Protein Phosphatase 4 Is Required for Centrobin Function in DNA Damage Repair

Genome stability in human cells relies on the efficient repair of double-stranded DNA breaks, which is mainly achieved by homologous recombination (HR). Among the regulators of various cellular functions, Protein phosphatase 4 (PP4) plays a pivotal role in coordinating cellular response to DNA damag...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Réthi-Nagy Zsuzsánna
Ábrahám Edit
Sinka Rita
Juhász Szilvia
Lipinszki Zoltán
Dokumentumtípus: Cikk
Megjelent: 2023
Sorozat:CELLS 12 No. 18
Tárgyszavak:
doi:10.3390/cells12182219

mtmt:34129677
Online Access:http://publicatio.bibl.u-szeged.hu/34613
LEADER 02196nab a2200265 i 4500
001 publ34613
005 20240912140121.0
008 240912s2023 hu o 000 eng d
022 |a 2073-4409 
024 7 |a 10.3390/cells12182219  |2 doi 
024 7 |a 34129677  |2 mtmt 
040 |a SZTE Publicatio Repozitórium  |b hun 
041 |a eng 
100 2 |a Réthi-Nagy Zsuzsánna 
245 1 0 |a Protein Phosphatase 4 Is Required for Centrobin Function in DNA Damage Repair  |h [elektronikus dokumentum] /  |c  Réthi-Nagy Zsuzsánna 
260 |c 2023 
300 |a 17 
490 0 |a CELLS  |v 12 No. 18 
520 3 |a Genome stability in human cells relies on the efficient repair of double-stranded DNA breaks, which is mainly achieved by homologous recombination (HR). Among the regulators of various cellular functions, Protein phosphatase 4 (PP4) plays a pivotal role in coordinating cellular response to DNA damage. Meanwhile, Centrobin (CNTRB), initially recognized for its association with centrosomal function and microtubule dynamics, has sparked interest due to its potential contribution to DNA repair processes. In this study, we investigate the involvement of PP4 and its interaction with CNTRB in HR-mediated DNA repair in human cells. Employing a range of experimental strategies, we investigate the physical interaction between PP4 and CNTRB and shed light on the importance of two specific motifs in CNTRB, the PP4-binding FRVP and the ATR kinase recognition SQ sequences, in the DNA repair process. Moreover, we examine cells depleted of PP4 or CNTRB and cells harboring FRVP and SQ mutations in CNTRB, which result in similar abnormal chromosome morphologies. This phenomenon likely results from the impaired resolution of Holliday junctions, which serve as crucial intermediates in HR. Taken together, our results provide new insights into the intricate mechanisms of PP4 and CNTRB-regulated HR repair and their interrelation. 
650 4 |a Biológiai tudományok 
700 0 1 |a Ábrahám Edit  |e aut 
700 0 1 |a Sinka Rita  |e aut 
700 0 1 |a Juhász Szilvia  |e aut 
700 0 1 |a Lipinszki Zoltán  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/34613/1/rethi_nagy_et_al_2023.pdf  |z Dokumentum-elérés