• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

靶向新一代测序可在单个程序中检测点突变、插入、缺失和平衡染色体重排,并鉴定新型白血病特异性融合基因。

Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure.

机构信息

MLL Munich Leukemia Laboratory, Munich, Germany.

出版信息

Leukemia. 2011 Apr;25(4):671-80. doi: 10.1038/leu.2010.309. Epub 2011 Jan 21.

DOI:10.1038/leu.2010.309
PMID:21252984
Abstract

DNA sequence enrichment from complex genomic samples using microarrays enables targeted next-generation sequencing (NGS). In this study, we combined 454 shotgun pyrosequencing with long oligonucleotide sequence capture arrays. We demonstrate the detection of mutations including point mutations, deletions and insertions in a cohort of 22 patients presenting with acute leukemias and myeloid neoplasms. Importantly, this one-step methodological procedure also allowed the detection of balanced chromosomal aberrations, including translocations and inversions. Moreover, the genomic representation of only one of the partner genes of a chimeric fusion on the capture platform also permitted identification of the novel fusion partner genes. Using acute myeloid leukemias harboring RUNX1 abnormalities as a model system, three novel chromosomal fusion sequences and KCNMA1 as a novel RUNX1 fusion partner gene were detected. This assay has the strong potential to become an important method for the comprehensive genetic characterization of particular leukemias and other malignancies harboring complex genomes.

摘要

使用微阵列从复杂基因组样本中进行 DNA 序列富集可实现靶向下一代测序 (NGS)。在这项研究中,我们将 454 焦磷酸测序与长寡核苷酸序列捕获阵列相结合。我们在一组 22 名患有急性白血病和髓系肿瘤的患者中检测到了包括点突变、缺失和插入在内的突变。重要的是,这种一步法方法还允许检测平衡染色体异常,包括易位和倒位。此外,在捕获平台上,即使仅检测到嵌合融合的一个伴侣基因的基因组代表,也可以鉴定出新的融合伴侣基因。我们使用急性髓系白血病作为模型系统,其中 RUNX1 异常,检测到三个新的染色体融合序列和 KCNMA1 作为新的 RUNX1 融合伴侣基因。该检测方法具有成为特定白血病和其他具有复杂基因组的恶性肿瘤的综合遗传特征的重要方法的潜力。

相似文献

1
Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure.靶向新一代测序可在单个程序中检测点突变、插入、缺失和平衡染色体重排,并鉴定新型白血病特异性融合基因。
Leukemia. 2011 Apr;25(4):671-80. doi: 10.1038/leu.2010.309. Epub 2011 Jan 21.
2
Chromosomal aberrations and fusion genes in myeloid malignancies.髓系恶性肿瘤中的染色体异常和融合基因。
Expert Rev Hematol. 2012 Aug;5(4):381-93. doi: 10.1586/ehm.12.30.
3
Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1-PRDM16 fusion in a case of progressive chronic myeloid leukemia: a complex chromosomal rearrangement of underestimated frequency in disease progression?一例进展性慢性髓性白血病中PRDM16和RUNX1的隐匿性及部分缺失,无t(1;21)(p36;q22)和/或RUNX1-PRDM16融合:疾病进展中频率被低估的复杂染色体重排?
Genes Chromosomes Cancer. 2008 Dec;47(12):1110-7. doi: 10.1002/gcc.20611.
4
Whole-exome sequencing of pediatric acute lymphoblastic leukemia.儿科急性淋巴细胞白血病的全外显子组测序。
Leukemia. 2012 Jul;26(7):1602-7. doi: 10.1038/leu.2011.333. Epub 2011 Nov 18.
5
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.骨外黏液样软骨肉瘤中EWS/CHN和RBP56/CHN融合基因的分子遗传学特征
Genes Chromosomes Cancer. 2002 Dec;35(4):340-52. doi: 10.1002/gcc.10127.
6
A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.一例继发性急性髓系白血病中的新型隐匿性易位t(12;17)(p13;p12-p13)导致ETV6基因与PER1基因反义链融合。
Genes Chromosomes Cancer. 2003 May;37(1):79-83. doi: 10.1002/gcc.10175.
7
NUP98 is fused to topoisomerase (DNA) IIbeta 180 kDa (TOP2B) in a patient with acute myeloid leukemia with a new t(3;11)(p24;p15).在一名患有新的t(3;11)(p24;p15)的急性髓系白血病患者中,核孔蛋白98(NUP98)与拓扑异构酶(DNA)IIβ 180千道尔顿(TOP2B)发生融合。
Clin Cancer Res. 2005 Sep 15;11(18):6489-94. doi: 10.1158/1078-0432.CCR-05-0150.
8
Cryptic chromosomal aberrations leading to an AML1/ETO rearrangement are frequently caused by small insertions.导致AML1/ETO重排的隐匿性染色体畸变常由小插入引起。
Genes Chromosomes Cancer. 2003 Mar;36(3):261-72. doi: 10.1002/gcc.10168.
9
Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene.急性白血病中NUP98异常的鉴定:JARID1A(12p13)作为一种新的伙伴基因。
Genes Chromosomes Cancer. 2006 May;45(5):437-46. doi: 10.1002/gcc.20308.
10
ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations.ETV6-NCOA2:急性白血病中的一种新型融合基因,与T淋巴细胞和髓系标志物共表达及频繁的NOTCH1突变相关。
Clin Cancer Res. 2008 Feb 15;14(4):977-83. doi: 10.1158/1078-0432.CCR-07-4022.

