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Written by research experts, this volume of Progress in Molecular Biology and Translational Science focuses on current science surrounding the mechanisms of DNA repair.… Read more
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Immediately download your ebook while waiting for your print delivery. No promo code needed.
Written by research experts, this volume of Progress in Molecular Biology and Translational Science focuses on current science surrounding the mechanisms of DNA repair.
Contributors
Preface
Chapter 1 Dynamics of Lesion Processing by Bacterial Nucleotide Excision Repair Proteins
I. Structural Insights of Bacterial Nucleotide Excision Repair
II. So Few DNA Repair Proteins, So Much DNA: Defining the Big Problem
III. Damage Searching by UvrA2 and UvrA2B2
IV. Future Directions
Chapter 2 Transcription-Coupled DNA Repair in Prokaryotes
I. Introduction
II. Background: Genomic Heterogeneity in NER and the Discovery of TCR
III. The Role of RNA Polymerase in TCR
IV. The Role of Mfd in TCR
V. The Role of UvrA in TCR
VI. The Role of UvrB in TCR
VII. Other Examples of Transcription-Related DNA Damage Processing in Bacteria
VIII. Conclusions
Chapter 3 The Functions of MutL in Mismatch Repair
I. Overview of DNA Mismatch Repair
II. MutL is a Multidomain Protein
III. Architecture of the Endonuclease Domain
IV. Regulation of the Endonuclease Activity of MutL
V. Concluding Remarks
Chapter 4 The Fpg/Nei Family of DNA Glycosylases
I. Introduction
II. Fpg/Nei Phylogeny
III. Fpg/Nei Structures
IV. Glycosylases Search for Lesions
V. Concluding Remarks
Chapter 5 Regulation of Base Excision Repair in Eukaryotes by Dynamic Localization Strategies
I. Base Excision Repair
II. Dynamic Localization of BER Proteins
III. Hypotheses on the Orchestration of Dynamic Localization
Chapter 6 Oxidized Base Damage and Single-Strand Break Repair in Mammalian Genomes
I. Oxidative DNA Damage and Its Repair in Mammalian Cells
II. Complexity and Sub-pathways of BER/SSBR
III. Nonconserved Terminal Extensions in Mammalian Early BER Proteins
IV. Posttranslational Modifications in Early BER Proteins
V. BER/SSBR Deficiency in Human Diseases
VI. Conclusions and Future Perspectives
Chapter 7 Homologous Recombination in Eukaryotes
I. Meiosis
II. DSB Repair in Somatic Cells
III. RAD52 Epistasis Group
IV. Recombination Mediators
V. RAD51 Paralogs
VI. DSB Repair in Chromatin
VII. Postsynaptic Removal of RAD51
VIII. Second-End Capture
IX. dHJ Dissolution
X. Holliday Junction Resolution
XI. Homeologous Recombination: The Interplay Between Mismatch Repair and HR
XII. Conclusion
Chapter 8 Overview for the Histone Codes for DNA Repair
I. Histone Modifications of Homologous Recombination Repair
II. Histone Modifications of NHEJ
III. Histone Modifications of Nucleotide Excision Repair
IV. Histone Modifications of Base Excision Repair
V. DNA Mismatch Repair and Histone Modifications
Chapter 9 The RSC and INO80 Chromatin-Remodeling Complexes in DNA Double-Strand Break Repair
I. Introduction
II. RSC
III. INO80
IV. Perspectives
Chapter 10 Mechanistic Links Between ATM and Histone Methylation Codes During DNA Repair
I. The DNA Damage Response
II. Ataxia telangiectasia and the ATM Kinase
III. The Tip60 Acetyltransferase
IV. H3K9me3 and DDR
V. Conclusions and Implications for Cancer Therapy
Chapter 11 Exploiting Synthetic Lethal Interactions Between DNA Damage Signaling, Checkpoint Control, and p53 for Targeted Cancer Therapy
I. Introduction
II. The Concept of Synthetic Lethality in Cancer Therapy
III. Synthetic Lethality Between PARP1 and BRCA1/2 as a Model for Enhancing DNA Damage-Induced Cell Death
IV. Synthetic Lethality in the Context of p53 Mutations
V. Potential for Future Therapies
Index