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人类D1S80基因座的微变异

Microvariation at the human D1S80 locus.

作者信息

Duncan G T, Balamurugan K, Budowle B, Smerick J, Tracey M L

机构信息

Department of Biology, Florida International University, Miami 33199, USA.

出版信息

Int J Legal Med. 1997;110(3):150-4. doi: 10.1007/s004140050054.

Abstract

The minisatellite locus D1S80, (location: 1p35-p36) GenBank sequence accession # D28507), is a variable number of tandem repeat (VNTR) locus with a 16 base pair repeat size. The sequence of the predominant core repeat region and variants of the D1S80 locus were determined to ascertain whether sequence variation or size variation is the cause of altered migration of some D1S80 alleles. A total of 23 alleles from 14 individuals, previously typed based on the number of repeats (i.e. nominal alleles) for the D1S80 locus, were selected for sequence analysis. The individuals were from African American, Caucasian, and Hispanic databases. From these, 18 different repeat unit sequences were observed and arbitrarily designated A-R. Structural relationships between the alleles became more apparent when the arrays of repeat units were divided into common motifs or super-repeat domains. Six motifs ranging from 3 to 9 repeat units were identified. Several of the alleles included repeat arrays which were too diverse to predict an evolutionary relationship, however, there are two general repeat motif arrays and each has some relationship with either the 18 or the 24 repeat allele. The D1S80 allelic polymorphism is primarily due to variation in the number of repeat units and to sequence variation among repeats, however, it can not be ruled out that some rare alleles may be due to insertions or deletions.

摘要

小卫星基因座D1S80(位置:1p35 - p36;GenBank序列登录号:D28507)是一个可变串联重复序列(VNTR)基因座,重复序列大小为16个碱基对。确定了D1S80基因座主要核心重复区域的序列及其变体,以确定序列变异或大小变异是否是某些D1S80等位基因迁移改变的原因。从之前根据D1S80基因座重复次数(即名义等位基因)分型的14个人中总共选择了23个等位基因进行序列分析。这些个体来自非裔美国人、白种人和西班牙裔数据库。从中观察到18种不同的重复单元序列,并随意命名为A - R。当将重复单元阵列划分为共同基序或超级重复域时,等位基因之间的结构关系变得更加明显。鉴定出了6种由3至9个重复单元组成的基序。然而,其中一些等位基因包含的重复阵列过于多样,无法预测进化关系,不过,存在两种一般的重复基序阵列,且每种都与18或24个重复等位基因存在某种关系。D1S80等位基因多态性主要是由于重复单元数量的变异以及重复序列之间的序列变异,但是,不能排除某些罕见等位基因可能是由于插入或缺失造成的。

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