TRF1 negotiates TTAGGG repeat-associated replication problems by recruiting the BLM helicase and the TPP1/POT1 repressor of ATR signaling
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
R01 AG016642
NIA NIH HHS - United States
R37 GM049046
NIGMS NIH HHS - United States
5R37GM49046
NIGMS NIH HHS - United States
5R01AG16642
NIA NIH HHS - United States
PubMed
25344324
PubMed Central
PMC4233241
DOI
10.1101/gad.251611.114
PII: gad.251611.114
Knihovny.cz E-zdroje
- Klíčová slova
- BLM, G quadruplex, TRF1, replication, shelterin, telomere,
- MeSH
- aktivace enzymů MeSH
- ATM protein metabolismus MeSH
- DNA vazebné proteiny metabolismus MeSH
- genový knockout MeSH
- helikasy RecQ genetika metabolismus MeSH
- kultivované buňky MeSH
- mikrosatelitní repetice genetika MeSH
- mutace MeSH
- protein TRF1 genetika metabolismus MeSH
- proteiny vázající telomery genetika metabolismus MeSH
- replikace DNA genetika MeSH
- serinové proteasy genetika metabolismus MeSH
- shelterinový komplex MeSH
- signální transdukce MeSH
- telomery genetika MeSH
- vazba proteinů MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- Acd protein, mouse MeSH Prohlížeč
- ATM protein MeSH
- Atr protein, mouse MeSH Prohlížeč
- Bloom syndrome protein MeSH Prohlížeč
- DNA vazebné proteiny MeSH
- helikasy RecQ MeSH
- POT1 protein, mouse MeSH Prohlížeč
- protein TRF1 MeSH
- proteiny vázající telomery MeSH
- serinové proteasy MeSH
- shelterinový komplex MeSH
- Tinf2 protein, mouse MeSH Prohlížeč
The semiconservative replication of telomeres is facilitated by the shelterin component TRF1. Without TRF1, replication forks stall in the telomeric repeats, leading to ATR kinase signaling upon S-phase progression, fragile metaphase telomeres that resemble the common fragile sites (CFSs), and the association of sister telomeres. In contrast, TRF1 does not contribute significantly to the end protection functions of shelterin. We addressed the mechanism of TRF1 action using mouse conditional knockouts of BLM, TRF1, TPP1, and Rap1 in combination with expression of TRF1 and TIN2 mutants. The data establish that TRF1 binds BLM to facilitate lagging but not leading strand telomeric DNA synthesis. As the template for lagging strand telomeric DNA synthesis is the TTAGGG repeat strand, TRF1-bound BLM is likely required to remove secondary structures formed by these sequences. In addition, the data establish that TRF1 deploys TIN2 and the TPP1/POT1 heterodimers in shelterin to prevent ATR during telomere replication and repress the accompanying sister telomere associations. Thus, TRF1 uses two distinct mechanisms to promote replication of telomeric DNA and circumvent the consequences of replication stress. These data are relevant to the expression of CFSs and provide insights into TIN2, which is compromised in dyskeratosis congenita (DC) and related disorders.
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G4Hunter web application: a web server for G-quadruplex prediction