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利用亲和素捕获技术富集减数分裂重组热点序列。

Enrichment of meiotic recombination hotspot sequences by avidin capture technology.

机构信息

Department of Nutrition and Health Sciences, University of Nebraska-Lincoln, Lincoln, NE 68583-0806, USA.

出版信息

Gene. 2013 Mar 1;516(1):101-6. doi: 10.1016/j.gene.2012.12.042. Epub 2012 Dec 24.

Abstract

About 40% of the hotspots for meiotic recombination contain the degenerate consensus sequence 5'-CCNCCNTNNCCNC-3'. Here we present a novel protocol for enriching hotspot sequences from digested genomic DNA by using biotinylated oligonucleotides and streptavidin-coated magnetic beads. The captured hotspots can be released by simple digestion with restriction enzymes for subsequent characterization by second generation sequencing or PCR. The capture protocol specifically enriches hotspot sequences, judged by using fluorophore-conjugated synthetic oligonucleotides and synthetic double-stranded oligonucleotides in combination with PCR. The capture protocol enriches single-stranded DNA, denatured double-stranded DNA, and large fragments (>3000 bp) of digested plasmid DNA with good efficacy. No false positive and false negatives were detected when enriching digested DNA from human cell cultures and primary human cells. The protocol can probably be adapted to enriching sequences other than the hotspot sequence by altering the sequence in the capture oligonucleotide. We intend to apply this protocol in studies assessing effects of micronutrient status on meiotic recombination events in human sperm.

摘要

约 40%的减数分裂重组热点包含退化的共有序列 5'-CCNCCNTNNCCNC-3'。在这里,我们提出了一种从消化的基因组 DNA 中富集热点序列的新方案,该方案使用生物素化寡核苷酸和链霉亲和素包被的磁珠。通过简单的酶切消化可以释放捕获的热点,然后进行第二代测序或 PCR 进行后续分析。该捕获方案通过使用荧光标记的合成寡核苷酸和合成双链寡核苷酸与 PCR 相结合,特异性地富集热点序列。该捕获方案对单链 DNA、变性双链 DNA 以及消化的质粒 DNA 的大片段(>3000 bp)具有良好的富集效果。从人细胞培养物和原代人细胞中富集消化的 DNA 时,没有检测到假阳性和假阴性。通过改变捕获寡核苷酸中的序列,该方案可能适用于富集除热点序列以外的序列。我们打算在评估微量营养素状态对人类精子减数分裂重组事件的影响的研究中应用该方案。

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