Poly(ADP-ribosyl)ation (PARylation) is involved in the maintenance of genomic methylation patterns through its control of DNA methyltranferase 1 (Dnmt1) activity. Our previous findings indicated that the CCCTC binding factor/Ctcf may be an important player in key events whereby PARylation controls the unmethylated status of some CpG-rich regions. Ctcf is able to activate Poly (ADP-ribose) polymerase 1 (Parp1) which ADP-ribosylates itself and, in turn, inhibits DNA methylation via non-covalent interaction between its ADP-ribose polymers and Dnmt1. By such a mechanism, Ctcf may preserve the epigenetic pattern at promoters of important housekeeping genes. Data here reported evidence Dnmt1 as a new protein partner of Ctcf. Moreover, we show that Ctcf forms a complex with Dnmt1 and PARylated Parp1 at specific Ctcf target sequences and that PARylation is responsible for the maintenance of the unmethylated status of some Ctcf-bound CpGs. We suggest a mechanism by which Parp1, tethered and activated at specific DNA target sites by Ctcf, preserves their methylation-free status.
Ctcf marks the CpGs that are maintained non methylated by PARP activity at Igf2/H19 locus / Zampieri, Michele; Guastafierro, Tiziana; Calabrese, Roberta; Ciccarone, Fabio; Bacalini, MARIA GIULIA; Reale, Anna; Perilli, M.; Passananti, C.; Caiafa, Paola. - (2010). (Intervento presentato al convegno PARP 2010 – 18th International Conference on ADP-ribose metabolism tenutosi a University of Zurich. Zurich, Switzerland nel 18-21 Agosto).
Ctcf marks the CpGs that are maintained non methylated by PARP activity at Igf2/H19 locus
ZAMPIERI, Michele;GUASTAFIERRO, Tiziana;CALABRESE, ROBERTA;CICCARONE, FABIO;BACALINI, MARIA GIULIA;REALE, Anna;CAIAFA, Paola
2010
Abstract
Poly(ADP-ribosyl)ation (PARylation) is involved in the maintenance of genomic methylation patterns through its control of DNA methyltranferase 1 (Dnmt1) activity. Our previous findings indicated that the CCCTC binding factor/Ctcf may be an important player in key events whereby PARylation controls the unmethylated status of some CpG-rich regions. Ctcf is able to activate Poly (ADP-ribose) polymerase 1 (Parp1) which ADP-ribosylates itself and, in turn, inhibits DNA methylation via non-covalent interaction between its ADP-ribose polymers and Dnmt1. By such a mechanism, Ctcf may preserve the epigenetic pattern at promoters of important housekeeping genes. Data here reported evidence Dnmt1 as a new protein partner of Ctcf. Moreover, we show that Ctcf forms a complex with Dnmt1 and PARylated Parp1 at specific Ctcf target sequences and that PARylation is responsible for the maintenance of the unmethylated status of some Ctcf-bound CpGs. We suggest a mechanism by which Parp1, tethered and activated at specific DNA target sites by Ctcf, preserves their methylation-free status.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
