Title | Multiplexed Functional Assessment of Genetic Variants in CARD11. |
Publication Type | Journal Article |
Year of Publication | 2020 |
Authors | Meitlis, I, Allenspach, EJ, Bauman, BM, Phan, IQ, Dabbah, G, Schmitt, EG, Camp, ND, Torgerson, TR, Nickerson, DA, Bamshad, MJ, Hagin, D, Luthers, CR, Stinson, JR, Gray, J, Lundgren, I, Church, JA, Butte, MJ, Jordan, MB, Aceves, SS, Schwartz, DM, Milner, JD, Schuval, S, Skoda-Smith, S, Cooper, MA, Starita, LM, Rawlings, DJ, Snow, AL, James, RG |
Journal | Am J Hum Genet |
Volume | 107 |
Issue | 6 |
Pagination | 1029-1043 |
Date Published | 2020 12 03 |
ISSN | 1537-6605 |
Keywords | Adenine, B-Cell CLL-Lymphoma 10 Protein, B-Lymphocytes, CARD Signaling Adaptor Proteins, Cell Line, Diploidy, Exons, Genes, Dominant, Genetic Variation, Guanylate Cyclase, Humans, Immunologic Deficiency Syndromes, Jurkat Cells, Lymphoma, NF-kappa B p50 Subunit, Piperidines, Polymorphism, Single Nucleotide, Primary Immunodeficiency Diseases, Sensitivity and Specificity |
Abstract | Genetic testing has increased the number of variants identified in disease genes, but the diagnostic utility is limited by lack of understanding variant function. CARD11 encodes an adaptor protein that expresses dominant-negative and gain-of-function variants associated with distinct immunodeficiencies. Here, we used a "cloning-free" saturation genome editing approach in a diploid cell line to simultaneously score 2,542 variants for decreased or increased function in the region of CARD11 associated with immunodeficiency. We also described an exon-skipping mechanism for CARD11 dominant-negative activity. The classification of reported clinical variants was sensitive (94.6%) and specific (88.9%), which rendered the data immediately useful for interpretation of seven coding and splicing variants implicated in immunodeficiency found in our clinic. This approach is generalizable for variant interpretation in many other clinically actionable genes, in any relevant cell type. |
DOI | 10.1016/j.ajhg.2020.10.015 |
Alternate Journal | Am J Hum Genet |
PubMed ID | 33202260 |
PubMed Central ID | PMC7820631 |
Grant List | R01 CA201135 / CA / NCI NIH HHS / United States RM1 HG010461 / HG / NHGRI NIH HHS / United States U54 AI082973 / AI / NIAID NIH HHS / United States UM1 HG006493 / HG / NHGRI NIH HHS / United States |