2023
The SAGA histone acetyltransferase module targets SMC5/6 to specific genes
MAHRÍK, Lenka, Barbora ŠTEFANOVIE, Anna MARESOVA, Jarmila PRINCOVA, Peter KOLESÁR et. al.Základní údaje
Originální název
The SAGA histone acetyltransferase module targets SMC5/6 to specific genes
Autoři
MAHRÍK, Lenka (703 Slovensko, domácí), Barbora ŠTEFANOVIE (703 Slovensko, domácí), Anna MARESOVA (203 Česká republika), Jarmila PRINCOVA (203 Česká republika), Peter KOLESÁR (703 Slovensko, domácí), Edit LELKES (703 Slovensko, domácí), Celline FAUX (250 Francie), Dominique HELMLINGER (250 Francie), Martin PREVOROVSKY (203 Česká republika) a Jan PALEČEK (203 Česká republika, garant, domácí)
Vydání
EPIGENETICS & CHROMATIN, LONDON, BMC, 2023, 1756-8935
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.900 v roce 2022
Kód RIV
RIV/00216224:14310/23:00130526
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000944569400001
Klíčová slova anglicky
Genetic and protein-protein interactions; SMC5/6 complex; Nse3 KITE; SAGA histone acetyltransferase module; Gcn5; Ada2; Chromatin accessibility; DNA repair; rDNA; Gene regions
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 5. 3. 2024 09:23, Mgr. Eva Dubská
Anotace
V originále
Structural Maintenance of Chromosomes (SMC) complexes are molecular machines driving chromatin organization at higher levels. In eukaryotes, three SMC complexes (cohesin, condensin and SMC5/6) play key roles in cohesion, condensation, replication, transcription and DNA repair. Their physical binding to DNA requires accessible chromatin. We performed a genetic screen in fission yeast to identify novel factors required for SMC5/6 binding to DNA. We identified 79 genes of which histone acetyltransferases (HATs) were the most represented. Genetic and phenotypic analyses suggested a particularly strong functional relationship between the SMC5/6 and SAGA complexes. Furthermore, several SMC5/6 subunits physically interacted with SAGA HAT module components Gcn5 and Ada2. As Gcn5-dependent acetylation facilitates the accessibility of chromatin to DNA-repair proteins, we first analysed the formation of DNA-damage-induced SMC5/6 foci in the Delta gcn5 mutant. The SMC5/6 foci formed normally in Delta gcn5, suggesting SAGA-independent SMC5/6 localization to DNA-damaged sites. Next, we used Nse4-FLAG chromatin-immunoprecipitation (ChIP-seq) analysis in unchallenged cells to assess SMC5/6 distribution. A significant portion of SMC5/6 accumulated within gene regions in wild-type cells, which was reduced in Delta gcn5 and Delta ada2 mutants. The drop in SMC5/6 levels was also observed in gcn5-E191Q acetyltransferase-dead mutant. Our data show genetic and physical interactions between SMC5/6 and SAGA complexes. The ChIP-seq analysis suggests that SAGA HAT module targets SMC5/6 to specific gene regions and facilitates their accessibility for SMC5/6 loading.
Návaznosti
LM2018132, projekt VaV |
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LTC20033, projekt VaV |
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MUNI/R/1142/2021, interní kód MU |
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MUNI/R/1262/2022, interní kód MU |
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