ATP-dependent nucleosome-remodeling enzymes and covalent modifiers of chromatin set the functional state of chromatin. However, how these enzymatic activities are coordinated in the nucleus is largely unknown. We found that the evolutionary conserved nucleosome-remodeling ATPase ISWI and the poly-ADP-ribose polymerase PARP genetically interact. We present evidence showing that ISWI is target of poly-ADP-ribosylation. Poly-ADP-ribosylation counteracts ISWI function in vitro and in vivo. Our work suggests that ISWI is a physiological target of PARP and that poly-ADP-ribosylation can be a new, important post-translational modification regulating the activity of ATP-dependent nucleosome remodelers.
SALA A, LA ROCCA G, BURGIO G, KOTOVA E, DI GESU' D, COLLESANO M, et al. (2008). The Nucleosome-Remodeling ATPase ISWI is Regulated by poly-ADP-ribosylation. PLOS BIOLOGY, 6(10), 2329-2342 [10.1371/journal.pbio.0060252].
The Nucleosome-Remodeling ATPase ISWI is Regulated by poly-ADP-ribosylation.
SALA, Anna;BURGIO, Giosalba;DI GESU', Dario;CORONA, Davide;
2008-01-01
Abstract
ATP-dependent nucleosome-remodeling enzymes and covalent modifiers of chromatin set the functional state of chromatin. However, how these enzymatic activities are coordinated in the nucleus is largely unknown. We found that the evolutionary conserved nucleosome-remodeling ATPase ISWI and the poly-ADP-ribose polymerase PARP genetically interact. We present evidence showing that ISWI is target of poly-ADP-ribosylation. Poly-ADP-ribosylation counteracts ISWI function in vitro and in vivo. Our work suggests that ISWI is a physiological target of PARP and that poly-ADP-ribosylation can be a new, important post-translational modification regulating the activity of ATP-dependent nucleosome remodelers.File | Dimensione | Formato | |
---|---|---|---|
file.pdf
accesso aperto
Tipologia:
Versione Editoriale
Dimensione
836.04 kB
Formato
Adobe PDF
|
836.04 kB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.