Cargando…
Chromosome-level genome assembly for the angiosperm Silene conica
The angiosperm genus Silene has been the subject of extensive study in the field of ecology and evolution, but the availability of high-quality reference genome sequences has been limited for this group. Here, we report a chromosome-level assembly for the genome of Silene conica based on PacBio HiFi...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508779/ https://www.ncbi.nlm.nih.gov/pubmed/37732249 http://dx.doi.org/10.1101/2023.09.05.556365 |
_version_ | 1785107608082841600 |
---|---|
author | Fields, Peter D. Weber, Melody M. Waneka, Gus Broz, Amanda K. Sloan, Daniel B. |
author_facet | Fields, Peter D. Weber, Melody M. Waneka, Gus Broz, Amanda K. Sloan, Daniel B. |
author_sort | Fields, Peter D. |
collection | PubMed |
description | The angiosperm genus Silene has been the subject of extensive study in the field of ecology and evolution, but the availability of high-quality reference genome sequences has been limited for this group. Here, we report a chromosome-level assembly for the genome of Silene conica based on PacBio HiFi, Hi-C and Bionano technologies. The assembly produced 10 scaffolds (one per chromosome) with a total length of 862 Mb and only ~1% gap content. These results confirm previous observations that S. conica and its relatives have a reduced base chromosome number relative to the genus’s ancestral state of 12. Silene conica has an exceptionally large mitochondrial genome (>11 Mb), predominantly consisting of sequence of unknown origins. Analysis of shared sequence content suggests that it is unlikely that transfer of nuclear DNA is the primary driver of this mitochondrial genome expansion. More generally, this assembly should provide a valuable resource for future genomic studies in Silene, including comparative analyses with related species that recently evolved sex chromosomes. SIGNIFICANCE: Whole-genome sequences have been largely lacking for species in the genus Silene even though these flowering plants have been used for studying ecology, evolution, and genetics for over a century. Here, we address this gap by providing a high-quality nuclear genome assembly for S. conica, a species known to have greatly accelerated rates of sequence and structural divergence in its mitochondrial and plastid genomes. This resource will be valuable in understanding the coevolutionary interactions between nuclear and cytoplasmic genomes and in comparative analyses across this highly diverse genus. |
format | Online Article Text |
id | pubmed-10508779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105087792023-09-20 Chromosome-level genome assembly for the angiosperm Silene conica Fields, Peter D. Weber, Melody M. Waneka, Gus Broz, Amanda K. Sloan, Daniel B. bioRxiv Article The angiosperm genus Silene has been the subject of extensive study in the field of ecology and evolution, but the availability of high-quality reference genome sequences has been limited for this group. Here, we report a chromosome-level assembly for the genome of Silene conica based on PacBio HiFi, Hi-C and Bionano technologies. The assembly produced 10 scaffolds (one per chromosome) with a total length of 862 Mb and only ~1% gap content. These results confirm previous observations that S. conica and its relatives have a reduced base chromosome number relative to the genus’s ancestral state of 12. Silene conica has an exceptionally large mitochondrial genome (>11 Mb), predominantly consisting of sequence of unknown origins. Analysis of shared sequence content suggests that it is unlikely that transfer of nuclear DNA is the primary driver of this mitochondrial genome expansion. More generally, this assembly should provide a valuable resource for future genomic studies in Silene, including comparative analyses with related species that recently evolved sex chromosomes. SIGNIFICANCE: Whole-genome sequences have been largely lacking for species in the genus Silene even though these flowering plants have been used for studying ecology, evolution, and genetics for over a century. Here, we address this gap by providing a high-quality nuclear genome assembly for S. conica, a species known to have greatly accelerated rates of sequence and structural divergence in its mitochondrial and plastid genomes. This resource will be valuable in understanding the coevolutionary interactions between nuclear and cytoplasmic genomes and in comparative analyses across this highly diverse genus. Cold Spring Harbor Laboratory 2023-09-07 /pmc/articles/PMC10508779/ /pubmed/37732249 http://dx.doi.org/10.1101/2023.09.05.556365 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Fields, Peter D. Weber, Melody M. Waneka, Gus Broz, Amanda K. Sloan, Daniel B. Chromosome-level genome assembly for the angiosperm Silene conica |
title | Chromosome-level genome assembly for the angiosperm Silene conica |
title_full | Chromosome-level genome assembly for the angiosperm Silene conica |
title_fullStr | Chromosome-level genome assembly for the angiosperm Silene conica |
title_full_unstemmed | Chromosome-level genome assembly for the angiosperm Silene conica |
title_short | Chromosome-level genome assembly for the angiosperm Silene conica |
title_sort | chromosome-level genome assembly for the angiosperm silene conica |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508779/ https://www.ncbi.nlm.nih.gov/pubmed/37732249 http://dx.doi.org/10.1101/2023.09.05.556365 |
work_keys_str_mv | AT fieldspeterd chromosomelevelgenomeassemblyfortheangiospermsileneconica AT webermelodym chromosomelevelgenomeassemblyfortheangiospermsileneconica AT wanekagus chromosomelevelgenomeassemblyfortheangiospermsileneconica AT brozamandak chromosomelevelgenomeassemblyfortheangiospermsileneconica AT sloandanielb chromosomelevelgenomeassemblyfortheangiospermsileneconica |