Rap1 regulates TIP60 function during fate transition between two-cell-like and pluripotent states

التفاصيل البيبلوغرافية
العنوان: Rap1 regulates TIP60 function during fate transition between two-cell-like and pluripotent states
المؤلفون: Raymond Mario Barry, Olivia Sacco, Amel Mameri, Martin Stojaspal, William Kartsonis, Pooja Shah, Pablo De Ioannes, Ctirad Hofr, Jacques Côté, Agnel Sfeir
المصدر: Genes & Development. 36:313-330
بيانات النشر: Cold Spring Harbor Laboratory, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Mammals, Mice, enzymes and coenzymes (carbohydrates), endocrine system, Genome, Gene Expression Regulation, Telomere-Binding Proteins, Genetics, Animals, Mouse Embryonic Stem Cells, Telomere, Developmental Biology
الوصف: In mammals, the conserved telomere binding protein Rap1 serves a diverse set of nontelomeric functions, including activation of the NF-kB signaling pathway, maintenance of metabolic function in vivo, and transcriptional regulation. Here, we uncover the mechanism by which Rap1 modulates gene expression. Using a separation-of-function allele, we show that Rap1 transcriptional regulation is largely independent of TRF2-mediated binding to telomeres and does not involve direct binding to genomic loci. Instead, Rap1 interacts with the TIP60/p400 complex and modulates its histone acetyltransferase activity. Notably, we show that deletion of Rap1 in mouse embryonic stem cells increases the fraction of two-cell-like cells. Specifically, Rap1 enhances the repressive activity of Tip60/p400 across a subset of two-cell-stage genes, including Zscan4 and the endogenous retrovirus MERVL. Preferential up-regulation of genes proximal to MERVL elements in Rap1-deficient settings implicates these endogenous retroviral elements in the derepression of proximal genes. Altogether, our study reveals an unprecedented link between Rap1 and the TIP60/p400 complex in the regulation of pluripotency.
تدمد: 1549-5477
0890-9369
DOI: 10.1101/gad.349039.121
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::884702b5350f541191267471a43462a1
https://doi.org/10.1101/gad.349039.121
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....884702b5350f541191267471a43462a1
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15495477
08909369
DOI:10.1101/gad.349039.121