GENYO. Centre for Genomics and Oncological Research: Pfizer / University of Granada / Andalusian Regional Government, PTS Granada - Avenida de la Ilustración 114, Granada, 18016, Spain.
Health Research Institute of Granada (Ibs.Granada), Avenida de Madrid 15, Granada, 18012, Spain.
Mol Cancer. 2024 Feb 24;23(1):42. doi: 10.1186/s12943-024-01960-w.
Diffuse large B-cell lymphoma (DLBCL) is the most common lymphoma. A major mutagenic process in DLBCL is aberrant somatic hypermutation (aSHM) by activation-induced cytidine deaminase (AID), which occurs preferentially at RCH/TW sequence motifs proximal to transcription start sites. Splice sequences are highly conserved, rich in RCH/TW motifs, and recurrently mutated in DLBCL. Therefore, we hypothesized that aSHM may cause recurrent splicing mutations in DLBCL. In a meta-cohort of > 1,800 DLBCLs, we found that 77.5% of splicing mutations in 29 recurrently mutated genes followed aSHM patterns. In addition, in whole-genome sequencing (WGS) data from 153 DLBCLs, proximal mutations in splice sequences, especially in donors, were significantly enriched in RCH/TW motifs (p < 0.01). We validated this enrichment in two additional DLBCL cohorts (N > 2,000; p < 0.0001) and confirmed its absence in 12 cancer types without aSHM (N > 6,300). Comparing sequencing data from mouse models with and without AID activity showed that the splice donor sequences were the top genomic feature enriched in AID-induced mutations (p < 0.0001). Finally, we observed that most AID-related splice site mutations are clonal within a sample, indicating that aSHM may cause early loss-of-function events in lymphomagenesis. Overall, these findings support that AID causes an overrepresentation of clonal splicing mutations in DLBCL.
弥漫性大 B 细胞淋巴瘤(DLBCL)是最常见的淋巴瘤。在 DLBCL 中,一种主要的诱变过程是激活诱导的胞嘧啶脱氨酶(AID)引起的异常体细胞超突变(aSHM),它优先发生在靠近转录起始位点的 RCH/TW 序列基序附近。剪接序列高度保守,富含 RCH/TW 基序,并且在 DLBCL 中经常发生突变。因此,我们假设 aSHM 可能导致 DLBCL 中反复出现的剪接突变。在一个包含>1800 例 DLBCL 的元队列中,我们发现 29 个反复突变基因中的 77.5%的剪接突变遵循 aSHM 模式。此外,在来自 153 例 DLBCL 的全基因组测序(WGS)数据中,在剪接序列中靠近的突变,特别是在供体中,在 RCH/TW 基序中显著富集(p<0.01)。我们在另外两个 DLBCL 队列(N>2000;p<0.0001)中验证了这种富集,并在没有 aSHM 的 12 种癌症类型(N>6300)中证实了其不存在。比较具有和不具有 AID 活性的小鼠模型的测序数据表明,剪接供体序列是 AID 诱导的突变中富集的最高基因组特征(p<0.0001)。最后,我们观察到大多数与 AID 相关的剪接位点突变在一个样本内是克隆的,这表明 aSHM 可能在淋巴瘤发生早期导致功能丧失事件。总的来说,这些发现支持 AID 在 DLBCL 中导致克隆剪接突变的过度表达。