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Immunity ; 51(1): 155-168.e5, 2019 07 16.
Artículo en Inglés | MEDLINE | ID: mdl-31248780

RESUMEN

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.


Asunto(s)
Catepsina E/metabolismo , Elementos de Facilitación Genéticos/genética , Inmunidad/genética , Receptores CXCR4/metabolismo , Células TH1/inmunología , Animales , Catepsina E/genética , Comercio , Regulación de la Expresión Génica , Antecedentes Genéticos , Variación Genética , Centro Germinal/inmunología , Secuenciación de Nucleótidos de Alto Rendimiento , Endogamia , Antígenos Comunes de Leucocito/genética , Ratones , Ratones Congénicos , Ratones Endogámicos C57BL , Modelos Animales , Receptores CXCR4/genética
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