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用于快速筛选α卫星13号和21号染色体特异性黏粒克隆特异性的双色原位杂交。

Double color in situ hybridization of alpha-satellite chromosome 13, 21 specific cosmid clones for a rapid screening of their specificity.

作者信息

Soloviev I V, Vorsanova S G, Malet P, Zerova T E, Buzhievskaya T I

机构信息

National Research Center of Mental Health, RAMS, Moscow.

出版信息

Tsitol Genet. 1998 Jul-Aug;32(4):60-4.

PMID:9813889
Abstract

Double color in situ hybridization was used to determine the specificity of cloned alpha-satellite cosmid DNA sequences belonging to satellite DNA sequences shared by chromosomes 13 and 21. It was determined that cosmid clone cos56D8 is more specific to chromosome 13, cosmid clone cos37E is more specific to chromosome 21 and cosmid clones cosA5130 is specific to both chromosomes 13 and 21. These new cosmid probes could bw useful in the molecular-cytogenetic analysis of trisomic cells at Patau or Down syndromes as well as in analysis of marker chromosomes originated from the chromosomes 13 and 21.

摘要

采用双色原位杂交技术来确定属于13号和21号染色体共有的卫星DNA序列的克隆α-卫星黏粒DNA序列的特异性。已确定黏粒克隆cos56D8对13号染色体更具特异性,黏粒克隆cos37E对21号染色体更具特异性,而黏粒克隆cosA5130对13号和21号染色体均具有特异性。这些新的黏粒探针可用于帕陶氏综合征或唐氏综合征三体细胞的分子细胞遗传学分析,以及源自13号和21号染色体的标记染色体的分析。

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Double color in situ hybridization of alpha-satellite chromosome 13, 21 specific cosmid clones for a rapid screening of their specificity.用于快速筛选α卫星13号和21号染色体特异性黏粒克隆特异性的双色原位杂交。
Tsitol Genet. 1998 Jul-Aug;32(4):60-4.
2
[Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization].[使用荧光原位杂交技术对13号、21号和22号染色体特异性黏粒文库中的α卫星DNA进行研究]
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Padlock probes reveal single-nucleotide differences, parent of origin and in situ distribution of centromeric sequences in human chromosomes 13 and 21.锁式探针揭示了人类13号和21号染色体着丝粒序列的单核苷酸差异、起源亲本及原位分布。
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A degenerate alpha satellite probe, detecting a centromeric deletion on chromosome 21 in an apparently normal human male, shows limitations of the use of satellite DNA probes for interphase ploidy analysis.一个退化的α卫星探针,在一名外表正常的男性中检测到21号染色体上的着丝粒缺失,这显示了卫星DNA探针在间期倍性分析中的应用局限性。
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[Human alpha-satellite DNA specific to chromosomes 13 and 21: use for the analysis of polymorphism of acrocentric chromosomes and the origin of the additional chromosome 21 in Down's syndrome].[人类13号和21号染色体特异性α卫星DNA:用于近端着丝粒染色体多态性分析及唐氏综合征中额外21号染色体的起源研究]
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Isolation and characterization of DNA probes for human chromosome 21.人类21号染色体DNA探针的分离与特性分析
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A fluorescence in situ hybridization map of human chromosome 21 consisting of 30 genetic and physical markers on the chromosome: localization of 137 additional YAC and cosmid clones with respect to this map.一张人类21号染色体的荧光原位杂交图谱,该图谱由染色体上的30个遗传和物理标记组成:137个额外的酵母人工染色体(YAC)和黏粒克隆相对于此图谱的定位。
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