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; Barbora ŠTEFANOVIE; Anna MARESOVA; Jarmila PRINCOVA; Peter KOLESÁR; Edit LELKES; Celline FAUX; Dominique HELMLINGER; Martin PREVOROVSKY a Jan PALEČEK
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: 4.200
Kód RIV
RIV/00216224:14310/23:00130526
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000944569400001
EID Scopus
2-s2.0-85148114883
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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