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Publication : Transient upregulation of IRF1 during exit from naive pluripotency confers viral protection.

First Author  Romeike M Year  2022
Journal  EMBO Rep Volume  23
Issue  9 Pages  e55375
PubMed ID  35852463 Mgi Jnum  J:328947
Mgi Id  MGI:7341312 Doi  10.15252/embr.202255375
Citation  Romeike M, et al. (2022) Transient upregulation of IRF1 during exit from naive pluripotency confers viral protection. EMBO Rep 23(9):e55375
abstractText  Stem cells intrinsically express a subset of genes which are normally associated with interferon stimulation and the innate immune response. However, the expression of these interferon-stimulated genes (ISG) in stem cells is independent from external stimuli such as viral infection. Here, we show that the interferon regulatory factor 1, Irf1, is directly controlled by the murine formative pluripotency gene regulatory network and transiently upregulated during the transition from naive to formative pluripotency. IRF1 binds to regulatory regions of a conserved set of ISGs and is required for their faithful expression upon exit from naive pluripotency. We show that in the absence of IRF1, cells exiting the naive pluripotent stem cell state are more susceptible to viral infection. Irf1 therefore acts as a link between the formative pluripotency network, regulation of innate immunity genes, and defense against viral infections during formative pluripotency.
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