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检测21号染色体特异性α-卫星DNA序列的新方法。

Novel methodology for the detection of chromosome 21-specific alpha-satellite DNA sequences.

作者信息

Maratou K, Siddique Y, Kessling A M, Davies G E

机构信息

Department of Medical and Community Genetics, Imperial College of Science, Technology and Medicine, London, HA1 3UJ, United Kingdom.

出版信息

Genomics. 1999 May 1;57(3):429-32. doi: 10.1006/geno.1999.5786.

Abstract

We present a novel method, based on the hybridization of allele-specific oligonucleotide probes, that allows the specific detection of chromosome 21 alpha-satellite sequences. Absence of informative polymorphic markers from the centromeric region of chromosome 21 has constituted one of the difficulties in studying the centromere of this chromosome. The alpha-satellite subfamilies from chromosomes 21 and 13 are almost identical in sequence and thus cannot be distinguished using conventional hybridization techniques. Analysis using nuclear families showed that the centromeric polymorphism, detected using our specific probe and pulsed-field gel restriction analysis, segregates in a Mendelian fashion and exhibits a high degree of polymorphism among unrelated individuals. The alphoid DNA of chromosome 21 is highly polymorphic, useful not only as a definitive anchor for the genetic map, but also for studies of chromosome 21 nondisjunction, including the unequivocal assignment of meiotic origin.

摘要

我们提出了一种基于等位基因特异性寡核苷酸探针杂交的新方法,该方法能够特异性检测21号染色体的α-卫星序列。21号染色体着丝粒区域缺乏信息丰富的多态性标记,这一直是研究该染色体着丝粒的困难之一。21号和13号染色体的α-卫星亚家族在序列上几乎相同,因此无法使用传统杂交技术进行区分。利用核心家庭进行的分析表明,使用我们的特异性探针和脉冲场凝胶限制性分析检测到的着丝粒多态性,以孟德尔方式分离,并且在无关个体中表现出高度多态性。21号染色体的α-卫星DNA具有高度多态性,不仅可作为遗传图谱的明确锚定物,还可用于研究21号染色体不分离,包括明确减数分裂起源的归属。

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