Proteomic characterization of chromosomal common fragile site (CFS)-associated proteins uncovers ATRX as a regulator of CFS stability

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Standard

Proteomic characterization of chromosomal common fragile site (CFS)-associated proteins uncovers ATRX as a regulator of CFS stability. / Pladevall-Morera, David; Munk, Stephanie; Ingham, Andreas; Garribba, Lorenza; Albers, Eliene; Liu, Ying; Olsen, Jesper V.; Lopez-Contreras, Andres J.

In: Nucleic Acids Research, Vol. 47, No. 15, 2019, p. 8004-8018.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Pladevall-Morera, D, Munk, S, Ingham, A, Garribba, L, Albers, E, Liu, Y, Olsen, JV & Lopez-Contreras, AJ 2019, 'Proteomic characterization of chromosomal common fragile site (CFS)-associated proteins uncovers ATRX as a regulator of CFS stability', Nucleic Acids Research, vol. 47, no. 15, pp. 8004-8018. https://doi.org/10.1093/nar/gkz510

APA

Pladevall-Morera, D., Munk, S., Ingham, A., Garribba, L., Albers, E., Liu, Y., Olsen, J. V., & Lopez-Contreras, A. J. (2019). Proteomic characterization of chromosomal common fragile site (CFS)-associated proteins uncovers ATRX as a regulator of CFS stability. Nucleic Acids Research, 47(15), 8004-8018. https://doi.org/10.1093/nar/gkz510

Vancouver

Pladevall-Morera D, Munk S, Ingham A, Garribba L, Albers E, Liu Y et al. Proteomic characterization of chromosomal common fragile site (CFS)-associated proteins uncovers ATRX as a regulator of CFS stability. Nucleic Acids Research. 2019;47(15):8004-8018. https://doi.org/10.1093/nar/gkz510

Author

Pladevall-Morera, David ; Munk, Stephanie ; Ingham, Andreas ; Garribba, Lorenza ; Albers, Eliene ; Liu, Ying ; Olsen, Jesper V. ; Lopez-Contreras, Andres J. / Proteomic characterization of chromosomal common fragile site (CFS)-associated proteins uncovers ATRX as a regulator of CFS stability. In: Nucleic Acids Research. 2019 ; Vol. 47, No. 15. pp. 8004-8018.

Bibtex

@article{c41ce5075fd8405693d966e2ee174866,
title = "Proteomic characterization of chromosomal common fragile site (CFS)-associated proteins uncovers ATRX as a regulator of CFS stability",
abstract = "Common fragile sites (CFSs) are conserved genomic regions prone to break under conditions of replication stress (RS). Thus, CFSs are hotspots for rearrangements in cancer and contribute to its chromosomal instability. Here, we have performed a global analysis of proteins that recruit to CFSs upon mild RS to identify novel players in CFS stability. To this end, we performed Chromatin Immunoprecipitation (ChIP) of FANCD2, a protein that localizes specifically to CFSs in G2/M, coupled to mass spectrometry to acquire a CFS interactome. Our strategy was validated by the enrichment of many known regulators of CFS maintenance, including Fanconi Anemia, DNA repair and replication proteins. Among the proteins identified with unknown functions at CFSs was the chromatin remodeler ATRX. Here we demonstrate that ATRX forms foci at a fraction of CFSs upon RS, and that ATRX depletion increases the occurrence of chromosomal breaks, a phenotype further exacerbated under mild RS conditions. Accordingly, ATRX depletion increases the number of 53BP1 bodies and micronuclei, overall indicating that ATRX is required for CFS stability. Overall, our study provides the first proteomic characterization of CFSs as a valuable resource for the identification of novel regulators of CFS stability.",
author = "David Pladevall-Morera and Stephanie Munk and Andreas Ingham and Lorenza Garribba and Eliene Albers and Ying Liu and Olsen, {Jesper V.} and Lopez-Contreras, {Andres J.}",
note = "Corrigendum. This is a correction to: Nucleic Acids Research, Volume 47, Issue 15, 05 September 2019, Pages 8004–8018. https://doi.org/10.1093/nar/gkz591",
year = "2019",
doi = "10.1093/nar/gkz510",
language = "English",
volume = "47",
pages = "8004--8018",
journal = "Nucleic Acids Research",
issn = "0305-1048",
publisher = "Oxford University Press",
number = "15",

}

RIS

TY - JOUR

T1 - Proteomic characterization of chromosomal common fragile site (CFS)-associated proteins uncovers ATRX as a regulator of CFS stability

AU - Pladevall-Morera, David

AU - Munk, Stephanie

AU - Ingham, Andreas

AU - Garribba, Lorenza

AU - Albers, Eliene

AU - Liu, Ying

AU - Olsen, Jesper V.

AU - Lopez-Contreras, Andres J.

N1 - Corrigendum. This is a correction to: Nucleic Acids Research, Volume 47, Issue 15, 05 September 2019, Pages 8004–8018. https://doi.org/10.1093/nar/gkz591

PY - 2019

Y1 - 2019

N2 - Common fragile sites (CFSs) are conserved genomic regions prone to break under conditions of replication stress (RS). Thus, CFSs are hotspots for rearrangements in cancer and contribute to its chromosomal instability. Here, we have performed a global analysis of proteins that recruit to CFSs upon mild RS to identify novel players in CFS stability. To this end, we performed Chromatin Immunoprecipitation (ChIP) of FANCD2, a protein that localizes specifically to CFSs in G2/M, coupled to mass spectrometry to acquire a CFS interactome. Our strategy was validated by the enrichment of many known regulators of CFS maintenance, including Fanconi Anemia, DNA repair and replication proteins. Among the proteins identified with unknown functions at CFSs was the chromatin remodeler ATRX. Here we demonstrate that ATRX forms foci at a fraction of CFSs upon RS, and that ATRX depletion increases the occurrence of chromosomal breaks, a phenotype further exacerbated under mild RS conditions. Accordingly, ATRX depletion increases the number of 53BP1 bodies and micronuclei, overall indicating that ATRX is required for CFS stability. Overall, our study provides the first proteomic characterization of CFSs as a valuable resource for the identification of novel regulators of CFS stability.

AB - Common fragile sites (CFSs) are conserved genomic regions prone to break under conditions of replication stress (RS). Thus, CFSs are hotspots for rearrangements in cancer and contribute to its chromosomal instability. Here, we have performed a global analysis of proteins that recruit to CFSs upon mild RS to identify novel players in CFS stability. To this end, we performed Chromatin Immunoprecipitation (ChIP) of FANCD2, a protein that localizes specifically to CFSs in G2/M, coupled to mass spectrometry to acquire a CFS interactome. Our strategy was validated by the enrichment of many known regulators of CFS maintenance, including Fanconi Anemia, DNA repair and replication proteins. Among the proteins identified with unknown functions at CFSs was the chromatin remodeler ATRX. Here we demonstrate that ATRX forms foci at a fraction of CFSs upon RS, and that ATRX depletion increases the occurrence of chromosomal breaks, a phenotype further exacerbated under mild RS conditions. Accordingly, ATRX depletion increases the number of 53BP1 bodies and micronuclei, overall indicating that ATRX is required for CFS stability. Overall, our study provides the first proteomic characterization of CFSs as a valuable resource for the identification of novel regulators of CFS stability.

U2 - 10.1093/nar/gkz510

DO - 10.1093/nar/gkz510

M3 - Journal article

C2 - 31180492

VL - 47

SP - 8004

EP - 8018

JO - Nucleic Acids Research

JF - Nucleic Acids Research

SN - 0305-1048

IS - 15

ER -

ID: 222691794