Broad histone H3K4me3 domains in mouse oocytes modulate maternal-to-zygotic transition

John Arne Dahl (), Inkyung Jung, Håvard Aanes, Gareth D. Greggains, Adeel Manaf, Mads Lerdrup, Guoqiang Li, Samantha Kuan, Bin Li, Ah Young Lee, Sebastian Preissl, Ingunn Jermstad, Mads Haugland Haugen, Rajikala Suganthan, Magnar Bjørås, Klaus Hansen, Knut Tomas Dalen, Peter Fedorcsak, Bing Ren () and Arne Klungland ()
Additional contact information
John Arne Dahl: Oslo University Hospital
Inkyung Jung: Ludwig Institute for Cancer Research
Håvard Aanes: Oslo University Hospital
Gareth D. Greggains: Section for Reproductive Medicine, Oslo University Hospital
Adeel Manaf: Oslo University Hospital
Mads Lerdrup: The Biotech Research and Innovation Centre and Centre for Epigenetics, University of Copenhagen
Guoqiang Li: Ludwig Institute for Cancer Research
Samantha Kuan: Ludwig Institute for Cancer Research
Bin Li: Ludwig Institute for Cancer Research
Ah Young Lee: Ludwig Institute for Cancer Research
Sebastian Preissl: Ludwig Institute for Cancer Research
Ingunn Jermstad: Norwegian Transgenic Centre, Institute of Basic Medical Sciences, University of Oslo
Mads Haugland Haugen: Institute for Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital
Rajikala Suganthan: Oslo University Hospital
Magnar Bjørås: Oslo University Hospital
Klaus Hansen: The Biotech Research and Innovation Centre and Centre for Epigenetics, University of Copenhagen
Knut Tomas Dalen: Norwegian Transgenic Centre, Institute of Basic Medical Sciences, University of Oslo
Peter Fedorcsak: Section for Reproductive Medicine, Oslo University Hospital
Bing Ren: Ludwig Institute for Cancer Research
Arne Klungland: Oslo University Hospital

Nature, 2016, vol. 537, issue 7621, 548-552

Abstract: Three papers in this issue of Nature use highly sensitive ChIP–seq assays to describe the dynamic patterns of histone modifications during early mouse embryogenesis, showing that oocytes have a distinctive epigenome and providing insights into how the maternal gene expression program transitions to the zygotic program.

Date: 2016
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DOI: 10.1038/nature19360

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