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使用单向PCR鉴定小鼠微卫星基因座D17Mit23在PCR过程中形成的显著异源双链体。

The use of unilateral PCR to identify prominent heteroduplexes formed during PCR of the mouse microsatellite locus D17Mit23.

作者信息

Erhart Mark A, Kim Taehoon, Crews Gladys M, Pandya Avani

机构信息

Department of Biological Sciences, Chicago State University, 9501 S. King Drive, Chicago, IL 60628, USA.

出版信息

Mol Biotechnol. 2006 May;33(1):37-48. doi: 10.1385/MB:33:1:37.

Abstract

Microsatellite markers are useful tools for understanding the evolutionary history of discrete segments of the mammalian genome. We used the microsatellite marker D17Mit23 to study the portion of the mouse genome known as the t complex, a naturally occurring variant of Chromosome 17. We identified an allelic variant of D17Mit23, which is shared by two forms of the t complex, the t haplotypes t(w2) and t(Lub2). Polymerase chain reaction (PCR) analysis of DNA samples from mice that were heterozygous for either t haplotype resulted in gel patterns with prominent bands of higher molecular weight in addition to the bona-fide D17Mit23 alleles. The appearance of these higher molecular weight bands, although consistent with heteroduplex formation, was not diminished through the use of reconditioning PCR. We used a modified form of asymmetric PCR, called "unilateral PCR," to show that the higher molecular weight bands are heteroduplexes and to identify their constituent strands. Certain microsatellite motifs may be especially prone to the production of prominent heteroduplex products, and this may lead to the erroneous genotyping of DNA samples.

摘要

微卫星标记是理解哺乳动物基因组离散片段进化历史的有用工具。我们使用微卫星标记D17Mit23来研究小鼠基因组中被称为t复合体的部分,它是17号染色体的一种自然发生的变体。我们鉴定出了D17Mit23的一个等位基因变体,它存在于t复合体的两种形式,即t单倍型t(w2)和t(Lub2)中。对任一t单倍型杂合的小鼠的DNA样本进行聚合酶链反应(PCR)分析,除了真正的D17Mit23等位基因外,凝胶图谱上还出现了分子量较高的明显条带。这些分子量较高条带的出现,虽然与异源双链体的形成一致,但通过使用复性PCR并没有减弱。我们使用一种称为“单边PCR”的改良不对称PCR形式,来证明分子量较高的条带是异源双链体,并鉴定其组成链。某些微卫星基序可能特别容易产生明显的异源双链体产物,这可能导致DNA样本的错误基因分型。

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