A defined Oct4 level governs cell state transitions of pluripotency entry and differentiation into all embryonic lineages

Oct4 is considered a master transcription factor for pluripotent cell self-renewal, but its biology remains poorly understood. Here, we investigated the role of Oct4 using the process of induced pluripotency. We found that a defined embryonic stem cell (ESC) level of Oct4 is required for pluripotency entry. However, once pluripotency is established, the Oct4 level can be decreased up to sevenfold without loss of self-renewal. Unexpectedly, cells constitutively expressing Oct4 at an ESC level robustly differentiated into all embryonic lineages and germline. In contrast, cells with low Oct4 levels were deficient in differentiation, exhibiting expression of naive pluripotency genes in the absence of pluripotency culture requisites. The restoration of Oct4 expression to an ESC level rescued the ability of these to restrict naive pluripotent gene expression and to differentiate. In conclusion, a defined Oct4 level controls the establishment of naive pluripotency as well as commitment to all embryonic lineages.

[1]  J. Miyazaki,et al.  Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells , 2000, Nature Genetics.

[2]  J. Miyazaki,et al.  Phenotypic Complementation Establishes Requirements for Specific POU Domain and Generic Transactivation Function of Oct-3/4 in Embryonic Stem Cells , 2002, Molecular and Cellular Biology.

[3]  Pan Du,et al.  lumi: a pipeline for processing Illumina microarray , 2008, Bioinform..

[4]  Austin G Smith,et al.  JAK/STAT3 signalling is sufficient and dominant over antagonistic cues for the establishment of naive pluripotency , 2012, Nature Communications.

[5]  B. Doble,et al.  The ground state of embryonic stem cell self-renewal , 2008, Nature.

[6]  Yoshiakira Kanai,et al.  Depletion of definitive gut endoderm in Sox17-null mutant mice. , 2002, Development.

[7]  J. Nichols,et al.  Nanog safeguards pluripotency and mediates germline development , 2007, Nature.

[8]  H. Schöler,et al.  Germline regulatory element of Oct-4 specific for the totipotent cycle of embryonal cells. , 1996, Development.

[9]  K. Okamoto,et al.  A novel octamer binding transcription factor is differentially expressed in mouse embryonic cells , 1990, Cell.

[10]  Alexei A. Sharov,et al.  Functional Heterogeneity of Embryonic Stem Cells Revealed through Translational Amplification of an Early Endodermal Transcript , 2010, PLoS biology.

[11]  Gonçalo Castelo-Branco,et al.  Nanog Overcomes Reprogramming Barriers and Induces Pluripotency in Minimal Conditions , 2011, Current Biology.

[12]  Marcos J. Araúzo-Bravo,et al.  Direct reprogramming of human neural stem cells by OCT4 , 2009, Nature.

[13]  Hitoshi Niwa,et al.  A parallel circuit of LIF signalling pathways maintains pluripotency of mouse ES cells , 2009, Nature.

[14]  K. Kaestner,et al.  Postimplantation expression patterns indicate a role for the mouse forkhead/HNF-3 alpha, beta and gamma genes in determination of the definitive endoderm, chordamesoderm and neuroectoderm. , 1993, Development.

[15]  Nicola Festuccia,et al.  Esrrb Is a Direct Nanog Target Gene that Can Substitute for Nanog Function in Pluripotent Cells , 2012, Cell stem cell.

[16]  H. Schöler,et al.  Oct‐4: a germline‐specific transcription factor mapping to the mouse t‐complex. , 1990, The EMBO journal.

[17]  R. Lovell-Badge,et al.  Multipotent cell lineages in early mouse development depend on SOX2 function. , 2003, Genes & development.

[18]  H. Niwa,et al.  Identification and characterization of subpopulations in undifferentiated ES cell culture , 2008, Development.

[19]  Peter W. J. Rigby,et al.  A POU-domain transcription factor in early stem cells and germ cells of the mammalian embryo , 1990, Nature.

[20]  W. Huber,et al.  Model-based variance-stabilizing transformation for Illumina microarray data , 2008, Nucleic acids research.

[21]  Marcos J. Araúzo-Bravo,et al.  Oct4-Induced Pluripotency in Adult Neural Stem Cells , 2009, Cell.

[22]  F. Tang,et al.  Dynamic equilibrium and heterogeneity of mouse pluripotent stem cells with distinct functional and epigenetic states. , 2008, Cell stem cell.

[23]  Qi Zhou,et al.  Brief Report: Combined Chemical Treatment Enables Oct4‐Induced Reprogramming from Mouse Embryonic Fibroblasts , 2011, Stem cells.

[24]  M. Trotter,et al.  Pluripotency factors regulate definitive endoderm specification through eomesodermin. , 2011, Genes & development.

[25]  Weiqi Zhang,et al.  Generation of iPSCs from mouse fibroblasts with a single gene, Oct4, and small molecules , 2011, Cell Research.

[26]  Jennifer Nichols,et al.  Promotion of Reprogramming to Ground State Pluripotency by Signal Inhibition , 2008, PLoS biology.

[27]  D. Wilkinson,et al.  Expression pattern of the mouse T gene and its role in mesoderm formation , 1990, Nature.

[28]  H. Schöler,et al.  Formation of Pluripotent Stem Cells in the Mammalian Embryo Depends on the POU Transcription Factor Oct4 , 1998, Cell.

[29]  Ryoichiro Kageyama,et al.  The cyclic gene Hes1 contributes to diverse differentiation responses of embryonic stem cells. , 2009, Genes & development.

[30]  K. Downs Systematic localization of oct‐3/4 to the gastrulating mouse conceptus suggests manifold roles in mammalian development , 2008, Developmental dynamics : an official publication of the American Association of Anatomists.

[31]  J. Nichols,et al.  Oct4 and LIF/Stat3 additively induce Krüppel factors to sustain embryonic stem cell self-renewal. , 2009, Cell stem cell.

[32]  J. Nichols,et al.  Naive and primed pluripotent states. , 2009, Cell stem cell.

[33]  Gordon K Smyth,et al.  Statistical Applications in Genetics and Molecular Biology Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments , 2011 .

[34]  Matt Thomson,et al.  Pluripotency Factors in Embryonic Stem Cells Regulate Differentiation into Germ Layers , 2011, Cell.

[35]  J. Nichols,et al.  Functional Expression Cloning of Nanog, a Pluripotency Sustaining Factor in Embryonic Stem Cells , 2003, Cell.

[36]  Austin G Smith,et al.  Conversion of embryonic stem cells into neuroectodermal precursors in adherent monoculture , 2003, Nature Biotechnology.

[37]  L. Staudt,et al.  Transcriptional activation by Oct-3: evidence for a specific role of the POU-specific domain in mediating functional interaction with Oct-1. , 1996, Nucleic acids research.