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来自人类12号染色体的21个多态性标记,用于整合遗传图谱和物理图谱。

Twenty-one polymorphic markers from human chromosome 12 for integration of genetic and physical maps.

作者信息

LeBlanc-Straceski J M, Montgomery K T, Kissel H, Murtaugh L, Tsai P, Ward D C, Krauter K S, Kucherlapati R

机构信息

Department of Molecular Genetics, Albert Einstein College of Medicine, Bronx, New York 10461.

出版信息

Genomics. 1994 Jan 15;19(2):341-9. doi: 10.1006/geno.1994.1067.

Abstract

Twenty-one physically mapped, polymorphic markers have been developed from a chromosome 12-specific cosmid library. The markers consist of CA repeat-containing sequence-tagged sites (STSs) derived from cosmid clones mapped by fluorescence in situ hybridization (FISH). Three methods for determining the sequence flanking CA microsatellites were used, including one using degenerate primer sets for direct sequence analysis. Oligonucleotide primer pairs suitable for use in polymerase chain reaction (PCR) were selected from the sequences flanking the CA microsatellite and were tested for their ability to generate unique PCR products. The informativeness of these STSs as genetic markers was determined by typing 10 unrelated individuals who are part of the Centre d'Etude du Polymorphisme Humaine (EPH) pedigrees. Eleven of the 21 FISH-mapped, polymorphic STSs are heterozygous in 7 or more of the individuals tested. Since these markers are derived from physically mapped cosmids, genetic linkage analysis with them will facilitate the integration of the developing physical and genetic maps of chromosome 12.

摘要

从一个12号染色体特异性黏粒文库中开发出了21个物理定位的多态性标记。这些标记由包含CA重复序列的序列标签位点(STS)组成,这些位点来源于通过荧光原位杂交(FISH)定位的黏粒克隆。使用了三种确定CA微卫星侧翼序列的方法,其中一种使用简并引物组进行直接序列分析。从CA微卫星侧翼序列中选择适合用于聚合酶链反应(PCR)的寡核苷酸引物对,并测试它们产生独特PCR产物的能力。通过对10名属于人类多态性研究中心(EPH)家系的无关个体进行分型,确定了这些STS作为遗传标记的信息含量。在21个经FISH定位的多态性STS中,有11个在7个或更多测试个体中呈杂合状态。由于这些标记来源于物理定位的黏粒,利用它们进行遗传连锁分析将有助于整合正在构建的12号染色体物理图谱和遗传图谱。

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