Functional mapping of PHF6 complexes in chromatin remodeling, replication dynamics, and DNA repair

Author:

Alvarez Silvia1ORCID,da Silva Almeida Ana C.1,Albero Robert1ORCID,Biswas Mayukh1ORCID,Barreto-Galvez Angelica2ORCID,Gunning Thomas S.1ORCID,Shaikh Anam2,Aparicio Tomas1ORCID,Wendorff Agnieszka1,Piovan Erich34,Van Vlierberghe Pieter56,Gygi Steven7,Gautier Jean18ORCID,Madireddy Advaitha2ORCID,A. Ferrando Adolfo191011

Affiliation:

1. 1Institute for Cancer Genetics, Columbia University, New York, NY;

2. 2Rutgers Cancer Institute of New Jersey, New Brunswick, NJ;

3. 3UOC Immunologia e Diagnostica Molecolare Oncologica, Istituto Oncologico Veneto–Istituto Di Ricovero e Cura a Carattere Scientifico (IRCCS), Padova, Italy;

4. 4Dipartimento di Scienze Chirurgiche, Oncologiche e Gastroenterologiche, Sezione di Oncologia, Università di Padova, Padova, Italy;

5. 5Department of Biomolecular Medicine, Ghent University, Ghent, Belgium;

6. 6Cancer Research Institute Ghent, Ghent, Belgium;

7. 7Department of Cell Biology, Harvard Medical School, Boston, MA;

8. 8Department of Genetics and Development, College of Physicians and Surgeons, and

9. 9Department of Systems Biology, Columbia University, New York, NY; and

10. 10Department of Pediatrics and

11. 11Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY

Abstract

Abstract The Plant Homeodomain 6 gene (PHF6) encodes a nucleolar and chromatin-associated leukemia tumor suppressor with proposed roles in transcription regulation. However, specific molecular mechanisms controlled by PHF6 remain rudimentarily understood. Here we show that PHF6 engages multiple nucleosome remodeling protein complexes, including nucleosome remodeling and deacetylase, SWI/SNF and ISWI factors, the replication machinery and DNA repair proteins. Moreover, after DNA damage, PHF6 localizes to sites of DNA injury, and its loss impairs the resolution of DNA breaks, with consequent accumulation of single- and double-strand DNA lesions. Native chromatin immunoprecipitation sequencing analyses show that PHF6 specifically associates with difficult-to-replicate heterochromatin at satellite DNA regions enriched in histone H3 lysine 9 trimethyl marks, and single-molecule locus-specific analyses identify PHF6 as an important regulator of genomic stability at fragile sites. These results extend our understanding of the molecular mechanisms controlling hematopoietic stem cell homeostasis and leukemia transformation by placing PHF6 at the crossroads of chromatin remodeling, replicative fork dynamics, and DNA repair.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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