A chromosome-level genome assembly of the bluethroat ( <i>Luscinia s. svecica</i> ; Linnaeus, 1758) uncovers the complex MHC region

Abstract We describe a chromosome-level, pseudo-haplotype-resolved genome assembly from a female bluethroat (Luscinia s. svecica). The assembly comprises two pseudo-haplotypes of 1461 Mb and 1171 Mb, with 77.4% and 88.4% scaffolded into 40 autosomal chromosomes and the W and Z sex chromosomes in pseudo-haplotype one. Assembly completeness is high (BUSCO 99.2% and 94.9%), with 22,462 and 18,769 annotated protein-coding genes for pseudo-haplotypes one and two, respectively. The use of Oxford Nanopore Technologies sequencing enables resolution of genomic regions that are often fragmented in genome assemblies, including the hypervariable Major Histocompatibility Complex (MHC). We find that MHC loci include both the canonical organization of tandemly duplicated MHCIIβ genes with a single MHCIIα, and a distinct arrangement in which MHCI and MHCIIβ loci are interspersed. Substantial structural differences between the two assembled chromosome 35 homologs are resolved across the MHC region.

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Publication Details

Journal
Journal of Heredity
Published
2026-07-22
DOI
https://doi.org/10.1093/jhered/esag058
Primary Topic
T-cell and B-cell Immunology
Type
article
Field-Weighted Citation Impact
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article

A chromosome-level genome assembly of the bluethroat ( Luscinia s. svecica ; Linnaeus, 1758) uncovers the complex MHC region

Morten Skage, Jan Terje Lifjeld, Marius A. Strand, Arild Johnsen et al.
Journal of Heredity
T-cell and B-cell Immunology
article

A chromosome-level genome assembly of the bluethroat ( Luscinia s. svecica ; Linnaeus, 1758) uncovers the complex MHC region

Morten Skage, Jan Terje Lifjeld, Marius A. Strand, Arild Johnsen, Ole K. Tørresen, Erica H. Leder, Giada Ferrari, Ave Tooming-Klunderud, Kjetill S Jakobsen, Emily L G Enevoldsen
article en

Abstract

Abstract We describe a chromosome-level, pseudo-haplotype-resolved genome assembly from a female bluethroat (Luscinia s. svecica). The assembly comprises two pseudo-haplotypes of 1461 Mb and 1171 Mb, with 77.4% and 88.4% scaffolded into 40 autosomal chromosomes and the W and Z sex chromosomes in pseudo-haplotype one. Assembly completeness is high (BUSCO 99.2% and 94.9%), with 22,462 and 18,769 annotated protein-coding genes for pseudo-haplotypes one and two, respectively. The use of Oxford Nanopore Technologies sequencing enables resolution of genomic regions that are often fragmented in genome assemblies, including the hypervariable Major Histocompatibility Complex (MHC). We find that MHC loci include both the canonical organization of tandemly duplicated MHCIIβ genes with a single MHCIIα, and a distinct arrangement in which MHCI and MHCIIβ loci are interspersed. Substantial structural differences between the two assembled chromosome 35 homologs are resolved across the MHC region.

Journal of Heredity
University of Oslo (NO), University of Gothenburg (SE)
Openalex Percentile: Top 14%
T-cell and B-cell Immunology
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