• 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

采用分子细胞遗传学技术,在照射前后对 293 细胞中基因座和区域特异性易位的新型断点进行鉴定。

Identification of novel breakpoints for locus- and region-specific translocations in 293 cells by molecular cytogenetics before and after irradiation.

机构信息

Division of Radiation Health, Department of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

Myeloma Center, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

出版信息

Sci Rep. 2019 Jul 22;9(1):10554. doi: 10.1038/s41598-019-47002-0.

DOI:10.1038/s41598-019-47002-0
PMID:31332273
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6646394/
Abstract

The human kidney embryonic 293 cell line (293 cells) is extensively used in biomedical and pharmaceutical research. These cells exhibit a number of numerical and structural chromosomal anomalies. However, the breakpoints responsible for these structural chromosomal rearrangements have not been comprehensively characterized. In addition, it is not known whether chromosomes with structural rearrangement are more sensitive to external toxic agents, such as ionizing radiation. We used G-banding, spectral karyotyping (SKY), and locus- and region-specific fluorescence in situ hybridization (FISH) probes designed in our lab or obtained from commercial vendor to address this gap. Our G-banding analysis revealed that the chromosome number varies from 66 to 71, with multiple rearrangements and partial additions and deletions. SKY analysis confirmed 3 consistent rearrangements, two simple and one complex in nature. Multicolor FISH analysis identified an array of breakpoints responsible for locus- and region-specific translocations. Finally, SKY analysis revealed that radio-sensitivity of structurally rearranged chromosomes is dependent on radiation dose. These findings will advance our knowledge in 293 cell biology and will enrich the understanding of radiation biology studies.

摘要

人胚肾 293 细胞系(293 细胞)广泛应用于生物医学和药物研究。这些细胞表现出许多数量和结构染色体异常。然而,导致这些结构染色体重排的断裂点尚未得到全面描述。此外,尚不清楚是否具有结构重排的染色体对外界有毒剂(如电离辐射)更敏感。我们使用 G 带、光谱核型分析(SKY)和我们实验室设计或从商业供应商获得的基因座和区域特异性荧光原位杂交(FISH)探针来解决这一差距。我们的 G 带分析显示染色体数量从 66 到 71 不等,存在多种重排和部分缺失和添加。SKY 分析证实了 3 个一致的重排,其中 2 个是简单的,1 个是复杂的。多色 FISH 分析确定了一系列导致基因座和区域特异性易位的断裂点。最后,SKY 分析显示,结构重排染色体的放射敏感性取决于辐射剂量。这些发现将推进我们对 293 细胞生物学的认识,并丰富对放射生物学研究的理解。

