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Analysis of Somatic Hypermutation in the JH4 intron of Germinal Center B cells from Mouse Peyer's Patches
Published on: April 20, 2021
Apurinic/apyrimidinic endonuclease 1 is the essential nuclease during immunoglobulin class switch recombination
Shahnaz Masani1, Li Han, Kefei Yu
1Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.
Insights
Apurinic/apyrimidinic endonuclease 1 (APE1) is essential for immunoglobulin class switch recombination (CSR). Deleting APE1 in mouse B cells drastically reduced CSR, demonstrating its critical role in DNA cleavage during this process.
Area of Science:
- Immunology
- Molecular Biology
- DNA Repair
Background:
- Immunoglobulin (Ig) class switch recombination (CSR) generates antibody diversity.
- CSR is initiated by activation-induced cytidine deaminase (AID), creating uracils in DNA.
- Uracil processing by repair enzymes leads to DNA double-strand breaks (DSBs) crucial for CSR.
Purpose of the Study:
- To investigate the role of apurinic/apyrimidinic endonuclease 1 (APE1) in CSR.
- To overcome the challenge of embryonic lethality associated with APE1 gene ablation in mice.
- To provide direct evidence for APE1's function in switch region cleavage during CSR.
Main Methods:
- Deletion of the APE1 gene in the CH12F3 mouse B cell line, which supports robust in vitro CSR.
- Assessment of cell viability and growth in APE1-null cells.
- Quantification of CSR efficiency in APE1-deficient cells.
Main Results:
- APE1 gene deletion in CH12F3 cells did not affect cell viability or growth.
- CSR was drastically reduced in APE1-null CH12F3 cells.
- Deletion of AP endonuclease 2 (APE2) had no impact on CSR.
Conclusions:
- APE1 is essential for switch region cleavage and immunoglobulin class switch recombination.
- APE1's role in CSR is demonstrated directly in a viable B cell line.
- APE2 is not required for CSR.
Abstract:
Immunoglobulin (Ig) class switch recombination (CSR) is initiated by activation-induced cytidine deaminase (AID) that catalyzes numerous DNA cytosine deaminations within switch regions. The resulting uracils are processed by uracil base excision and/or mismatch repair enzymes that ultimately generate switch region DNA double-strand breaks (DSBs). Uracil glycosylase 2 (UNG2) is required for CSR, most likely by removing uracils to generate abasic sites. Although it is presumed that the apurinic/apyrimidinic endonuclease 1 (APE1) generates DNA strand incisions (a prerequisite for CSR) at these abasic sites, a direct test of the requirement for APE1 in CSR has been difficult because of the embryonic lethality of APE1 ablation in mice. Here, we report the successful deletion of the APE1 gene in a mouse B cell line (CH12F3) capable of robust CSR in vitro. In contrast to the general assumption that APE1 is essential for cellular viability, deletion of APE1 in CH12F3 cells has no apparent effect on cell viability or growth. Moreover, CSR in APE1-null CH12F3 cells is drastically reduced, providing direct evidence for an essential role for APE1 in switch region cleavage and CSR. Finally, deletion of AP endonuclease 2 (APE2) has no effect on CSR in either APE1-proficient or -deficient cells.
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