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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Group name EquipeCTCS
Item Type Journal Article
Title A predictable conserved DNA base composition signature defines human core DNA replication origins
Creator Akerman et al.
Author Ildem Akerman
Author Bahar Kasaai
Author Alina Bazarova
Author Pau Biak Sang
Author Isabelle Peiffer
Author Marie Artufel
Author Romain Derelle
Author Gabrielle Smith
Author Marta Rodriguez-Martinez
Author Manuela Romano
Author Sandrina Kinet
Author Peter Tino
Author Charles Theillet
Author Naomi Taylor
Author Benoit Ballester
Author Marcel Méchali
Abstract DNA replication initiates from multiple genomic locations called replication origins. In metazoa, DNA sequence elements involved in origin specification remain elusive. Here, we examine pluripotent, primary, differentiating, and immortalized human cells, and demonstrate that a class of origins, termed core origins, is shared by different cell types and host ~80% of all DNA replication initiation events in any cell population. We detect a shared G-rich DNA sequence signature that coincides with most core origins in both human and mouse genomes. Transcription and G-rich elements can independently associate with replication origin activity. Computational algorithms show that core origins can be predicted, based solely on DNA sequence patterns but not on consensus motifs. Our results demonstrate that, despite an attributed stochasticity, core origins are chosen from a limited pool of genomic regions. Immortalization through oncogenic gene expression, but not normal cellular differentiation, results in increased stochastic firing from heterochromatin and decreased origin density at TAD borders.
Publication Nature Communications
Volume 11
Issue 1
Pages 4826
Date 2020-09-21
Journal Abbr Nat Commun
Language eng
DOI 10.1038/s41467-020-18527-0
ISSN 2041-1723
Library Catalog PubMed
Extra PMID: 32958757 PMCID: PMC7506530
Tags Animals, Base Composition, Base Sequence, Carcinogenesis, Cell Differentiation, Cells, Cultured, DNA, DNA Replication, Genome, Human, Heterochromatin, Humans, Mice, Nucleotide Motifs, original, Replication Origin, Transcription, Genetic
Date Added 2023/11/14 - 15:18:13
Date Modified 2023/11/14 - 15:46:18
Notes and Attachments PubMed entry (Attachment)
Texte intégral (Attachment)


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