相似文献

1
Identification of novel breakpoints for locus- and region-specific translocations in 293 cells by molecular cytogenetics before and after irradiation.采用分子细胞遗传学技术,在照射前后对 293 细胞中基因座和区域特异性易位的新型断点进行鉴定。
Sci Rep. 2019 Jul 22;9(1):10554. doi: 10.1038/s41598-019-47002-0.
2
Spectral karyotyping analysis of head and neck squamous cell carcinoma.头颈部鳞状细胞癌的光谱核型分析
Laryngoscope. 2001 Sep;111(9):1545-50. doi: 10.1097/00005537-200109000-00010.
3
Identification of recurrent chromosomal breakpoints in multiple myeloma with complex karyotypes by combined G-banding, spectral karyotyping, and fluorescence in situ hybridization analyses.通过联合G显带、光谱核型分析和荧光原位杂交分析鉴定具有复杂核型的多发性骨髓瘤中的复发性染色体断点。
Cancer Genet Cytogenet. 2006 Sep;169(2):143-9. doi: 10.1016/j.cancergencyto.2006.04.008.
4
Detection of Inter-chromosomal Stable Aberrations by Multiple Fluorescence In Situ Hybridization (mFISH) and Spectral Karyotyping (SKY) in Irradiated Mice.通过多重荧光原位杂交(mFISH)和光谱核型分析(SKY)检测辐照小鼠的染色体间稳定畸变
J Vis Exp. 2017 Jan 11(119):55162. doi: 10.3791/55162.
5
Multicolor Karyotyping and Fluorescence In Situ Hybridization-Banding (MCB/mBAND).多色核型分析与荧光原位杂交显带技术(MCB/mBAND)
Methods Mol Biol. 2017;1541:181-187. doi: 10.1007/978-1-4939-6703-2_16.
6
Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridization.慢性髓性白血病衍生细胞系K562的细胞遗传学:通过多色荧光原位杂交、比较基因组杂交和位点特异性荧光原位杂交进行核型分析
Cancer Genet Cytogenet. 2000 Apr 1;118(1):1-8. doi: 10.1016/s0165-4608(99)00169-7.
7
Multicolor banding technique, spectral color banding (SCAN): new development and applications.多色带技术,光谱色带(SCAN):新进展与应用
Cytogenet Genome Res. 2006;114(3-4):250-6. doi: 10.1159/000094209.
8
Multicolour spectral karyotyping for complex chromosomal rearrangements in repeated abortion or congenital anomalies.用于复发性流产或先天性异常中复杂染色体重排的多色光谱核型分析。
Prenat Diagn. 2001 Dec;21(13):1123-8. doi: 10.1002/pd.183.
9
Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping.采用光谱核型分析对膀胱癌细胞系BK-10进行分子细胞遗传学分析。
Genes Chromosomes Cancer. 1999 May;25(1):53-9. doi: 10.1002/(sici)1098-2264(199905)25:1<53::aid-gcc8>3.0.co;2-t.
10
Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints.染色体 6、10 和 11 之间的复杂重排,断裂点有多处缺失。
Am J Med Genet A. 2010 Sep;152A(9):2327-34. doi: 10.1002/ajmg.a.33581.

引用本文的文献

1
Precise correction of G6PD Viangchan mutation in iPSCs by prime editing strategy.通过碱基编辑策略对诱导多能干细胞中的G6PD万象突变进行精确校正。
Sci Rep. 2025 Aug 18;15(1):30192. doi: 10.1038/s41598-025-15463-1.
2
Precision multiplexed base editing in human cells using Cas12a-derived base editors.使用源自Cas12a的碱基编辑器在人类细胞中进行精确多重碱基编辑。
Nat Commun. 2025 May 31;16(1):5061. doi: 10.1038/s41467-025-59653-x.
3
G-Banding and Molecular Cytogenetics Detect Novel Translocations and Cryptic Aberrations in Human Immortal Endothelial Cells.

