Department of Microbiology and Physiological Systems, Program in Immunology and Microbiology, UMassChan Medical School, Worcester, MA.
Department of Immunobiology and Neuroscience, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
J Immunol. 2023 Jun 1;210(11):1804-1814. doi: 10.4049/jimmunol.2100946.
Somatic hypermutation (SHM) is necessary for Ab diversification and involves error-prone DNA repair of activation-induced cytidine deaminase-induced lesions in germinal center (GC) B cells but can also cause genomic instability. GC B cells express low levels of the DNA repair protein apurinic/apyrimidinic (AP) endonuclease (APE)1 and high levels of its homolog APE2. Reduced SHM in APE2-deficient mice suggests that APE2 promotes SHM, but these GC B cells also exhibit reduced proliferation that could impact mutation frequency. In this study, we test the hypothesis that APE2 promotes and APE1 suppresses SHM. We show how APE1/APE2 expression changes in primary murine spleen B cells during activation, impacting both SHM and class-switch recombination (CSR). High levels of both APE1 and APE2 early after activation promote CSR. However, after 2 d, APE1 levels decrease steadily with each cell division, even with repeated stimulation, whereas APE2 levels increase with each stimulation. When GC-level APE1/APE2 expression was engineered by reducing APE1 genetically (apex1+/-) and overexpressing APE2, bona fide activation-induced cytidine deaminase-dependent VDJH4 intron SHM became detectable in primary B cell cultures. The C terminus of APE2 that interacts with proliferating cell nuclear Ag promotes SHM and CSR, although its ATR-Chk1-interacting Zf-GRF domain is not required. However, APE2 does not increase mutations unless APE1 is reduced. Although APE1 promotes CSR, it suppresses SHM, suggesting that downregulation of APE1 in the GC is required for SHM. Genome-wide expression data compare GC and cultured B cells and new models depict how APE1 and APE2 expression and protein interactions change during B cell activation and affect the balance between accurate and error-prone repair during CSR and SHM.
体细胞超突变(SHM)是 Ab 多样性所必需的,涉及激活诱导的胞嘧啶脱氨酶诱导的生发中心(GC)B 细胞中的易错 DNA 修复,但也可导致基因组不稳定。GC B 细胞表达低水平的 DNA 修复蛋白脱嘌呤/脱嘧啶(AP)内切酶(APE)1 和高水平的同源物 APE2。APE2 缺陷小鼠中的 SHM 减少表明 APE2 促进 SHM,但这些 GC B 细胞也表现出减少的增殖,这可能影响突变频率。在这项研究中,我们检验了 APE2 促进和 APE1 抑制 SHM 的假设。我们展示了在激活过程中,初级鼠脾 B 细胞中 APE1/APE2 的表达如何变化,从而影响 SHM 和类别转换重组(CSR)。激活后早期高水平的 APE1 和 APE2 均促进 CSR。然而,在第 2 天,即使进行了重复刺激,APE1 的水平也会随着每个细胞分裂而稳定下降,而 APE2 的水平会随着每次刺激而增加。当通过遗传减少 APE1(apex1+/-)和过表达 APE2 来设计 GC 水平的 APE1/APE2 表达时,在初级 B 细胞培养物中可检测到真正的激活诱导的胞嘧啶脱氨酶依赖性 VDJH4 内含子 SHM。与增殖细胞核 Ag 相互作用的 APE2 的 C 端促进 SHM 和 CSR,尽管其 ATR-Chk1 相互作用的 Zf-GRF 结构域不是必需的。然而,除非 APE1 减少,否则 APE2 不会增加突变。尽管 APE1 促进 CSR,但它抑制 SHM,表明在 GC 中 APE1 的下调是 SHM 所必需的。全基因组表达数据比较了 GC 和培养的 B 细胞,新模型描述了 APE1 和 APE2 的表达和蛋白相互作用如何在 B 细胞激活过程中发生变化,并影响 CSR 和 SHM 过程中准确和易错修复之间的平衡。