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用碱性品红对人类染色体进行前中期显带

Prometaphase banding of human chromosomes with basic fuchsin.

作者信息

Scheres J M, Merkx G F, Hustinx T W

出版信息

Hum Genet. 1982;61(1):8-11. doi: 10.1007/BF00291322.

DOI:10.1007/BF00291322
PMID:7129436
Abstract

A technique is described for the production of detailed and richly contrasting G-band patterns in human prometaphase chromosomes with the aid of the triphenylmethane dye basic fuchsin. The usefulness of this method is illustrated by its application for the precise analysis of two chromosome 11 rearrangements. It is also demonstrated that high-resolution banding with basic fuchsin can reveal bands not present in the international standard idiogram of human prophase chromosomes (ISCN 1981). The technique described can also be used for easy recognition of the late replicating X chromosome, which stains darker than its early replicating homologue. A preliminary analysis of the late replicating X chromosomes in a 49,XXXXY individual suggests that the three supernumerary X chromosomes do not necessarily replicate synchronously.

摘要

本文描述了一种借助三苯甲烷染料碱性品红在人类早中期染色体上产生详细且对比度丰富的G带模式的技术。通过将该方法应用于两条11号染色体重排的精确分析,说明了此方法的实用性。还证明了用碱性品红进行高分辨率显带可揭示人类前期染色体国际标准核型图(ISCN 1981)中不存在的带。所描述的技术还可用于轻松识别晚复制的X染色体,其染色比早复制的同源染色体更深。对一名49,XXXXY个体中晚复制X染色体的初步分析表明,三条额外的X染色体不一定同步复制。

相似文献

1
Prometaphase banding of human chromosomes with basic fuchsin.用碱性品红对人类染色体进行前中期显带
Hum Genet. 1982;61(1):8-11. doi: 10.1007/BF00291322.
2
R-banding of human chromosomes by heat denaturation and Giemsa staining after amethopterin-synchronization.氨甲蝶呤同步化后经热变性和吉姆萨染色对人类染色体进行R显带。
Can J Genet Cytol. 1983 Jun;25(3):261-9. doi: 10.1139/g83-041.
3
The characterization of high-resolution G-banded chromosomes of man.人类高分辨率G带染色体的特征分析。
Chromosoma. 1978 Aug 14;67(4):293-307. doi: 10.1007/BF00285963.
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Banding of human chromosomes with basic fuchsin.用碱性品红对人类染色体进行显带处理。
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G-banding patterns of high-resolution human chromosomes 6--22, X, and Y.高分辨率人类染色体6 - 22、X和Y的G带模式。
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A high-resolution G-banding idiogram of Rattus norvegicus chromosomes.褐家鼠染色体的高分辨率G带核型模式图。
Cytobios. 1990;62(250-251):153-60.
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High-resolution idiogram of Giemsa R-banded human prophase chromosomes.吉姆萨R带人类早前期染色体的高分辨率染色体模式图。
Can J Genet Cytol. 1983 Dec;25(6):642-50. doi: 10.1139/g83-095.
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Analysis of high-resolution R-bands, obtained by heat-denaturation and Giemsa staining, on human prophase chromosomes.对通过热变性和吉姆萨染色获得的人类前期染色体高分辨率R带进行分析。
Can J Genet Cytol. 1985 Feb;27(1):83-91. doi: 10.1139/g85-014.
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The use of subchromosome-length unique band sequences in the analysis of prophase chromosomes.亚染色体长度独特带序列在前期染色体分析中的应用。
Am J Hum Genet. 1988 Dec;43(6):934-47.
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Light and scanning electron microscopy of the same human metaphase chromosomes.同一人类中期染色体的光学显微镜和扫描电子显微镜观察
J Cell Sci. 1985 Aug;77:143-53. doi: 10.1242/jcs.77.1.143.

引用本文的文献

1
49,XXXXY: a distinct phenotype. Three new cases and review.49,XXXXY:一种独特的表型。三例新病例及文献复习
J Med Genet. 1998 May;35(5):420-4. doi: 10.1136/jmg.35.5.420.
2
Molecular study of chromosome 15 in 22 patients with Angelman syndrome.对22例天使综合征患者的15号染色体进行分子研究。
Hum Genet. 1993 Jan;90(5):489-95. doi: 10.1007/BF00217446.
3
Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.13号染色体长臂缺失与瓦登伯格综合征:13q上存在参与神经嵴功能基因的进一步证据

本文引用的文献

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Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.15号染色体缺失是普拉德-威利综合征的病因。
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The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24.人类甲状腺球蛋白基因:一种多态性标记,定位于8号染色体q24带,在C-MYC远端。
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Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent.由于父母一方发生复杂的五断点染色体重排,导致一名活产婴儿出现5q部分三体和12p单体。
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Mid-prophase human chromosomes. The attainment of 2000 bands.中期人类染色体。达到2000条带纹。
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5
Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.在几个不相关的家族中出现特定部位的相互易位,即t(11;22) (q23;q11),伴有3:1减数分裂分离。
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The 11q;22q translocation: a European collaborative analysis of 43 cases.11号染色体与22号染色体易位:43例病例的欧洲协作分析
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7
Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.伴有11p13 - 14.1缺失的无虹膜 - 威尔姆斯瘤综合征的家族性发生情况。
J Pediatr. 1980 Jun;96(6):1027-30. doi: 10.1016/s0022-3476(80)80630-5.
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High resolution of human chromosomes.人类染色体的高分辨率。
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"Reverse" differential staining of sister chromatids.姐妹染色单体的“反向”差异染色
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R- and CT-banding of human chromosomes with basic fuchsin.用碱性品红对人类染色体进行R带和CT带分析。
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