Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Blood Adv. 2022 Apr 12;6(7):2275-2289. doi: 10.1182/bloodadvances.2021005703.
Genetic analysis of leukemic clones in monozygotic twins with concordant acute lymphoblastic leukemia (ALL) has proved a unique opportunity to gain insight into the molecular phylogenetics of leukemogenesis. Using whole-genome sequencing, we characterized constitutional and somatic single nucleotide variants/insertion-deletions (indels) and structural variants in a monozygotic twin pair with concordant ETV6-RUNX1+ B-cell precursor ALL (BCP-ALL). In addition, digital PCR (dPCR) was applied to evaluate the presence of and quantify selected somatic variants at birth, diagnosis, and remission. A shared somatic complex rearrangement involving chromosomes 11, 12, and 21 with identical fusion sequences in leukemias of both twins offered direct proof of a common clonal origin. The ETV6-RUNX1 fusion detected at diagnosis was found to originate from this complex rearrangement. A shared somatic frameshift deletion in UBA2 was also identified in diagnostic samples. In addition, each leukemia independently acquired analogous deletions of 3 genes recurrently targeted in BCP-ALLs (ETV6, ATF7IP, and RAG1/RAG2), providing evidence of a convergent clonal evolution only explained by a strong concurrent selective pressure. Quantification of the UBA2 deletion by dPCR surprisingly indicated it persisted in remission. This, for the first time to our knowledge, provided evidence of a UBA2 variant preceding the well-established initiating event ETV6-RUNX1. Further, we suggest the UBA2 deletion exerted a leukemia predisposing effect and that its essential role in Small Ubiquitin-like Modifier (SUMO) attachment (SUMOylation), regulating nearly all physiological and pathological cellular processes such as DNA-repair by nonhomologous end joining, may hold a mechanistic explanation for the predisposition.
同卵双胞胎中一致性急性淋巴细胞白血病(ALL)白血病克隆的遗传分析为深入了解白血病发生的分子系统发生提供了独特的机会。我们使用全基因组测序,对同卵双胞胎中一致性 ETV6-RUNX1+B 细胞前体 ALL(BCP-ALL)的先天和体细胞单核苷酸变异/插入缺失(indels)和结构变异进行了特征描述。此外,还应用数字 PCR(dPCR)在出生时、诊断时和缓解时评估选定的体细胞变异的存在和定量。在双胞胎的白血病中存在涉及染色体 11、12 和 21 的共享体细胞复杂重排,并且融合序列相同,这直接证明了共同的克隆起源。在诊断时发现的 ETV6-RUNX1 融合源自这种复杂的重排。在诊断样本中还发现了 UBA2 的共享体细胞移码缺失。此外,每个白血病独立获得了 BCP-ALL 中经常靶向的 3 个基因的类似缺失(ETV6、ATF7IP 和 RAG1/RAG2),这表明只有在强烈的并发选择性压力下才能解释趋同的克隆进化。dPCR 对 UBA2 缺失的定量令人惊讶地表明它在缓解中持续存在。这是我们首次在知识上提供了 UBA2 变体先于既定起始事件 ETV6-RUNX1 的证据。此外,我们建议 UBA2 缺失具有白血病易感性作用,并且其在小泛素样修饰物(SUMO)附着(SUMOylation)中的基本作用,调节包括非同源末端连接的 DNA 修复在内的几乎所有生理和病理细胞过程,可能为易感性提供机制解释。