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本文引用的文献

1
Microscopy and image analysis.显微镜检查与图像分析。
Curr Protoc Hum Genet. 2005 Aug;Chapter 4:Unit 4.4. doi: 10.1002/0471142905.hg0404s46.
2
Multiplex-fluorescence in situ hybridization for chromosome karyotyping.用于染色体核型分析的多重荧光原位杂交技术。
Nat Protoc. 2006;1(3):1172-84. doi: 10.1038/nprot.2006.160.
3
Cross-species chromosome painting.跨物种染色体描绘
Nat Protoc. 2006;1(2):783-90. doi: 10.1038/nprot.2006.91.
4
Spectral karyotyping of human, mouse, rat and ape chromosomes--applications for genetic diagnostics and research.人类、小鼠、大鼠和猿类染色体的光谱核型分析——在基因诊断和研究中的应用
Cytogenet Genome Res. 2006;114(3-4):199-221. doi: 10.1159/000094203.
5
The interactive online SKY/M-FISH & CGH database and the Entrez cancer chromosomes search database: linkage of chromosomal aberrations with the genome sequence.交互式在线SKY/M-FISH与CGH数据库及Entrez癌症染色体搜索数据库:染色体畸变与基因组序列的关联
Genes Chromosomes Cancer. 2005 Sep;44(1):52-64. doi: 10.1002/gcc.20224.
6
Pediatric pancreatoblastoma: histopathologic and cytogenetic characterization of tumor and derived cell line.小儿胰腺母细胞瘤:肿瘤及其衍生细胞系的组织病理学和细胞遗传学特征
Cancer Genet Cytogenet. 2005 Mar;157(2):109-17. doi: 10.1016/j.cancergencyto.2004.05.017.
7
Prenatal diagnosis of minute supernumerary marker chromosomes.微小额外标记染色体的产前诊断
Gynecol Obstet Invest. 2005;60(1):27-38. doi: 10.1159/000083482. Epub 2005 Jan 24.
8
Multicolor spectral karyotyping of rat chromosomes.大鼠染色体的多色光谱核型分析。
Cytogenet Genome Res. 2003;103(1-2):163-8. doi: 10.1159/000076306.
9
The Septin 9 (MSF) gene is amplified and overexpressed in mouse mammary gland adenocarcinomas and human breast cancer cell lines.Sept9(MSF)基因在小鼠乳腺腺癌和人乳腺癌细胞系中被扩增并过度表达。
Cancer Res. 2003 May 1;63(9):2179-87.
10
Mammary tumors in mice conditionally mutant for Brca1 exhibit gross genomic instability and centrosome amplification yet display a recurring distribution of genomic imbalances that is similar to human breast cancer.在Brca1条件性突变的小鼠中,乳腺肿瘤表现出明显的基因组不稳定性和中心体扩增,但仍呈现出与人类乳腺癌相似的基因组失衡复发分布。
Oncogene. 2002 Aug 1;21(33):5097-107. doi: 10.1038/sj.onc.1205636.

人类和小鼠染色体的光谱核型分析。

Spectral karyotyping analysis of human and mouse chromosomes.

作者信息

Padilla-Nash Hesed M, Barenboim-Stapleton Linda, Difilippantonio Michael J, Ried Thomas

机构信息

Genetics Branch, Center for Cancer Research, National Cancer Institute, US National Institutes of Health, 50 South Drive-MSC 8010, Bethesda, Maryland 20892, USA.

出版信息

Nat Protoc. 2006;1(6):3129-42. doi: 10.1038/nprot.2006.358.

DOI:10.1038/nprot.2006.358
PMID:17406576
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4772431/
Abstract

Classical banding methods provide basic information about the identities and structures of chromosomes on the basis of their unique banding patterns. Spectral karyotyping (SKY), and the related multiplex fluorescence in situ hybridization (M-FISH), are chromosome-specific multicolor FISH techniques that augment cytogenetic evaluations of malignant disease by providing additional information and improved characterization of aberrant chromosomes that contain DNA sequences not identifiable using conventional banding methods. SKY is based on cohybridization of combinatorially labeled chromosome-painting probes with unique fluorochrome signatures onto human or mouse metaphase chromosome preparations. Image acquisition and analysis use a specialized imaging system, combining Sagnac interferometer and CCD camera images to reconstruct spectral information at each pixel. Here we present a protocol for SKY analysis using commercially available SkyPaint probes, including procedures for metaphase chromosome preparation, slide pretreatment and probe hybridization and detection. SKY analysis requires approximately 6 d.

摘要

经典的显带方法基于染色体独特的带型模式提供有关其身份和结构的基本信息。光谱核型分析(SKY)以及相关的多重荧光原位杂交(M-FISH)是针对染色体的多色FISH技术,通过提供额外信息并改进对包含使用传统显带方法无法识别的DNA序列的异常染色体的表征,增强了对恶性疾病的细胞遗传学评估。SKY基于组合标记的染色体涂染探针与独特荧光染料标记物共同杂交到人类或小鼠中期染色体标本上。图像采集和分析使用专门的成像系统,结合萨尼亚克干涉仪和电荷耦合器件相机图像来重建每个像素处的光谱信息。在此,我们介绍一种使用市售SkyPaint探针进行SKY分析的方案,包括中期染色体标本制备及玻片预处理、探针杂交和检测的步骤。SKY分析大约需要6天时间。