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利用DNA修复机制的见解来发现微同源性介导的末端连接缺失和新机制。

Utilizing insights of DNA repair machinery to discover MMEJ deletions and novel mechanisms.

作者信息

Kadam Aditee, Shilo Shay, Naor Hadas, Wainstein Alexander, Brilon Yardena, Feldman Tzah, Minden Mark, Kaushansky Nathali, Chapal-Ilani Noa, Shlush Liran

机构信息

Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 761001, Israel.

Sequentify Ltd., 10 Moti Kind St., 5th Floor, Rehovot 7638519, Israel.

出版信息

Nucleic Acids Res. 2024 Dec 11;52(22):e106. doi: 10.1093/nar/gkae1132.

DOI:10.1093/nar/gkae1132
PMID:39607705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11662932/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/e2244d851785/gkae1132fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/7b5baf3d290a/gkae1132figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/29603d87b012/gkae1132fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/88426a7ee175/gkae1132fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/53e73b317e2d/gkae1132fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/e2244d851785/gkae1132fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/7b5baf3d290a/gkae1132figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/29603d87b012/gkae1132fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/88426a7ee175/gkae1132fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/53e73b317e2d/gkae1132fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eeb/11662932/e2244d851785/gkae1132fig4.jpg

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本文引用的文献

1
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NAR Genom Bioinform. 2022 Sep 5;4(3):lqac063. doi: 10.1093/nargab/lqac063. eCollection 2022 Sep.
2
The complete sequence of a human genome.人类基因组的完整序列。
Science. 2022 Apr;376(6588):44-53. doi: 10.1126/science.abj6987. Epub 2022 Mar 31.
3
Tool evaluation for the detection of variably sized indels from next generation whole genome and targeted sequencing data.工具评估用于检测下一代全基因组和靶向测序数据中的可变大小插入缺失。
PLoS Comput Biol. 2022 Feb 17;18(2):e1009269. doi: 10.1371/journal.pcbi.1009269. eCollection 2022 Feb.
4
Pangenomics enables genotyping of known structural variants in 5202 diverse genomes.泛基因组学能够对 5202 个不同基因组中的已知结构变异进行基因分型。
Science. 2021 Dec 17;374(6574):abg8871. doi: 10.1126/science.abg8871.
5
To Join or Not to Join: Decision Points Along the Pathway to Double-Strand Break Repair vs. Chromosome End Protection.加入还是不加入:双链断裂修复与染色体末端保护途径中的决策点
Front Cell Dev Biol. 2021 Jul 12;9:708763. doi: 10.3389/fcell.2021.708763. eCollection 2021.
6
Recurrent deletions in clonal hematopoiesis are driven by microhomology-mediated end joining.克隆性造血中的反复缺失是由微同源介导的末端连接驱动的。
Nat Commun. 2021 Apr 28;12(1):2455. doi: 10.1038/s41467-021-22803-y.
7
Repair of DNA Double-Strand Breaks by the Nonhomologous End Joining Pathway.非同源末端连接途径修复 DNA 双链断裂。
Annu Rev Biochem. 2021 Jun 20;90:137-164. doi: 10.1146/annurev-biochem-080320-110356. Epub 2021 Feb 8.
8
Identifying genetic variants underlying phenotypic variation in plants without complete genomes.鉴定没有完整基因组的植物表型变异的遗传变异。
Nat Genet. 2020 May;52(5):534-540. doi: 10.1038/s41588-020-0612-7. Epub 2020 Apr 13.
9
The repertoire of mutational signatures in human cancer.人类癌症中的突变特征谱。
Nature. 2020 Feb;578(7793):94-101. doi: 10.1038/s41586-020-1943-3. Epub 2020 Feb 5.
10
Comprehensive evaluation and characterisation of short read general-purpose structural variant calling software.全面评估和特征分析短读通用结构变异调用软件。
Nat Commun. 2019 Jul 19;10(1):3240. doi: 10.1038/s41467-019-11146-4.