KAT2-mediated PLK4 acetylation contributes to genomic stability by preserving centrosome number.
Fiche publication
Date publication
janvier 2017
Journal
Molecular & cellular oncology
Auteurs
Membres identifiés du Cancéropôle Est :
Dr TORA Laszlo
Tous les auteurs :
Fournier M, Tora L
Lien Pubmed
Résumé
We have recently identified the first human lysine (K) acetyltransferase 2A and 2B (called KAT2A/2B; known also as GCN5/PCAF, respectively)-dependent acetylome and revealed a mechanism by which KAT2A/2B-mediated acetylation of serine/threonine polo-like kinase 4 (PLK4) maintains correct centrosome number in human cells, therefore contributing to the maintenance of genome stability.(1).
Référence
Mol Cell Oncol. 2017 ;4(2):e1270391