引用本文的文献

1
LINC00894, YEATS2-AS1, and SUGP2 genes as novel biomarkers for N0 status of lung adenocarcinoma.LINC00894、YEATS2-AS1和SUGP2基因作为肺腺癌N0状态的新型生物标志物。
Sci Rep. 2025 Mar 27;15(1):10628. doi: 10.1038/s41598-024-84640-5.
2
FACILITATE: A real-world, multicenter, prospective study investigating the utility of a rapid, fully automated real-time PCR assay versus local reference methods for detecting epidermal growth factor receptor variants in NSCLC.促进:一项真实世界、多中心、前瞻性研究,旨在调查一种快速、全自动实时 PCR 检测方法与当地参考方法在检测非小细胞肺癌中表皮生长因子受体变异体的效用。
Pathol Oncol Res. 2023 Jan 31;29:1610707. doi: 10.3389/pore.2023.1610707. eCollection 2023.
3
Seed management using NGS technology to rapidly eliminate a deleterious allele from rice breeder seeds.
利用NGS技术进行种子管理,以快速从水稻育种种子中消除有害等位基因。
Breed Sci. 2022 Dec;72(5):362-371. doi: 10.1270/jsbbs.22058. Epub 2022 Dec 13.
4
Somatic Mutations in Oncogenes Are in Chronic Myeloid Leukemia Acquired Deregulated Base-Excision Repair and Alternative Non-Homologous End Joining.致癌基因中的体细胞突变存在于慢性髓性白血病中,其获得性碱基切除修复失调和替代非同源末端连接。
Front Oncol. 2021 Sep 20;11:744373. doi: 10.3389/fonc.2021.744373. eCollection 2021.
5
Identification of Fusion Gene Breakpoints is Feasible and Facilitates Accurate Sensitive Minimal Residual Disease Monitoring on Genomic Level in Patients With PML-RARA, CBFB-MYH11, and RUNX1-RUNX1T1.融合基因断点的鉴定是可行的,并有助于在PML-RARA、CBFB-MYH11和RUNX1-RUNX1T1患者的基因组水平上进行准确、灵敏的微小残留病监测。
Hemasphere. 2020 Nov 10;4(6):e489. doi: 10.1097/HS9.0000000000000489. eCollection 2020 Dec.
6
Molecular Profiling of Atypical Tenosynovial Giant Cell Tumors Reveals Novel Non- Fusions.非典型腱鞘巨细胞瘤的分子图谱揭示了新的非融合基因。
Cancers (Basel). 2019 Dec 31;12(1):100. doi: 10.3390/cancers12010100.
7
Fast and accurate mutation detection in whole genome sequences of multiple isogenic samples with IsoMut.使用IsoMut对多个同基因样本的全基因组序列进行快速准确的突变检测。
BMC Bioinformatics. 2017 Jan 31;18(1):73. doi: 10.1186/s12859-017-1492-4.
8
SV-STAT accurately detects structural variation via alignment to reference-based assemblies.SV-STAT通过与基于参考的组装进行比对,准确检测结构变异。
Source Code Biol Med. 2016 Jun 18;11:8. doi: 10.1186/s13029-016-0051-0. eCollection 2016.
9
Comprehensive mutation profiling by next-generation sequencing of effusion fluids from patients with high-grade serous ovarian carcinoma.通过对高级别浆液性卵巢癌患者的积液进行下一代测序进行全面的突变分析。
Cancer Cytopathol. 2015 May;123(5):289-97. doi: 10.1002/cncy.21522. Epub 2015 Feb 5.
10
Recombination in viruses: mechanisms, methods of study, and evolutionary consequences.病毒中的重组:机制、研究方法及进化后果
Infect Genet Evol. 2015 Mar;30:296-307. doi: 10.1016/j.meegid.2014.12.022. Epub 2014 Dec 23.