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PRDM9 forms a multiprotein complex tethering recombination hotspots to the chromosomal axis

Emil D. Parvanov, Hui Tian, Timothy Billings, Ruth L. Saxl, Catrina Spruce, Rakesh Aithal, Lumir Krejci, Kenneth Paigen, View ORCID ProfilePetko M. Petkov
doi: https://doi.org/10.1101/056713
Emil D. Parvanov
aCenter for Genome Dynamics, The Jackson Laboratory, Bar Harbor, ME, USA, 04609
bDepartment of Biology, Masaryk University, Brno, Czech Republic
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Hui Tian
aCenter for Genome Dynamics, The Jackson Laboratory, Bar Harbor, ME, USA, 04609
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Timothy Billings
aCenter for Genome Dynamics, The Jackson Laboratory, Bar Harbor, ME, USA, 04609
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Ruth L. Saxl
aCenter for Genome Dynamics, The Jackson Laboratory, Bar Harbor, ME, USA, 04609
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Catrina Spruce
aCenter for Genome Dynamics, The Jackson Laboratory, Bar Harbor, ME, USA, 04609
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Rakesh Aithal
bDepartment of Biology, Masaryk University, Brno, Czech Republic
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Lumir Krejci
bDepartment of Biology, Masaryk University, Brno, Czech Republic
cNational Centre for Biomolecular Research, Masaryk University, Brno, Czech Republic 625 00
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  • For correspondence: petko.petkov@jax.org lkrejci@chemi.muni.cz
Kenneth Paigen
aCenter for Genome Dynamics, The Jackson Laboratory, Bar Harbor, ME, USA, 04609
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Petko M. Petkov
aCenter for Genome Dynamics, The Jackson Laboratory, Bar Harbor, ME, USA, 04609
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  • ORCID record for Petko M. Petkov
  • For correspondence: petko.petkov@jax.org lkrejci@chemi.muni.cz
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ABSTRACT

In mammals, meiotic recombination occurs at 1-2 kb genomic regions termed hotspots, whose positions and activities are determined by PRDM9, a DNA-binding histone methyltransferase. We now show that the KRAB domain of PRDM9 forms complexes with additional proteins to allow hotspots to proceed into the next phase of recombination. By a combination of yeast-two hybrid assay, in vitro binding, and co-immunoprecipitation from mouse spermatocytes, we identified four proteins that directly interact with PRDM9’s KRAB domain, namely CXXC1, EWSR1, EHMT2, and CDYL. These proteins are co-expressed in spermatocytes at the early stages of meiotic prophase I, the limited period when PRDM9 is expressed. We also detected association of PRDM9-bound complexes with the meiotic cohesin REC8 and the synaptonemal complex proteins SYCP3 and SYCP1. Our results suggest a model in which PRDM9-bound hotspot DNA is brought to the chromosomal axis by the action of these proteins, ensuring the proper chromatin and spatial environment for subsequent recombination events.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted September 16, 2016.
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PRDM9 forms a multiprotein complex tethering recombination hotspots to the chromosomal axis
Emil D. Parvanov, Hui Tian, Timothy Billings, Ruth L. Saxl, Catrina Spruce, Rakesh Aithal, Lumir Krejci, Kenneth Paigen, Petko M. Petkov
bioRxiv 056713; doi: https://doi.org/10.1101/056713
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PRDM9 forms a multiprotein complex tethering recombination hotspots to the chromosomal axis
Emil D. Parvanov, Hui Tian, Timothy Billings, Ruth L. Saxl, Catrina Spruce, Rakesh Aithal, Lumir Krejci, Kenneth Paigen, Petko M. Petkov
bioRxiv 056713; doi: https://doi.org/10.1101/056713

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