Publication date: Available online 24 June 2019
Source: Immunity
Author(s): Danielle A. Chisolm, Wayne Cheng, Shelby A. Colburn, Aaron Silva-Sanchez, Selene Meza-Perez, Troy D. Randall, Amy S. Weinmann
Source: Immunity
Author(s): Danielle A. Chisolm, Wayne Cheng, Shelby A. Colburn, Aaron Silva-Sanchez, Selene Meza-Perez, Troy D. Randall, Amy S. Weinmann
Summary
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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