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Genome-wide mapping of transcription factor Oct4, Sox2 and Nanog binding-sites in mouse embryonic stem cells Genome Institute of Singapore Department of Biological Sciences National University of Singapore
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ChIP-PET technology to map ES cell specific transcription factors Yijun Ruan / Chia-Lin Wei (Cloning & Sequencing, Genome Institute of Singapore)
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ChIP-PET captures Oct4 binding profile
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Determination of cutoff for ChIP-PET data cutoff
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Oct4 Sox2 Nanog No. of binding sites~1000 ~1000 ~3000 Based on 4 PET overlap as a cutoff.
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Distribution of Oct4 binding sites
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Binding site in gene desert
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Sox2
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Distribution of Nanog binding sites
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Oct4Sox2 de novo prediction of motifs Oct4Sox2 The code for targeting Oct4 to the genome
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Oct4Sox2 Oct4Sox2 1000 Sox2 binding sites Sox2 binding sites contain a prominent Sox2-Oct4 motif de novo prediction of motif
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Question 1: What are the motifs bound by these TFs? Oct4Sox2Nanog Oct4 Sox2 ? Oct4 and Sox2 are primarily recruited to the genome through the joint sox2 oct4 motifs de novo prediction of motifs using the ChIP-PET data
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What are the motifs bound by Nanog?
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Refined using ChIP-PET data Sequences found in EMSA validated probes
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Oct4 positively regulates the expression of novel target genes
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Oct4 negatively regulates the expression of Cdx2 (trophectoderm transcription factor)
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Nanog
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Sox2
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microRNAs targeted by Nanog
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“Core” Target Genes of Oct4, Sox2 and Nanog in mouse ES cells
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Nanog Sox2 Oct4 Configuration of transcription factors interaction with upstream regulatory region
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Co-occupancy of sites by OCt4/Sox2/nanog
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Whole genome maps For Oct4 and Nanog
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Oct4NanogSox2 Mouse vs Human comparison of Oct4, Nanog and Sox2 TFBS
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Comparison between mouse and human Sox2 binding sites Sox2
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Summary Oct4 and Sox2 make use of oct-sox joint motifs for binding (increased specificities?) Nanog’s motif is abundant in the genome Co-targeting of genes by the 3 transcription factors Coordinated regulation The 3 transcription factors can regulate positively and negatively regulate transcription The target genes fall into diverse functional categories DNA response pathway Cellular proliferation Inhibitors of lineage specific genes
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Acknowledgement: Huck Hui Ng Qiang Wu Joon-Lin Chew Yuin-Han Loh Xi Chen Weiwei Zhang Cloning & Sequencing Group Yijun Ruan Chia-Lin Wei Stem Cell Biology Group Bing Lim Paul Robson Larry Stanton Informatics Vega Ken Sung Guillaume Bourque Vlad Leonard Funding: Biomedical Research Council A*STAR National University of Singapore Singapore Millennium Foundation
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Comparison between mouse and human Oct4 binding sites Oct4
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