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利用体细胞杂种中的亚染色体片段对人类19号染色体上的遗传标记进行定位。

Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids.

作者信息

Brook J D, Shaw D J, Thomas N S, Meredith A L, Cowell J, Harper P S

出版信息

Cytogenet Cell Genet. 1986;41(1):30-7. doi: 10.1159/000132192.

DOI:10.1159/000132192
PMID:3455910
Abstract

A series of mouse-human somatic cell hybrid lines (WILF) were derived from a hybrid that was originally thought to have chromosome 19 as its only human chromosome. In situ hybridization has been used to assess the amount of human material present in the different lines. All appear to contain different numbers of human chromosome fragments. A series of X-chromosome-specific DNA sequences hybridized against DNA from the lines revealed that material from the X long arm is present in several cases. Chromosome 19-specific DNA sequences used in a similar way show that fragmentation of this this chromosome has occurred with subsequent segregation of the fragments in different lines. The localization of these markers to various regions of chromosome 19, and their relation to the fragments observed in the WILF lines, is discussed.

摘要

一系列小鼠 - 人类体细胞杂交系(WILF)源自一个最初被认为仅含人类19号染色体的杂交细胞。原位杂交已用于评估不同细胞系中人类物质的含量。所有细胞系似乎都含有不同数量的人类染色体片段。一系列X染色体特异性DNA序列与这些细胞系的DNA杂交显示,在一些情况下存在来自X染色体长臂的物质。以类似方式使用的19号染色体特异性DNA序列表明,这条染色体发生了片段化,随后片段在不同细胞系中分离。本文讨论了这些标记物在19号染色体各个区域的定位,以及它们与在WILF细胞系中观察到的片段的关系。

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Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids.利用体细胞杂种中的亚染色体片段对人类19号染色体上的遗传标记进行定位。
Cytogenet Cell Genet. 1986;41(1):30-7. doi: 10.1159/000132192.
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引用本文的文献

1
Regional assignment of the gene for diphtheria toxin sensitivity using subchromosomal fragments in microcell hybrids.利用微细胞杂种中的亚染色体片段对白喉毒素敏感性基因进行区域定位。
Chromosoma. 1987;96(1):26-32. doi: 10.1007/BF00285879.
2
Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair.位于15号和19号染色体上的人类肌酸激酶基因,以及肌肉型基因与载脂蛋白C2基因和切除修复基因的邻近关系。
Am J Hum Genet. 1988 Aug;43(2):144-51.
3
A polymorphic DNA clone which maps to 19p13.2----19q12 (D19S27).
一个定位于19p13.2至19q12(D19S27)的多态性DNA克隆。
Nucleic Acids Res. 1988 Aug 11;16(15):7751. doi: 10.1093/nar/16.15.7751.
4
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.19号染色体上七个限制性片段长度多态性(RFLP)与强直性肌营养不良的区域定位及连锁关系
Hum Genet. 1986 Nov;74(3):262-6. doi: 10.1007/BF00282545.
5
Confirmation and refinement of the localisation of the c-MEL locus on chromosome 19 by physical and genetic mapping.
Hum Genet. 1989 Mar;81(4):382-4. doi: 10.1007/BF00283697.
6
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.强直性肌营养不良基因座与一种新的多态性DNA标记之间连锁不平衡的检测。
Am J Hum Genet. 1991 Jul;49(1):68-75.
7
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.强直性肌营养不良基因座定位于19q13.2 - 19q13.3及其与19q上12个多态性基因座的关系。
Hum Genet. 1991 May;87(1):73-80. doi: 10.1007/BF01213096.
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The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments.19号染色体长臂的物理图谱:一些新的定位、确认和重新评估。
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A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.
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