Pt-ttpy, a G-quadruplex binding platinum complex, induces telomere dysfunction and G-rich regions DNA damage

Author:

Ali Samar1,Lombardi Emilia Puig2ORCID,Ghosh Deepanjan34,Jia Tao34ORCID,Vitry Géraldine1,Saker Lina1,Poupon Joël5,Teulade-Fichou Marie-Paule34ORCID,Nicolas Alain2ORCID,Londono-Vallejo Arturo2ORCID,Bombard Sophie34ORCID

Affiliation:

1. INSERM UMRS 1007, Université de Paris, 75006 Paris, France

2. Institut Curie, PSL Research University, CNRS UMR3244, Sorbonne Université, Telomeres and Cancer lab, 75005 Paris, France

3. Institut Curie, CNRS UMR9187-INSERMU1196, CMBC, 91405 Orsay, France

4. Institut Curie, CNRS UMR9187-INSERMU1196, Université Paris-Saclay, 91405 Orsay, France

5. Hôpital Lariboisière, Laboratoire de Toxicologie Biologique, 2 rue Ambroise Paré, 75475 Paris, France

Abstract

Abstract Pt-ttpy (tolyl terpyridin-Pt complex) covalently binds to G-quadruplex (G4) structures in vitro and to telomeres in cellulo via its Pt moiety. Here, we identified its targets in the human genome, in comparison to Pt-tpy, its derivative without G4 affinity, and cisplatin. Pt-ttpy, but not Pt-tpy, induces the release of the shelterin protein TRF2 from telomeres concomitantly to the formation of DNA damage foci at telomeres but also at other chromosomal locations. γ-H2AX chromatin immunoprecipitation (ChIP-seq) after treatment with Pt-ttpy or cisplatin revealed accumulation in G- and A-rich tandemly repeated sequences, but not particularly in potential G4 forming sequences. Collectively, Pt-ttpy presents dual targeting efficiency on DNA, by inducing telomere dysfunction and genomic DNA damage at specific loci.

Funder

Centre National de la Recherche Scientifique

Horizon 2020 Framework Programme

Publisher

Oxford University Press (OUP)

Subject

Metals and Alloys,Biochemistry,Biomaterials,Biophysics,Chemistry (miscellaneous)

Reference94 articles.

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