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Nausica Arnoult

Researcher at Salk Institute for Biological Studies

Publications -  22
Citations -  1825

Nausica Arnoult is an academic researcher from Salk Institute for Biological Studies. The author has contributed to research in topics: Telomere & Heterochromatin. The author has an hindex of 15, co-authored 19 publications receiving 1579 citations. Previous affiliations of Nausica Arnoult include University of Colorado Boulder & Catholic University of Leuven.

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Telomere length regulates TERRA levels through increased trimethylation of telomeric H3K9 and HP1α

TL;DR: Using cell lines of various origins, it is shown that telomere elongation consistently represses TERRA expression, and supports the existence of a negative-feedback mechanism in which longer TERRA moleculesRepression is mediated by increased trimethylated H3K9 density at telomeres and by heterochromatin protein HP1α, restricting human TPE to telomerre transcription.
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Replication fork movement sets chromatin loop size and origin choice in mammalian cells

TL;DR: It is found that slowing the replication speed triggers the recruitment of latent origins within minutes, allowing the completion of S phase in a timely fashion, suggesting a mechanism of origin programming in which replication speed determines the spacing of anchorage regions of chromatin loops, that, in turn, controls the choice of initiation sites.
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Rapid induction of alternative lengthening of telomeres by depletion of the histone chaperone ASF1

TL;DR: The induction of ALT phenotypes as a consequence of ASF1 depletion strongly supports the hypothesis that ALT is a result of histone management dysfunction.
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Regulation of DNA repair pathway choice in S and G2 phases by the NHEJ inhibitor CYREN

TL;DR: It is proposed that CYREN is a direct cell-cycle-dependent inhibitor of cNHEJ that promotes error-free repair by homologous recombination during cell cycle phases when sister chromatids are present.
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Complex interactions between the DNA-damage response and mammalian telomeres

TL;DR: This work focuses on mammalian telomeres and summarizes and interpret recent discoveries in detail, focusing on how repair pathways are inhibited, how resection and replication are controlled and how these mechanisms govern cell fate during senescence, crisis and transformation.