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DUX4 regulates oocyte to embryo transition in human

biorxiv. 2019; 
Sanna Vuoristo, Christel Hydén-Granskog, Masahito Yoshihara, Lisa Gawriyski, Anastassius Damdimopoulos, Shruti Bhagat, Kosuke Hashimoto, Kaarel Krjutškov, Sini Ezer, Priit Paluoja, Karolina Lundin, Pauliina Paloviita, Gaëlle Recher, Vipin Ranga, Tomi Airenne, Mahlet Tamirat, Eeva-Mari Jouhilahti, Timo Otonkoski, Juha S. Tapanainen, Hideya Kawaji, Yasuhiro Murakawa, Thomas R. Bürglin, Markku Varjosalo, Mark S. Johnson, Timo Tuuri, Shintaro Katayama, Juha Kere
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Molecular Biology Reagents The full-length DUX4 (NM_001293798.2) was synthesized and cloned between the SalI and BamHI sites of the pB-tight-hMAFA-ires-EmGFP-pA-PGK-Puro vector (a kind gift from Diego Balboa, Biomedicum Stem Cell Centre) at GenScript (Genscript, NJ, USA). Get A Quote

摘要

In oocyte to embryo transition, the fertilized oocyte undergoes final maturation and the embryo genome is gradually activated during the first three cell divisions. How this transition is coordinated and which factors drive the processes in humans is largely unknown. Here we studied the role of the double homeodomain transcription factor DUX4 in regulating the human oocyte to embryo transition. DUX4 knockdown zygotes show delayed transcriptome reprogramming during the first three days after fertilization. Our combined experimental approaches allowed integrated analysis on the transcriptome, chromatin, and proteome data in human embryos or a DUX4 expressing human embryonic stem cell model. We conclude that DUX4 ... More

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