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Status |
Public on Apr 13, 2024 |
Title |
Increased AID Results in Mutations at the CRLF2 Locus Implicated in Latin American ALL Health Disparities |
Organism |
Homo sapiens |
Experiment type |
Other
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Summary |
Activation-induced cytidine deaminase (AID) is a B cell-specific base editor required during class switch recombination and somatic hypermutation for B cell maturation and antibody diversification. However, it has also been implicated as a factor in the etiology of several B cell malignancies. Evaluating the AID-induced mutation load in patients at-risk for certain types of blood cancers is critical in assessing disease severity and treatment options. Here, we have developed a digital PCR (dPCR) assay that allows us to track the mutational landscape resulting from AID modification or DNA double-strand break (DSB) formation and repair at sites known to be prone to DSBs. Implementation of this new assay showed that increased AID levels in immature B cells increases genome instability at loci linked to translocation formation. This included the CRLF2 locus that is often involved in chromosomal translocations associated with a subtype of acute lymphoblastic leukemia (ALL) that disproportionately affects Latin Americans (LAs). To support this LA-specific identification of AID mutation signatures, we characterized DNA from immature B cells isolated from the bone marrow of ALL patients. Our ability to detect and quantify these mutation signatures will potentiate future risk identification, early detection of cancers, and reduction of associated cancer health disparities.
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Overall design |
We employed Cas9:IGHM1 and Cas9:IGHM6 gRNA bait DNA double strand break to map translocation and rejoining outcomes in the presence or absence of an additional gRNA targeting cancer gene loci implicated in LatinX populations.
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Web link |
https://www.nature.com/articles/s41467-024-50537-0
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Contributor(s) |
Frock RL, Rangel V, Sterrenberg JN, Pannunzio NR |
Citation(s) |
39068148 |
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Submission date |
Sep 20, 2023 |
Last update date |
Jul 29, 2024 |
Contact name |
Richard L Frock |
E-mail(s) |
frock@stanford.edu
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Organization name |
Stanford University
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Department |
Radiation Oncology
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Lab |
Frock Lab
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Street address |
269 Campus Drive
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City |
Stanford |
State/province |
California |
ZIP/Postal code |
94305 |
Country |
USA |
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Platforms (1) |
GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
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Samples (6)
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Relations |
BioProject |
PRJNA1019358 |