本文引用的文献

1
Fluorescence In Situ Hybridization (FISH) in Multiple Myeloma.多发性骨髓瘤中的荧光原位杂交(FISH)
Methods Mol Biol. 2018;1792:55-69. doi: 10.1007/978-1-4939-7865-6_5.
2
Human Embryonic Kidney 293 Cells: A Vehicle for Biopharmaceutical Manufacturing, Structural Biology, and Electrophysiology.人胚肾293细胞:生物制药生产、结构生物学和电生理学的载体。
Cells Tissues Organs. 2018;205(1):1-8. doi: 10.1159/000485501. Epub 2018 Feb 1.
3
Scalable Lentiviral Vector Production Using Stable HEK293SF Producer Cell Lines.利用稳定的HEK293SF生产细胞系进行可扩展的慢病毒载体生产
G 带和分子细胞遗传学检测人永生化内皮细胞中的新型易位和隐匿性畸变。
Int J Mol Sci. 2024 Jul 20;25(14):7941. doi: 10.3390/ijms25147941.
4
A Knockout of Poly(ADP-Ribose) Polymerase 1 in a Human Cell Line: An Influence on Base Excision Repair Reactions in Cellular Extracts.一个人源细胞系中聚(ADP-核糖)聚合酶 1 的敲除:对细胞抽提物中碱基切除修复反应的影响。
Cells. 2024 Feb 6;13(4):302. doi: 10.3390/cells13040302.
5
Genotyping MUltiplexed-Sequencing of CRISPR-Localized Editing (GMUSCLE): An Experimental and Computational Approach for Analyzing CRISPR-Edited Cells.基于 CRISPR 定位编辑的基因分型多重测序(GMUSCLE):分析 CRISPR 编辑细胞的实验和计算方法。
CRISPR J. 2023 Oct;6(5):462-472. doi: 10.1089/crispr.2023.0021.
6
CRISPR prime editing for unconstrained correction of oncogenic KRAS variants.CRISPR 先导编辑技术用于无约束纠正致癌性 KRAS 变异。
Commun Biol. 2023 Jun 30;6(1):681. doi: 10.1038/s42003-023-05052-1.
7
Targeted assembly of ectopic kinetochores to induce chromosome-specific segmental aneuploidies.靶向组装异位着丝粒以诱导染色体特异性片段非整倍体。
EMBO J. 2023 May 15;42(10):e111587. doi: 10.15252/embj.2022111587. Epub 2023 Apr 17.
8
Evaluating the effects of low-dose simulated galactic cosmic rays on murine hippocampal-dependent cognitive performance.评估低剂量模拟银河系宇宙射线对小鼠海马体依赖性认知能力的影响。
Front Neurosci. 2022 Dec 6;16:908632. doi: 10.3389/fnins.2022.908632. eCollection 2022.
9
Cytogenetic and epigenetic aberrations in peripheral lymphocytes of northwest Arkansas Marshallese.阿肯色州西北马歇尔群岛人外周血淋巴细胞的细胞遗传学和表观遗传学异常。
Int J Radiat Biol. 2023;99(4):644-655. doi: 10.1080/09553002.2022.2110319. Epub 2022 Aug 15.
10
Molecular Cytogenetics Reveals Mosaicism in Human Umbilical Vein Endothelial Cells.分子细胞遗传学揭示了人类脐静脉内皮细胞中的嵌合体现象。
Genes (Basel). 2022 Jun 3;13(6):1012. doi: 10.3390/genes13061012.
Hum Gene Ther Methods. 2017 Dec;28(6):330-339. doi: 10.1089/hgtb.2017.086. Epub 2017 Nov 21.
4
Role of chromosomal instability in cancer progression.染色体不稳定在癌症进展中的作用。
Endocr Relat Cancer. 2017 Sep;24(9):T23-T31. doi: 10.1530/ERC-17-0187. Epub 2017 Jul 10.
5
Detection of Inter-chromosomal Stable Aberrations by Multiple Fluorescence In Situ Hybridization (mFISH) and Spectral Karyotyping (SKY) in Irradiated Mice.通过多重荧光原位杂交(mFISH)和光谱核型分析(SKY)检测辐照小鼠的染色体间稳定畸变
J Vis Exp. 2017 Jan 11(119):55162. doi: 10.3791/55162.
6
Analysis of the Ambient Particulate Matter-induced Chromosomal Aberrations Using an In Vitro System.使用体外系统分析环境颗粒物诱导的染色体畸变
J Vis Exp. 2016 Dec 21(118):54969. doi: 10.3791/54969.
7
Rapid high-throughput cloning and stable expression of antibodies in HEK293 cells.抗体在HEK293细胞中的快速高通量克隆与稳定表达。
J Immunol Methods. 2016 Dec;439:50-58. doi: 10.1016/j.jim.2016.09.007. Epub 2016 Sep 24.
8
Immunoprecipitation and mass spectrometry defines an extensive RBM45 protein-protein interaction network.免疫沉淀和质谱分析确定了一个广泛的RBM45蛋白质-蛋白质相互作用网络。
Brain Res. 2016 Sep 15;1647:79-93. doi: 10.1016/j.brainres.2016.02.047. Epub 2016 Mar 12.
9
Human cell lines for biopharmaceutical manufacturing: history, status, and future perspectives.用于生物制药生产的人类细胞系:历史、现状与未来展望。
Crit Rev Biotechnol. 2016 Dec;36(6):1110-1122. doi: 10.3109/07388551.2015.1084266. Epub 2015 Sep 18.
10
HEK293 in cell biology and cancer research: phenotype, karyotype, tumorigenicity, and stress-induced genome-phenotype evolution.细胞生物学和癌症研究中的HEK293:表型、核型、致瘤性以及应激诱导的基因组-表型进化
Gene. 2015 Sep 15;569(2):182-90. doi: 10.1016/j.gene.2015.05.065. Epub 2015 May 27.