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Transcription of Repeats Activates INterferon (TRAIN) in response to chromatin destabilization induced with anti-cancer small molecule

https://doi.org/10.1101/142471
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FACT Disrupts Nucleosome Structure by Binding H2A-H2B with Conserved Peptide Motifs
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Crystal structure of the nucleosome core particle at 2.8 Å resolution
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DNMT3A mutations promote anthracycline resistance in acute myeloid leukemia via impaired nucleosome remodeling
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A universal classification of eukaryotic transposable elements implemented in Repbase
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Single-base resolution mapping of H1–nucleosome interactions and 3D organization of the nucleosome
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p53 cooperates with DNA methylation and a suicidal interferon response to maintain epigenetic silencing of repeats and noncoding RNAs
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Structural insights into the histone H1-nucleosome complex
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Interaction of FACT, SSRP1, and the High Mobility Group (HMG) Domain of SSRP1 with DNA Damaged by the Anticancer Drug Cisplatin
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Identification of a Functional Network of Human Epigenetic Silencing Factors
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Protein Kinase CK2 Phosphorylates the High Mobility Group Domain Protein SSRP1, Inducing the Recognition of UV-damaged DNA
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The Histone Chaperone FACT: Structural Insights and Mechanisms for Nucleosome Reorganization
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Sperm Chromatin
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Enhanced Tumor Development in Mice Lacking a Functional Type I Interferon Receptor
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The Role of Nuclear Factor κB in the Interferon Response
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CENP-H–containing Complex Facilitates Centromere Deposition of CENP-A in Cooperation with FACT and CHD1
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Transcription factors induced by interferons α and γ
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Silencing of IFN-stimulated gene transcription is regulated by histone H1 and its chaperone TAF-I
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FACT is a sensor of DNA torsional stress in eukaryotic cells
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Anticancer drug candidate CBL0137, which inhibits histone chaperone FACT, is efficacious in preclinical orthotopic models of temozolomide-responsive and -resistant glioblastoma
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Integrated molecular mechanism directing nucleosome reorganization by human FACT
inferredcites →https://doi.org/10.1101/gad.275073.115openalex-snapshot
The CENP-T/-W complex is a binding partner of the histone chaperone FACT
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FACT Facilitates Transcription-Dependent Nucleosome Alteration
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Transgenerational inheritance: Models and mechanisms of non–DNA sequence–based inheritance
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Curaxins: Anticancer Compounds That Simultaneously Suppress NF-κB and Activate p53 by Targeting FACT
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Pharmacological Targeting of the Histone Chaperone Complex FACT Preferentially Eliminates Glioblastoma Stem Cells and Prolongs Survival in Preclinical Models
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Targeting FACT Complex Suppresses Mammary Tumorigenesis in Her2 / neu Transgenic Mice
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Advances in understanding genome maintenance
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The Mammalian Blood-Testis Barrier: Its Biology and Regulation
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The NF-κB activation pathways, emerging molecular targets for cancer prevention and therapy
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Level of FACT defines the transcriptional landscape and aggressive phenotype of breast cancer cells
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Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells
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Synthetic and Natural Immunomodulators Acting as Interferon Inducers
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Pharmacological Activation of p53 in Cancer Cells
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Stabilization of Nucleosomes by Histone Tails and by FACT Revealed by spFRET Microscopy
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The DNA Damage Response Induces IFN
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Complex mutual regulation of facilitates chromatin transcription (FACT) subunits on both mRNA and protein levels in human cells
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