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Chromosome-level genome assembly of the blue crab, Callinectes sapidus
The blue crab, Callinectes sapidus (Rathbun, 1896) is an economically, culturally, and ecologically important species found across the temperate and tropical North and South American Atlantic coast. A reference genome will enable research for this high-value species. Initial assembly combined 200× c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496215/ https://www.ncbi.nlm.nih.gov/pubmed/34544121 http://dx.doi.org/10.1093/g3journal/jkab212 |
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author | Bachvaroff, Tsvetan R McDonald, Ryan C Plough, Louis V Chung, J Sook |
author_facet | Bachvaroff, Tsvetan R McDonald, Ryan C Plough, Louis V Chung, J Sook |
author_sort | Bachvaroff, Tsvetan R |
collection | PubMed |
description | The blue crab, Callinectes sapidus (Rathbun, 1896) is an economically, culturally, and ecologically important species found across the temperate and tropical North and South American Atlantic coast. A reference genome will enable research for this high-value species. Initial assembly combined 200× coverage Illumina paired-end reads, a 60× 8 kb mate-paired library, and 50× PacBio data using the MaSuRCA assembler resulting in a 985 Mb assembly with a scaffold N50 of 153 kb. Dovetail Chicago and HiC sequencing with the 3d DNA assembler and Juicebox assembly tools were then used for chromosome scaffolding. The 50 largest scaffolds span 810 Mb are 1.5–37 Mb long and have a repeat content of 36%. The 190 Mb unplaced sequence is in 3921 sequences over 10 kb with a repeat content of 68%. The final assembly N50 is 18.9 Mb for scaffolds and 9317 bases for contigs. Of arthropod BUSCO, ∼88% (888/1013) were complete and single copies. Using 309 million RNAseq read pairs from 12 different tissues and developmental stages, 25,249 protein-coding genes were predicted. Between C. sapidus and Portunus trituberculatus genomes, 41 of 50 large scaffolds had high nucleotide identity and protein-coding synteny, but 9 scaffolds in both assemblies were not clear matches. The protein-coding genes included 9423 one-to-one putative orthologs, of which 7165 were syntenic between the two crab species. Overall, the two crab genome assemblies show strong similarities at the nucleotide, protein, and chromosome level and verify the blue crab genome as an excellent reference for this important seafood species. |
format | Online Article Text |
id | pubmed-8496215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84962152021-10-07 Chromosome-level genome assembly of the blue crab, Callinectes sapidus Bachvaroff, Tsvetan R McDonald, Ryan C Plough, Louis V Chung, J Sook G3 (Bethesda) Genome Report The blue crab, Callinectes sapidus (Rathbun, 1896) is an economically, culturally, and ecologically important species found across the temperate and tropical North and South American Atlantic coast. A reference genome will enable research for this high-value species. Initial assembly combined 200× coverage Illumina paired-end reads, a 60× 8 kb mate-paired library, and 50× PacBio data using the MaSuRCA assembler resulting in a 985 Mb assembly with a scaffold N50 of 153 kb. Dovetail Chicago and HiC sequencing with the 3d DNA assembler and Juicebox assembly tools were then used for chromosome scaffolding. The 50 largest scaffolds span 810 Mb are 1.5–37 Mb long and have a repeat content of 36%. The 190 Mb unplaced sequence is in 3921 sequences over 10 kb with a repeat content of 68%. The final assembly N50 is 18.9 Mb for scaffolds and 9317 bases for contigs. Of arthropod BUSCO, ∼88% (888/1013) were complete and single copies. Using 309 million RNAseq read pairs from 12 different tissues and developmental stages, 25,249 protein-coding genes were predicted. Between C. sapidus and Portunus trituberculatus genomes, 41 of 50 large scaffolds had high nucleotide identity and protein-coding synteny, but 9 scaffolds in both assemblies were not clear matches. The protein-coding genes included 9423 one-to-one putative orthologs, of which 7165 were syntenic between the two crab species. Overall, the two crab genome assemblies show strong similarities at the nucleotide, protein, and chromosome level and verify the blue crab genome as an excellent reference for this important seafood species. Oxford University Press 2021-06-18 /pmc/articles/PMC8496215/ /pubmed/34544121 http://dx.doi.org/10.1093/g3journal/jkab212 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Genome Report Bachvaroff, Tsvetan R McDonald, Ryan C Plough, Louis V Chung, J Sook Chromosome-level genome assembly of the blue crab, Callinectes sapidus |
title | Chromosome-level genome assembly of the blue crab, Callinectes sapidus |
title_full | Chromosome-level genome assembly of the blue crab, Callinectes sapidus |
title_fullStr | Chromosome-level genome assembly of the blue crab, Callinectes sapidus |
title_full_unstemmed | Chromosome-level genome assembly of the blue crab, Callinectes sapidus |
title_short | Chromosome-level genome assembly of the blue crab, Callinectes sapidus |
title_sort | chromosome-level genome assembly of the blue crab, callinectes sapidus |
topic | Genome Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496215/ https://www.ncbi.nlm.nih.gov/pubmed/34544121 http://dx.doi.org/10.1093/g3journal/jkab212 |
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