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Coline Arnould

Researcher at University of Toulouse

Publications -  11
Citations -  634

Coline Arnould is an academic researcher from University of Toulouse. The author has contributed to research in topics: Chromatin & Homologous recombination. The author has an hindex of 6, co-authored 9 publications receiving 375 citations. Previous affiliations of Coline Arnould include Centre national de la recherche scientifique.

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Comprehensive Mapping of Histone Modifications at DNA Double-Strand Breaks Deciphers Repair Pathway Chromatin Signatures

TL;DR: This study revealed the existence of a DSB-induced monoubiquitination-to-acetylation switch on histone H2B lysine 120, likely mediated by the SAGA complex, as well as higher-order signaling at HR-repaired DSBs whereby hist one H1 is evicted while ubiquitin and 53BP1 accumulate over the entire γH2AX domains.
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Genome-wide mapping of long-range contacts unveils clustering of DNA double-strand breaks at damaged active genes

TL;DR: Investigation of clustering of DNA double-strand breaks in mammalian cells reveals that, when damaged, active genes, compared with the rest of the genome, exhibit a distinctive behavior, remaining largely unrepaired and clustered in G1, and being repaired via homologous recombination in postreplicative cells.
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Loop extrusion as a mechanism for formation of DNA damage repair foci

TL;DR: In this article, the authors show that topologically associating domains are functional units of the DNA damage response, and are instrumental for the correct establishment of γH2AX-53BP1 chromatin domains in a manner that involves one-sided cohesin-mediated loop extrusion on both sides of the DSB.
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A cohesin/HUSH- and LINC-dependent pathway controls ribosomal DNA double-strand break repair

TL;DR: The data indicate that rDNA break localization at the nucleolar periphery is not a direct consequence of transcriptional repression but rather is an active process that shares features with the mobilization of persistent DSB in active genes and heterochromatin.
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The Secret Life of Chromosome Loops upon DNA Double-Strand Break

TL;DR: The influence of initial and DSB-induced chromatin conformation and the strong potential of 3C-based technologies to decipher the contribution of chromosome architecture during DSB repair are discussed.