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Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool.

作者信息

Deng H X, Yoshiura K, Dirks R W, Harada N, Hirota T, Tsukamoto K, Jinno Y, Niikawa N

机构信息

Department of Human Genetics, Nagasaki University School of Medicine, Japan.

出版信息

Hum Genet. 1992 Apr;89(1):13-7. doi: 10.1007/BF00207034.

DOI:10.1007/BF00207034
PMID:1577461
Abstract

We describe a chromosome-band-specific painting method that involves (1) microdissection of the chromosome, chromosomal region or band, (2) amplification of a variety of chromosome/region/band-specific DNA fragments with the polymerase chain reaction (PCR), and (3) chromosome in situ suppression hybridization (CISS) with the direct use of the PCR products as a probe pool. With this method, it was possible 1) to paint an entire X or Y chromosome, a distal one-fourth of 2q, and only a band at 8q24.1, 2) to identify the origin of a minute marker chromosome in a mentally retarded patient, 3) to detect an X;Y translocation in another patient, and 4) to identify one human chromosome 2 in a human-mouse hybrid cell line. This method allows us to identify not only structural chromosome abnormalities at the band level, but also the origin of cytogenetically unidentifiable marker chromosomes. It will also be useful in studies of evolutionary cytogenetics.

摘要

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1
Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool.
Hum Genet. 1992 Apr;89(1):13-7. doi: 10.1007/BF00207034.
2
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4
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本文引用的文献

1
Novel non-isotopic in situ hybridization technique detects small (1 Kb) unique sequences in routinely G-banded human chromosomes: fine mapping of N-myc and beta-NGF genes.新型非同位素原位杂交技术可检测常规G显带人类染色体中的小(1千碱基)独特序列:N-myc和β-神经生长因子基因的精细定位
Nucleic Acids Res. 1987 Jun 25;15(12):4761-70. doi: 10.1093/nar/15.12.4761.
2
Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes.使用染色体特异性文库探针通过原位杂交检测中期和间期肿瘤细胞中的染色体畸变。
Hum Genet. 1988 Nov;80(3):235-46. doi: 10.1007/BF01790091.
3
通过激光显微切割和接头-衔接子PCR从单条染色体生成染色体涂染探针。
Chromosome Res. 2004;12(4):337-43. doi: 10.1023/B:CHRO.0000034132.77192.5f.
4
Chromosome paints from single copies of chromosomes.来自单条染色体拷贝的染色体涂染探针。
Chromosome Res. 2004;12(2):143-51. doi: 10.1023/b:chro.0000013167.12527.f0.
5
Reverse painting highlights the origin of chromosome aberrations.反向绘画突出了染色体畸变的起源。
Chromosome Res. 2004;12(1):25-33. doi: 10.1023/b:chro.0000009277.42798.9a.
6
Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation.通过比较基因组杂交鉴定出的镶嵌型额外环状19号染色体。
J Med Genet. 1998 Oct;35(10):836-40. doi: 10.1136/jmg.35.10.836.
7
A simple and efficient method for microdissection and microFISH.一种用于显微切割和显微荧光原位杂交的简单高效方法。
J Med Genet. 1998 Apr;35(4):265-8. doi: 10.1136/jmg.35.4.265.
8
A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q.一例与3q染色体新生三体相关的单侧睑裂狭小综合征和智力障碍的罕见病例。
J Med Genet. 1997 Sep;34(9):772-6. doi: 10.1136/jmg.34.9.772.
9
Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH.通过显微切割和荧光原位杂交技术揭示复杂染色体重排中的五个断点
J Med Genet. 1996 Jul;33(7):562-6. doi: 10.1136/jmg.33.7.562.
10
Generation of chromosome fragment specific bovine DNA sequences by microdissection and DOP-PCR.通过显微切割和DOP-PCR技术生成染色体片段特异性牛DNA序列
Mamm Genome. 1996 Apr;7(4):291-6. doi: 10.1007/s003359900085.
Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries.
利用重组DNA文库通过原位抑制杂交技术描绘中期和间期细胞中的单个人类染色体。
Hum Genet. 1988 Nov;80(3):224-34. doi: 10.1007/BF01790090.
4
Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes.使用染色体特异性重复DNA探针检测人原发性乳腺肿瘤间期细胞核中的染色体非整倍性。
Cancer Res. 1988 Oct 15;48(20):5825-30.
5
Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.使用人类染色体特异性文库进行荧光原位杂交:检测21三体和4号染色体易位
Proc Natl Acad Sci U S A. 1988 Dec;85(23):9138-42. doi: 10.1073/pnas.85.23.9138.
6
Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification.通过对带型染色体进行显微切割和酶促扩增来克隆人类基因组的特定区域。
Nature. 1989 Mar 23;338(6213):348-50. doi: 10.1038/338348a0.
7
Detection of chromosome aberrations in interphase tumor nuclei by nonradioactive in situ hybridization.通过非放射性原位杂交检测间期肿瘤细胞核中的染色体畸变。
Cancer Genet Cytogenet. 1989 Oct 1;42(1):87-98. doi: 10.1016/0165-4608(89)90011-3.
8
Construction of mouse A9 clones containing a single human chromosome tagged with neomycin-resistance gene via microcell fusion.通过微细胞融合构建含有一条用新霉素抗性基因标记的单个人类染色体的小鼠A9克隆。
Jpn J Cancer Res. 1989 May;80(5):413-8. doi: 10.1111/j.1349-7006.1989.tb02329.x.
9
Three-color fluorescence in situ hybridization for the simultaneous detection of multiple nucleic acid sequences.用于同时检测多个核酸序列的三色荧光原位杂交技术。
Cytometry. 1989 Jan;10(1):20-7. doi: 10.1002/cyto.990100105.
10
Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics.人类性染色体和常染色体的染色体原位抑制杂交及其在临床细胞遗传学中的应用。
Hum Genet. 1990 Jul;85(2):145-50. doi: 10.1007/BF00193186.