Kadam Aditee, Shilo Shay, Naor Hadas, Wainstein Alexander, Brilon Yardena, Feldman Tzah, Minden Mark, Kaushansky Nathali, Chapal-Ilani Noa, Shlush Liran
Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 761001, Israel.
Sequentify Ltd., 10 Moti Kind St., 5th Floor, Rehovot 7638519, Israel.
Nucleic Acids Res. 2024 Dec 11;52(22):e106. doi: 10.1093/nar/gkae1132.
We developed Del-read, an algorithm targeting medium-sized deletions (6-100 bp) in short-reads, which are challenging for current variant callers relying on alignment. Our focus was on Micro-Homolog mediated End Joining deletions (MMEJ-dels), prevalent in myeloid malignancies. MMEJ-dels follow a distinct pattern, occurring between two homologies, allowing us to generate a comprehensive list of MMEJ-dels in the exome. Using Del-read, we identified numerous novel germline and somatic MMEJ-dels in BEAT-AML and TCGA-breast datasets. Validation in 672 healthy individuals confirmed their presence. These novel MMEJ-dels were linked to genomic features associated with replication stress, like G-quadruplexes and minisatellite. Additionally, we observed a new category of MMEJ-dels with an imperfect-match at the flanking sequences of the homologies, suggesting a mechanism involving mispairing in homology alignment. We demonstrated robustness of the repair system despite CRISPR/Cas9-induced mismatches in the homologies. Further analysis of the canonical ASXL1 deletion revealed a diverse array of these imperfect-matches. This suggests a potentially more flexible and error-prone MMEJ repair system than previously understood. Our findings highlight Del-read's potential in uncovering previously undetected deletions and deepen our understanding of repair mechanisms.
我们开发了Del-read,这是一种针对短读长中6至100个碱基对的中等大小缺失的算法,对于当前依赖比对的变异检测工具来说,检测此类缺失颇具挑战。我们关注的是髓系恶性肿瘤中普遍存在的微同源介导末端连接缺失(MMEJ-dels)。MMEJ-dels遵循一种独特的模式,发生在两个同源序列之间,这使我们能够生成外显子组中MMEJ-dels的完整列表。使用Del-read,我们在BEAT-AML和TCGA乳腺癌数据集中鉴定出了大量新的种系和体细胞MMEJ-dels。在672名健康个体中的验证证实了它们的存在。这些新的MMEJ-dels与诸如G-四链体和微卫星等与复制应激相关的基因组特征有关。此外,我们观察到一类新的MMEJ-dels,其同源序列侧翼存在不完全匹配,这表明存在一种涉及同源比对中错配的机制。尽管CRISPR/Cas9在同源序列中诱导了错配,我们仍证明了修复系统的稳健性。对典型的ASXL1缺失的进一步分析揭示了这些不完全匹配的多样性。这表明MMEJ修复系统可能比之前认为的更灵活且更容易出错。我们的研究结果突出了Del-read在发现先前未检测到的缺失方面的潜力,并加深了我们对修复机制的理解。