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izvor podataka: crosbi

The role of GCNA (ACRC) protein in the DNA-protein crosslink repair in zebrafish (CROSBI ID 733706)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Kutnjak, Marin ; Supina Pavić, Christine ; Otten, Cecile ; Popović, Marta The role of GCNA (ACRC) protein in the DNA-protein crosslink repair in zebrafish // Book of Abstracts of the Congress of the Croatian Society of Biochemistry and Molecular Biology "HDBMB22: From Science to Knowledge" / Dulić, Morana ; Sinčić, Nino ; Vrhovac Madunić, Ivana (ur.). Zagreb: Hrvatsko Društvo za Biotehnologiju, 2022. str. 99-99

Podaci o odgovornosti

Kutnjak, Marin ; Supina Pavić, Christine ; Otten, Cecile ; Popović, Marta

engleski

The role of GCNA (ACRC) protein in the DNA-protein crosslink repair in zebrafish

DNA is a molecule in a chemically reactive environment and under these conditions various DNA lesions are constantly formed in cells. Proteins that interact with DNA or are in its proximity can become irreversibly covalently bound to DNA and form lesions called DNA-protein crosslinks (DPCs). DPCs can be induced by exogenous (UV and ionizing radiation, transition metals, chemotherapeutic agents) and endogenous factors (reactive oxygen and nitrogen species, aldehydes, DNA helix alterations). They affect cellular processes that include DNA (DNA replication, transcription, repair, recombination, and chromatin remodeling) and are obstacles to genome stability maintenance. Several groups have characterized the proteins Wss1 in yeast and SPRTN in metazoans as the first identified proteases involved in DPC repair. At the cellular level, impaired DPC repair can lead to DNA double-strand breaks, genomic instability, and consequently cell death, while at the organismal level it can cause cancer, premature aging, and neurodegenerative diseases. Recent studies have shown that there is a second potential DPC protease in metazoans: GCNA (germ cell nuclear acidic) or ACRC (acidic repeat- containing). Phylogenetic analysis of the SprT and WLM domains and structural modeling of the protease cores of SPRTN and GCNA have revealed similarities between these two proteins. The aim of our study was to determine whether GCNA is involved in DPC repair in vivo and whether its putative protease core is important for GCNA function. We used zebrafish (Danio rerio) as a model organism, CRISPR/Cas9 gene manipulation to generate zebrafish mutant strains, and the RADAR (rapid approach to DNA adduct recovery) method to isolate DPCs from mutant embryos. We introduced a mutation in the putative protease active site of GCNA that includes a deletion of E451 (putative catalytic glutamate). Our results showed that the mutant embryos had 100% mortality within the first 24 hours of development due to maternal effect. Primarily, they had an increased total amount of cellular DPCs. Our study demonstrates the importance of GCNA for embryonic development and DPC repair at the organismal level, as well as the importance of the putative protease core for GCNA function.

DNA repair ; DNA-protein crosslinks (DPCs) ; GCNA (ACRC) protease ; CRISPR/Cas9 ; zebrafish

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nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o prilogu

99-99.

2022.

objavljeno

Podaci o matičnoj publikaciji

Book of Abstracts of the Congress of the Croatian Society of Biochemistry and Molecular Biology "HDBMB22: From Science to Knowledge"

Dulić, Morana ; Sinčić, Nino ; Vrhovac Madunić, Ivana

Zagreb: Hrvatsko Društvo za Biotehnologiju

1847-7836

Podaci o skupu

International congress of the Croatian society of biochemistry and molecular biology HDBMB22 "From science to knowledge"

poster

28.09.2022-01.10.2022

Brela, Hrvatska

Povezanost rada

Biologija