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39个随机分离的Y染色体DNA片段的缺失图谱分析。

Deletion mapping of 39 random isolated Y-chromosome DNA fragments.

作者信息

Oosthuizen C J, Herbert J S, Vermaak L K, Brusnicky J, Fricke J, du Plessis L, Retief A E

机构信息

Department of Human Genetics, Tygerberg Hospital, Republic of South Africa.

出版信息

Hum Genet. 1990 Jul;85(2):205-10. doi: 10.1007/BF00193197.

DOI:10.1007/BF00193197
PMID:2370050
Abstract

Thirty-nine recombinants isolated from a Y chromosome-specific library were deletion mapped. Seven deletion intervals were defined by hybridization of probes to DNA of eight individuals with aberrant Y chromosomes. Extreme cytogenetic limits of the deletion intervals were determined by in situ hybridization of one probe per deletion interval. Five intervals, with a total of twenty-five probes, were allocated to the long-arm euchromatic region. The probes described will be useful for characterization of aberrant Y chromosomes, in searching for expressed sequences on the Y chromosome, and for further study of the evolutionary relationship between the Y chromosome and other chromosomes.

摘要

从一个Y染色体特异性文库中分离出的39个重组体进行了缺失定位。通过将探针与8个具有异常Y染色体个体的DNA杂交,确定了7个缺失区间。每个缺失区间通过一个探针的原位杂交确定了缺失区间的极端细胞遗传学界限。5个区间,共25个探针,被分配到长臂常染色质区域。所描述的探针将有助于异常Y染色体的特征分析、在Y染色体上寻找表达序列以及进一步研究Y染色体与其他染色体之间的进化关系。

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本文引用的文献

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KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.性腺发育不全中的核型-表型相关性及其对畸形发病机制的影响
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Characterisation of a human Y chromosome repeated sequence and related sequences in higher primates.
人类Y染色体重复序列及高等灵长类相关序列的特征分析
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A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.一个来自人类X染色体短臂的DNA片段,它能检测到Y染色体长臂上的一个部分同源序列。
Nucleic Acids Res. 1984 May 25;12(10):4097-109. doi: 10.1093/nar/12.10.4097.
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Extensive sequence homologies between Y and other human chromosomes.Y染色体与其他人类染色体之间存在广泛的序列同源性。
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Actin-like sequences are present on human X and Y chromosomes.肌动蛋白样序列存在于人类X和Y染色体上。
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Human XX males with Y single-copy DNA fragments.携带Y单拷贝DNA片段的人类XX男性。
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Genetic evidence of X-Y interchange in a human XX male.一名人类XX男性中X-Y染色体互换的遗传学证据。
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Human satellite I sequences include a male specific 2.47 kb tandemly repeated unit containing one Alu family member per repeat.人类卫星I序列包括一个男性特异性的2.47 kb串联重复单元,每个重复单元包含一个Alu家族成员。
Nucleic Acids Res. 1984 Mar 26;12(6):2887-900. doi: 10.1093/nar/12.6.2887.