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embryonic stem cells

Auxin-Degron System Identifies Immediate Mechanisms of OCT4

[Stem Cell Reports] Researchers developed a rapid protein-level OCT4 depletion system that demonstrated that the immediate downstream response to loss of OCT4 was reduced expression of key pluripotency factors.

Arginine Methylation of METTL14 Promotes RNA N6-Methyladenosine Modification and Endoderm Differentiation of Mouse Embryonic Stem Cells

[Nature Communications] The authors investigated the role of methylation of the core methyltransferase METTL3/METTL14 in m6A regulation. They found that global mRNA m6A levels were greatly decreased in METTL14 R255K mutant mouse ESCs (mESCs) and that that loss of R255me preferentially affected endoderm differentiation in mESCs.

Generation of Clinical-Grade Human Embryonic Stem Cell Line KthES11 according to Japanese Regulations

[Stem Cell Research] Cell line derivation, its propagation and storage of the human embryonic stem cell line, KthES11, were performed without feeders in an animal product-free environment according to current Good Manufacturing Practice standards.

E2F6 Initiates Stable Epigenetic Silencing of Germline Genes during Embryonic Development

[Nature Communications] Researchers demonstrated that the transcription factor E2F6, a member of the polycomb repressive complex 1.6, was critical to target and initiate epigenetic silencing at germline genes in early embryogenesis.

Probing the Signaling Requirements for Naive Human Pluripotency by High-Throughput Chemical Screening

[Cell Reports] The authors reported that MEK1/2 inhibitors could be replaced during maintenance of naive human pluripotency by inhibitors targeting either upstream or downstream kinases. Naive human ESCs maintained under these alternative conditions displayed elevated levels of ERK phosphorylation but retained genome-wide DNA hypomethylation and a transcriptional identity of the pre-implantation epiblast.

AP-1 Is a Temporally Regulated Dual Gatekeeper of Reprogramming to Pluripotency

[Proceedings of the National Academy of Sciences of the United States of America] Scientists examined epigenome remodeling at the onset of human nuclear reprogramming by profiling human fibroblasts after fusion with murine ESCs. Efficient reprogramming of human fibroblasts to iPSCs was achieved by transduction with vectors expressing SOX2, KLF4, and inducible dnAP-1, demonstrating that dnAP-1 can substitute for exogenous human OCT4.

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