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一种综合方法,包括CRISPR/Cas9介导的纳米孔测序、配对末端测序和细胞基因组学方法,用于表征急性髓系白血病中的复杂结构重排。

An Integrated Approach Including CRISPR/Cas9-Mediated Nanopore Sequencing, Mate Pair Sequencing, and Cytogenomic Methods to Characterize Complex Structural Rearrangements in Acute Myeloid Leukemia.

作者信息

Phan Michael, Gomes Maria A, Stinnett Victoria, Morsberger Laura, Hoppman Nicole L, Pearce Kathryn E, Smith Kirstin, Phan Brian, Jiang Liqun, Zou Ying S

机构信息

Krieger School of Arts and Sciences, Johns Hopkins University, Baltimore, MD 21205, USA.

Mount Hebron High School, Ellicott City, MD 21042, USA.

出版信息

Biomedicines. 2024 Mar 7;12(3):598. doi: 10.3390/biomedicines12030598.

Abstract

Complex structural chromosome abnormalities such as chromoanagenesis have been reported in acute myeloid leukemia (AML). They are usually not well characterized by conventional genetic methods, and the characterization of chromoanagenesis structural abnormalities from short-read sequencing still presents challenges. Here, we characterized complex structural abnormalities involving chromosomes 2, 3, and 7 in an AML patient using an integrated approach including CRISPR/Cas9-mediated nanopore sequencing, mate pair sequencing (MPseq), and SNP microarray analysis along with cytogenetic methods. SNP microarray analysis revealed chromoanagenesis involving chromosomes 3 and 7, and a pseudotricentric chromosome 7 was revealed by cytogenetic methods. MPseq revealed 138 structural variants (SVs) as putative junctions of complex rearrangements involving chromosomes 2, 3, and 7, which led to 16 novel gene fusions and 33 truncated genes. Thirty CRISPR RNA (crRNA) sequences were designed to map 29 SVs, of which 27 (93.1%) were on-target based on CRISPR/Cas9 crRNA nanopore sequencing. In addition to simple SVs, complex SVs involving over two breakpoints were also revealed. Twenty-one SVs (77.8% of the on-target SVs) were also revealed by MPseq with shared SV breakpoints. Approximately three-quarters of breakpoints were located within genes, especially intronic regions, and one-quarter of breakpoints were intergenic. Alu and LINE repeat elements were frequent among breakpoints. Amplification of the chromosome 7 centromere was also detected by nanopore sequencing. Given the high amplification of the chromosome 7 centromere, extra chromosome 7 centromere sequences (tricentric), and more gains than losses of genomic material, chromoanasynthesis and chromothripsis may be responsible for forming this highly complex structural abnormality. We showed this combination approach's value in characterizing complex structural abnormalities for clinical and research applications. Characterization of these complex structural chromosome abnormalities not only will help understand the molecular mechanisms responsible for the process of chromoanagenesis, but also may identify specific molecular targets and their impact on therapy and overall survival.

摘要

急性髓系白血病(AML)中已报道了诸如染色体混乱等复杂的结构性染色体异常。它们通常无法通过传统遗传学方法得到很好的表征,并且从短读长测序中表征染色体混乱的结构异常仍然存在挑战。在此,我们使用包括CRISPR/Cas9介导的纳米孔测序、配对末端测序(MPseq)、SNP微阵列分析以及细胞遗传学方法在内的综合方法,对一名AML患者中涉及2号、3号和7号染色体的复杂结构异常进行了表征。SNP微阵列分析揭示了涉及3号和7号染色体的染色体混乱,细胞遗传学方法揭示了一条假三着丝粒7号染色体。MPseq揭示了138个结构变异(SVs),作为涉及2号、3号和7号染色体的复杂重排的假定连接点,这导致了16个新的基因融合和33个截短基因。设计了30个CRISPR RNA(crRNA)序列来定位29个SVs,其中基于CRISPR/Cas9 crRNA纳米孔测序,27个(93.1%)命中靶点。除了简单的SVs外,还揭示了涉及两个以上断点的复杂SVs。MPseq也揭示了21个SVs(占命中靶点SVs的77.8%),具有共享的SV断点。大约四分之三的断点位于基因内,尤其是内含子区域,四分之一的断点位于基因间。Alu和LINE重复元件在断点中很常见。纳米孔测序还检测到7号染色体着丝粒的扩增。鉴于7号染色体着丝粒的高度扩增、额外的7号染色体着丝粒序列(三着丝粒)以及基因组物质的增加多于减少,染色体混乱和染色体碎裂可能是形成这种高度复杂结构异常的原因。我们展示了这种联合方法在表征复杂结构异常以用于临床和研究应用方面的价值。表征这些复杂的结构性染色体异常不仅将有助于理解导致染色体混乱过程的分子机制,还可能识别特定的分子靶点及其对治疗和总生存期的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f29/10968562/241d7408927d/biomedicines-12-00598-g001.jpg

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