Rap1 regulates TIP60 function during fate transition between two-cell-like and pluripotent states
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F22%3A00559188" target="_blank" >RIV/68081707:_____/22:00559188 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14310/22:00125447
Result on the web
<a href="http://genesdev.cshlp.org/content/36/5-6/313" target="_blank" >http://genesdev.cshlp.org/content/36/5-6/313</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1101/gad.349039.121" target="_blank" >10.1101/gad.349039.121</a>
Alternative languages
Result language
angličtina
Original language name
Rap1 regulates TIP60 function during fate transition between two-cell-like and pluripotent states
Original language description
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 upregulation 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.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10601 - Cell biology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Genes and Development
ISSN
0890-9369
e-ISSN
1549-5477
Volume of the periodical
36
Issue of the periodical within the volume
5-6
Country of publishing house
US - UNITED STATES
Number of pages
18
Pages from-to
313-330
UT code for WoS article
000821506300006
EID of the result in the Scopus database
2-s2.0-85127841683