Genome-wide CRISPR screening of chondrocyte maturation newly implicates genes in skeletal growth and height-associated GWAS loci

Baronas, John; Bartell, Eric; Eliasen, Anders U.; Doench, John G.; Yengo, Loïc; Vedantam, Sailaja; Marouli, Eirini; Kronenberg, Henry M.; Hirschhorn, Joel N.; Renthal, Nora E.

doi:10.1016/j.xgen.2023.100299

Cited by 9 publications

(1 citation statement)

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“…However, identifying the target gene(s) at a locus, which has been done for less than 20 loci by chromatin conformation analysis and luciferase assays [44][45][46][47] , is time consuming and does not address the issue of molecular pleiotropy: it is important to know which target gene(s) can impact on a phenotype relevant to the disease or trait of interest. To complement studies of individual risk loci, pooled functional screens for follow up of GWAS findings for coronary artery disease, lung disease, blood traits, type 2 diabetes and height [48][49][50][51][52] . We have undertaken functional CRISPR screens to enable the identification of genes near GWAS signals that impact the hallmarks of cancer.…”

Section: Discussionmentioning

confidence: 99%

Pooled genetic screens identify breast cancer risk genes involved in evasion from T cell-mediated killing

Shi,

Luo,

Burrows

et al. 2024

Preprint

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Genome-wide association studies have identified more than 220 loci associated with breast cancer susceptibility. A major challenge is now to identify the effector genes with plausible functions in the context of breast cancer risk. We have previously performed pooled CRISPR screens to identify target genes at risk loci that drive cancer hallmarks including proliferation or modulating DNA damage response. We now extend these screens to identify genes involved in response to cytotoxic T lymphocyte (CTL) killing. We performed knockout and inhibition screens to identify genes that affect the response of the MCF7 human breast cancer cell line to CTL killing in anin vitroco-culture system. We identified 33 candidate risk genes associated with resistance or sensitisation to T cell-mediated killing. Using single gene perturbation, we showed that deletion of candidate risk genesIRF1, ATF7IP, CCDC170andCASP8induced resistance, while ablation ofCFLAR, CREBBP, andPRMT7sensitized cells to CTL killing. We used reporter assays to show that the risk-associated alleles at rs736801 and rs3769821 reduced transactivation of theIRF1andCASP8promoters, respectively. We showed that pharmacological inhibition of PRMT7 rendered breast cells sensitive to CTL killing andPRMT7levels were negatively correlated with CD8+ infiltration and patient survival in luminal A breast cancer patient cohorts. Our results demonstrate that phenotypic pooled CRISPR screens are a useful approach for high throughput functional follow-up of GWAS findings, identifying genes which alter immune responses to breast cancer which offer opportunities to enhance immunotherapy.

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