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The Functional Genomics Core (FGC) is established under the leadership of Vanderbilt Center for Immunobiology (VCI). By providing services using pooled CRISPR screening technology, FGC is expected to connect specific genes with disease in mouse models and human patient samples, eventually to facilitate the identification of therapeutic targets. 

 

iLab Link to request services: https://vumc.corefacilities.org/service_center/4767?tab=about

 

FGC1     

FGC 2

An unbiased in vivo CRISPR screening in primary murine T cells identified MTHFD2 as a hit that was also upregulated consistently in individuals with inflammatory disorders. Notably, MTHFD2 deficiency impaired Teff cell proliferation and function [1].

 

FGC3  

 

FGC4

In vitro and in vivo CRISPR screens used to assay functional drivers of inborn errors of immunity and metabolism identified multiple metabolic mechanisms responsible for defects [2].

 

References to images

  1. Sugiura, Ayaka, et al. "MTHFD2 is a metabolic checkpoint controlling effector and regulatory T cell fate and function." Immunity 55.1 (2022): 65-81.
  2. Patterson, Andrew R., et al. "Functional Overlap of Inborn Errors of Immunity and Metabolism Genes Define T Cell Immunometabolic Vulnerabilities." bioRxiv (2023): 2023-01.
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