Literature DB >> 23270922

Enrichment of meiotic recombination hotspot sequences by avidin capture technology.

Daniel Camara Teixeira1, Sridhar A Malkaram, Janos Zempleni.   

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.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 23270922      PMCID: PMC3563735          DOI: 10.1016/j.gene.2012.12.042

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  13 in total

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6.  PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice.

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7.  Drive against hotspot motifs in primates implicates the PRDM9 gene in meiotic recombination.

Authors:  Simon Myers; Rory Bowden; Afidalina Tumian; Ronald E Bontrop; Colin Freeman; Tammie S MacFie; Gil McVean; Peter Donnelly
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8.  Prdm9 controls activation of mammalian recombination hotspots.

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Journal:  Science       Date:  2009-12-31       Impact factor: 47.728

9.  Biotinylation of histones represses transposable elements in human and mouse cells and cell lines and in Drosophila melanogaster.

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