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Defining Genetic Variation in Widely Used Congenic and Backcrossed Mouse Models Reveals Varied Regulation of Genes Important for Immune Responses.
Chisolm, Danielle A; Cheng, Wayne; Colburn, Shelby A; Silva-Sanchez, Aaron; Meza-Perez, Selene; Randall, Troy D; Weinmann, Amy S.
Afiliação
  • Chisolm DA; Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Cheng W; Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Colburn SA; Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Silva-Sanchez A; Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Meza-Perez S; Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Randall TD; Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Weinmann AS; Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address: weinmann@uab.edu.
Immunity ; 51(1): 155-168.e5, 2019 07 16.
Article em En | MEDLINE | ID: mdl-31248780
Genetic variation influences how the genome is interpreted in individuals and in mouse strains used to model immune responses. We developed approaches to utilize next-generation sequencing datasets to identify sequence variation in genes and enhancer elements in congenic and backcross mouse models. We defined genetic variation in the widely used B6-CD45.2 and B6.SJL-CD45.1 congenic model, identifying substantial differences in SJL genetic content retained in B6.SJL-CD45.1 strains on the basis of the vendor source of the mice. Genes encoding PD-1, CD62L, Bcl-2, cathepsin E, and Cxcr4 were within SJL genetic content in at least one vendor source of B6.SJL-CD45.1 mice. SJL genetic content affected enhancer elements, gene regulation, protein expression, and amino acid content in CD4+ T helper 1 cells, and mice infected with influenza showed reduced expression of Cxcr4 on B6.SJL-CD45.1 T follicular helper cells. These findings provide information on experimental variables and aid in creating approaches that account for genetic variables.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Elementos Facilitadores Genéticos / Células Th1 / Receptores CXCR4 / Catepsina E / Imunidade Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Elementos Facilitadores Genéticos / Células Th1 / Receptores CXCR4 / Catepsina E / Imunidade Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article