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DNA damage and repair in the nucleosome: insights from computational methods

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  • معلومة اضافية
    • Contributors:
      Laboratoire de Chimie - UMR5182 (LC); École normale supérieure de Lyon (ENS de Lyon)-Université Claude Bernard Lyon 1 (UCBL); Université de Lyon-Université de Lyon-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS); Institut de Chimie de Nice (ICN); Université Nice Sophia Antipolis (1965 - 2019) (UNS)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UniCA); Laboratoire de Physique et Chimie Théoriques (LPCT); Institut de Chimie - CNRS Chimie (INC-CNRS)-Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS); ANR-20-CE29-0002,NucleoMAP,Simulations Multiéchelles de l'ADN Nucléosomal: Cartographier le Radical Cation Guanine(2020)
    • بيانات النشر:
      HAL CCSD
      Springer
    • الموضوع:
      2024
    • Collection:
      Université de Lyon: HAL
    • نبذة مختصرة :
      International audience ; Cellular DNA is constantly exposed to endogenous or exogenous factors that can induce lesions. Several types of lesions have been described that can result from UV/ionizing irradiations, oxidative stress or free radicals, among others. In order to overcome the deleterious effects of such damages, i.e. mutagenicity or cytotoxicity, cells possess a highly complex DNA repair machinery, involving repair enzymes targeting specific types of lesions through dedicated cellular pathways. In addition, DNA is highly compacted in the nucleus, the first level of compaction consisting of ~147 DNA base pairs wrapped around a core of histones, the so-called nucleosome core particle. In this complex environment, the DNA structure is highly constrained, and fine-tuned mechanisms involving remodeling processes are required to expose the DNA to repair enzymes and to facilitate the damage removal. However, these nucleosome-specific mechanisms remain poorly understood, and computational methods emerged only recently as powerful tools to investigate DNA damages in such complex systems as the nucleosome. In this mini-review, we summarize the latest advances brought out by computational approaches in the field, opening new exciting perspectives for the study of DNA damage and repair in the nucleosome context.
    • الرقم المعرف:
      10.1007/s12551-024-01183-9
    • الدخول الالكتروني :
      https://hal.science/hal-04743222
      https://hal.science/hal-04743222v1/document
      https://hal.science/hal-04743222v1/file/nucleosome_%20insights%20from%20computational%20methods_marked.pdf
      https://doi.org/10.1007/s12551-024-01183-9
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.D68B8189