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Evolution of immunogenetic components encoding ultralong CDR H3.
Ott, Jeannine A; Mitchell, Christian; Sheppard, Morgan; Deiss, Thad C; Horton, J M Cody; Haakenson, Jeremy K; Huang, Ruiqi; Kelley, Abigail R; Davis, Brian W; Derr, James N; Smider, Vaughn V; Criscitiello, Michael F.
Afiliación
  • Ott JA; Comparative Immunogenetics Laboratory, Department of Veterinary Pathobiology, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
  • Mitchell C; Comparative Immunogenetics Laboratory, Department of Veterinary Pathobiology, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
  • Sheppard M; Comparative Immunogenetics Laboratory, Department of Veterinary Pathobiology, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
  • Deiss TC; Comparative Immunogenetics Laboratory, Department of Veterinary Pathobiology, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
  • Horton JMC; Department of Veterinary Integrative Sciences, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
  • Haakenson JK; Applied Biomedical Science Institute, San Diego, CA, 92127, USA.
  • Huang R; Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
  • Kelley AR; Applied Biomedical Science Institute, San Diego, CA, 92127, USA.
  • Davis BW; Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
  • Derr JN; Applied Biomedical Science Institute, San Diego, CA, 92127, USA.
  • Smider VV; Department of Veterinary Integrative Sciences, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
  • Criscitiello MF; Comparative Immunogenetics Laboratory, Department of Veterinary Pathobiology, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
Immunogenetics ; 75(4): 323-339, 2023 08.
Article en En | MEDLINE | ID: mdl-37084012
The genomes of most vertebrates contain many V, D, and J gene segments within their Ig loci to construct highly variable CDR3 sequences through combinatorial diversity. This nucleotide variability translates into an antibody population containing extensive paratope diversity. Cattle have relatively few functional VDJ gene segments, requiring innovative approaches for generating diversity like the use of ultralong-encoding IGHV and IGHD gene segments that yield dramatically elongated CDR H3. Unique knob and stalk microdomains create protracted paratopes, where the antigen-binding knob sits atop a long stalk, allowing the antibody to bind both surface and recessed antigen epitopes. We examined genomes of twelve species of Bovidae to determine when ultralong-encoding IGHV and IGHD gene segments evolved. We located the 8-bp duplication encoding the unique TTVHQ motif in ultralong IGHV segments in six Bovid species (cattle, zebu, wild yak, domestic yak, American bison, and domestic gayal), but we did not find evidence of the duplication in species beyond the Bos and Bison genera. Additionally, we analyzed mRNA from bison spleen and identified a rich repertoire of expressed ultralong CDR H3 antibody mRNA, suggesting that bison use ultralong IGHV transcripts in their host defense. We found ultralong-encoding IGHD gene segments in all the same species except domestic yak, but again not beyond the Bos and Bison clade. Thus, the duplication event leading to this ultralong-encoding IGHV gene segment and the emergence of the ultralong-encoding IGHD gene segment appears to have evolved in a common ancestor of the Bos and Bison genera 5-10 million years ago.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bison Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Immunogenetics Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bison Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Immunogenetics Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos