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A Nanopore Based Chromosome-Level Assembly Representing Atlantic Cod from the Celtic Sea

Currently available genome assemblies for Atlantic cod (Gadus morhua) have been constructed from fish belonging to the Northeast Arctic Cod (NEAC) population; a migratory population feeding in the Barents Sea. These assemblies have been crucial for the development of genetic markers which have been...

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Autores principales: Kirubakaran, Tina Graceline, Andersen, Øivind, Moser, Michel, Árnyasi, Mariann, McGinnity, Philip, Lien, Sigbjørn, Kent, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466986/
https://www.ncbi.nlm.nih.gov/pubmed/32641450
http://dx.doi.org/10.1534/g3.120.401423
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author Kirubakaran, Tina Graceline
Andersen, Øivind
Moser, Michel
Árnyasi, Mariann
McGinnity, Philip
Lien, Sigbjørn
Kent, Matthew
author_facet Kirubakaran, Tina Graceline
Andersen, Øivind
Moser, Michel
Árnyasi, Mariann
McGinnity, Philip
Lien, Sigbjørn
Kent, Matthew
author_sort Kirubakaran, Tina Graceline
collection PubMed
description Currently available genome assemblies for Atlantic cod (Gadus morhua) have been constructed from fish belonging to the Northeast Arctic Cod (NEAC) population; a migratory population feeding in the Barents Sea. These assemblies have been crucial for the development of genetic markers which have been used to study population differentiation and adaptive evolution in Atlantic cod, pinpointing four discrete islands of genomic divergence located on linkage groups 1, 2, 7 and 12. In this paper, we present a high-quality reference genome from a male Atlantic cod representing a southern population inhabiting the Celtic sea. The genome assembly (gadMor_Celtic) was produced from long-read nanopore data and has a combined contig length of 686 Mb with an N50 of 10 Mb. Integrating contigs with genetic linkage mapping information enabled us to construct 23 chromosome sequences which mapped with high confidence to the latest NEAC population assembly (gadMor3) and allowed us to characterize, to an extent not previously reported large chromosomal inversions on linkage groups 1, 2, 7 and 12. In most cases, inversion breakpoints could be located within single nanopore contigs. Our results suggest the presence of inversions in Celtic cod on linkage groups 6, 11 and 21, although these remain to be confirmed. Further, we identified a specific repetitive element that is relatively enriched at predicted centromeric regions. Our gadMor_Celtic assembly provides a resource representing a ‘southern’ cod population which is complementary to the existing ‘northern’ population based genome assemblies and represents the first step toward developing pan-genomic resources for Atlantic cod.
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spelling pubmed-74669862020-09-14 A Nanopore Based Chromosome-Level Assembly Representing Atlantic Cod from the Celtic Sea Kirubakaran, Tina Graceline Andersen, Øivind Moser, Michel Árnyasi, Mariann McGinnity, Philip Lien, Sigbjørn Kent, Matthew G3 (Bethesda) Genome Report Currently available genome assemblies for Atlantic cod (Gadus morhua) have been constructed from fish belonging to the Northeast Arctic Cod (NEAC) population; a migratory population feeding in the Barents Sea. These assemblies have been crucial for the development of genetic markers which have been used to study population differentiation and adaptive evolution in Atlantic cod, pinpointing four discrete islands of genomic divergence located on linkage groups 1, 2, 7 and 12. In this paper, we present a high-quality reference genome from a male Atlantic cod representing a southern population inhabiting the Celtic sea. The genome assembly (gadMor_Celtic) was produced from long-read nanopore data and has a combined contig length of 686 Mb with an N50 of 10 Mb. Integrating contigs with genetic linkage mapping information enabled us to construct 23 chromosome sequences which mapped with high confidence to the latest NEAC population assembly (gadMor3) and allowed us to characterize, to an extent not previously reported large chromosomal inversions on linkage groups 1, 2, 7 and 12. In most cases, inversion breakpoints could be located within single nanopore contigs. Our results suggest the presence of inversions in Celtic cod on linkage groups 6, 11 and 21, although these remain to be confirmed. Further, we identified a specific repetitive element that is relatively enriched at predicted centromeric regions. Our gadMor_Celtic assembly provides a resource representing a ‘southern’ cod population which is complementary to the existing ‘northern’ population based genome assemblies and represents the first step toward developing pan-genomic resources for Atlantic cod. Genetics Society of America 2020-07-08 /pmc/articles/PMC7466986/ /pubmed/32641450 http://dx.doi.org/10.1534/g3.120.401423 Text en Copyright © 2020 Kirubakaran et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Report
Kirubakaran, Tina Graceline
Andersen, Øivind
Moser, Michel
Árnyasi, Mariann
McGinnity, Philip
Lien, Sigbjørn
Kent, Matthew
A Nanopore Based Chromosome-Level Assembly Representing Atlantic Cod from the Celtic Sea
title A Nanopore Based Chromosome-Level Assembly Representing Atlantic Cod from the Celtic Sea
title_full A Nanopore Based Chromosome-Level Assembly Representing Atlantic Cod from the Celtic Sea
title_fullStr A Nanopore Based Chromosome-Level Assembly Representing Atlantic Cod from the Celtic Sea
title_full_unstemmed A Nanopore Based Chromosome-Level Assembly Representing Atlantic Cod from the Celtic Sea
title_short A Nanopore Based Chromosome-Level Assembly Representing Atlantic Cod from the Celtic Sea
title_sort nanopore based chromosome-level assembly representing atlantic cod from the celtic sea
topic Genome Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466986/
https://www.ncbi.nlm.nih.gov/pubmed/32641450
http://dx.doi.org/10.1534/g3.120.401423
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