of gene clusters, genome architectures and karyotypes in early branching animals. Slowly evolving anthozoan cnidarians can be particularly informative about the evolution of these genome features. Here we report chromosome-level genome assemblies of two related anthozoans, the sea anemones Nematostella vectensis and Scolanthus callimorphus. We find a robust set of 15 chromosomes with a clear one-to-one correspondence between the two species. Both genomes show chromosomal conservation, allowing us to reconstruct ancestral cnidarian and metazoan chromosomal blocks, consisting of at least 19 and 16 ancestral linkage groups, respectively. We show that, in contrast to Bilateria, the Hox and NK clusters of investigated cnidarians are largely disintegrated, despite the presence of staggered hox/gbx expression in Nematostella. This loss of microsynteny conservation may be facilitated by shorter distances between cis-regulatory sequences and their cognate transcriptional start sites. We find no clear evidence for topologically associated domains, suggesting fundamental differences in long-range gene regulation compared to vertebrates. These data suggest that large sets of ancestral metazoan genes have been retained in ancestral linkage groups of some extant lineages; yet, higher order gene regulation with associated 3D architecture may have evolved only after the cnidarian-bilaterian split.https://doi.org/10.1038/s41467-023-44080-7 |
| spellingShingle | Bob Zimmermann Juan D. Montenegro Sofia M. C. Robb Whitney J. Fropf Lukas Weilguny Shuonan He Shiyuan Chen Jessica Lovegrove-Walsh Eric M. Hill Cheng-Yi Chen Katerina Ragkousi Daniela Praher David Fredman Darrin Schultz Yehu Moran Oleg Simakov Grigory Genikhovich Matthew C. Gibson Ulrich Technau Topological structures and syntenic conservation in sea anemone genomes |
| title | Topological structures and syntenic conservation in sea anemone genomes |
| title_full | Topological structures and syntenic conservation in sea anemone genomes |
| title_fullStr | Topological structures and syntenic conservation in sea anemone genomes |
| title_full_unstemmed | Topological structures and syntenic conservation in sea anemone genomes |
| title_short | Topological structures and syntenic conservation in sea anemone genomes |
| title_sort | topological structures and syntenic conservation in sea anemone genomes |
| url | https://doi.org/10.1038/s41467-023-44080-7 |
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