2014
HP1B-dependent recruitment of UBF1 to irradiated chromatin occurs simultaneously with CPDs
STIXOVÁ, Lenka, Petra SEHNALOVÁ, Soňa LEGARTOVÁ, Jana SUCHÁNKOVÁ, Tereza HRUŠKOVÁ et. al.Základní údaje
Originální název
HP1B-dependent recruitment of UBF1 to irradiated chromatin occurs simultaneously with CPDs
Autoři
STIXOVÁ, Lenka (203 Česká republika), Petra SEHNALOVÁ (203 Česká republika), Soňa LEGARTOVÁ (703 Slovensko), Jana SUCHÁNKOVÁ (203 Česká republika), Tereza HRUŠKOVÁ (203 Česká republika), Stanislav KOZUBEK (203 Česká republika), Dmitry SOROKIN (643 Rusko, garant, domácí), Pavel MATULA (203 Česká republika, domácí), Ivan RAŠKA (203 Česká republika), Aleš KOVAŘÍK (203 Česká republika), Jaroslav FULNEČEK (203 Česká republika) a Eva BÁRTOVÁ (203 Česká republika)
Vydání
Epigenetics & Chromatin, BioMed Central, 2014, 1756-8935
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
Genetika a molekulární biologie
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 5.333
Kód RIV
RIV/00216224:14330/14:00074061
Organizační jednotka
Fakulta informatiky
UT WoS
000347931500001
Klíčová slova anglicky
DNA-damage response; DNA repair; Irradiation; Live-cell studies; Nucleolus; UBF1
Změněno: 28. 4. 2015 13:35, doc. RNDr. Pavel Matula, Ph.D.
Anotace
V originále
Background. The repair of spontaneous and induced DNA lesions is a multistep process. Depending on the type of injury, damaged DNA is recognized by many proteins specifically involved in distinct DNA repair pathways. Results. We analyzed the DNA-damage response after ultraviolet A (UVA) and gamma irradiation of mouse embryonic fibroblasts and focused on upstream binding factor 1 (UBF1), a key protein in the regulation of ribosomal gene transcription. We found that UBF1, but not nucleolar proteins RPA194, TCOF, or fibrillarin, was recruited to UVA-irradiated chromatin concurrently with an increase in heterochromatin protein 1-betta (HP1betta) level. Moreover, Förster Resonance Energy Transfer (FRET) confirmed interaction between UBF1 and HP1betta that was dependent on a functional chromo shadow domain of HP1betta. Thus, overexpression of HP1betta with a deleted chromo shadow domain had a dominant-negative effect on UBF1 recruitment to UVA-damaged chromatin. Transcription factor UBF1 also interacted directly with DNA inside the nucleolus but no interaction of UBF1 and DNA was confirmed outside the nucleolus, where UBF1 recruitment to DNA lesions appeared simultaneously with cyclobutane pyrimidine dimers; this occurrence was cell-cycle-independent. Conclusions. We propose that the simultaneous presence and interaction of UBF1 and HP1betta at DNA lesions is activated by the presence of cyclobutane pyrimidine dimers and mediated by the chromo shadow domain of HP1betta. This might have functional significance for nucleotide excision repair.
Návaznosti
CZ.1.07/2.3.00/30.0030, interní kód MU |
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GBP302/12/G157, projekt VaV |
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