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Resolving haplotype variation and complex genetic architecture in the human immunoglobulin kappa chain locus in individuals of diverse ancestry.
Engelbrecht, Eric; Rodriguez, Oscar L; Shields, Kaitlyn; Schultze, Steven; Tieri, David; Jana, Uddalok; Yaari, Gur; Lees, William D; Smith, Melissa L; Watson, Corey T.
Afiliação
  • Engelbrecht E; Department of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY, USA.
  • Rodriguez OL; Department of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY, USA.
  • Shields K; Department of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY, USA.
  • Schultze S; Department of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY, USA.
  • Tieri D; Department of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY, USA.
  • Jana U; Department of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY, USA.
  • Yaari G; Faculty of Engineering, Bar Ilan University, Ramat Gan, Israel.
  • Lees WD; Institute of Nanotechnology and Advanced Materials, Bar Ilan University, Ramat Gan, Israel.
  • Smith ML; Faculty of Engineering, Bar Ilan University, Ramat Gan, Israel.
  • Watson CT; Department of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY, USA. ml.smith@louisville.edu.
Genes Immun ; 2024 Jun 06.
Article em En | MEDLINE | ID: mdl-38844673
ABSTRACT
Immunoglobulins (IGs), critical components of the human immune system, are composed of heavy and light protein chains encoded at three genomic loci. The IG Kappa (IGK) chain locus consists of two large, inverted segmental duplications. The complexity of the IG loci has hindered use of standard high-throughput methods for characterizing genetic variation within these regions. To overcome these limitations, we use long-read sequencing to create haplotype-resolved IGK assemblies in an ancestrally diverse cohort (n = 36), representing the first comprehensive description of IGK haplotype variation. We identify extensive locus polymorphism, including novel single nucleotide variants (SNVs) and novel structural variants harboring functional IGKV genes. Among 47 functional IGKV genes, we identify 145 alleles, 67 of which were not previously curated. We report inter-population differences in allele frequencies for 10 IGKV genes, including alleles unique to specific populations within this dataset. We identify haplotypes carrying signatures of gene conversion that associate with SNV enrichment in the IGK distal region, and a haplotype with an inversion spanning the proximal and distal regions. These data provide a critical resource of curated genomic reference information from diverse ancestries, laying a foundation for advancing our understanding of population-level genetic variation in the IGK locus.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genes Immun Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genes Immun Ano de publicação: 2024 Tipo de documento: Article