| Literature DB >> 31248780 |
Danielle A Chisolm1, Wayne Cheng1, Shelby A Colburn1, Aaron Silva-Sanchez2, Selene Meza-Perez2, Troy D Randall2, Amy S Weinmann3.
Abstract
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.Entities:
Keywords: CD45.1; CD8(+) T cells; Cxcr4; ERV; Ly5.1; Rgs16; T-bet; Tfh; Th1; germ-free
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Year: 2019 PMID: 31248780 PMCID: PMC6883924 DOI: 10.1016/j.immuni.2019.05.006
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745