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Enrichment of meiotic recombination hotspot sequences by avidin capture technology
Author(s) -
Teixeira Daniel Camara,
Zempleni Janos,
Malkaram Sridhar A
Publication year - 2013
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.27.1_supplement.370.5
Subject(s) - oligonucleotide , biology , dna , streptavidin , homologous recombination , microbiology and biotechnology , genetics , computational biology , chemistry , biotin
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 (>;3,000 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 be adopted 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. Grant Funding Source : ARD Hatch, NIFA and NIH.