The nucleosome: orchestrating DNA damage signaling and repair within chromatin

被引:24
作者
Agarwal, Poonam [1 ]
Miller, Kyle M. [1 ]
机构
[1] Univ Texas Austin, Inst Cellular & Mol Biol, Dept Mol Biosci, 2506 Speedway Stop A5000, Austin, TX 78712 USA
关键词
DNA double-strand break repair; DNA damage response; nucleosome acidic patch; chromatin; histone modifications; DOUBLE-STRAND BREAKS; PROMOTES HOMOLOGOUS RECOMBINATION; HISTONE H2AX; CRYSTAL-STRUCTURE; CORE PARTICLE; GENOMIC INSTABILITY; H4-K16; ACETYLATION; STRUCTURAL BASIS; REMOVES H2A.Z; PROTEIN;
D O I
10.1139/bcb-2016-0017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA damage occurs within the chromatin environment, which ultimately participates in regulating DNA damage response (DDR) pathways and repair of the lesion. DNA damage activates a cascade of signaling events that extensively modulates chromatin structure and organization to coordinate DDR factor recruitment to the break and repair, whilst also promoting the maintenance of normal chromatin functions within the damaged region. For example, DDR pathways must avoid conflicts between other DNA-based processes that function within the context of chromatin, including transcription and replication. The molecular mechanisms governing the recognition, target specificity, and recruitment of DDR factors and enzymes to the fundamental repeating unit of chromatin, i.e., the nucleosome, are poorly understood. Here we present our current view of how chromatin recognition by DDR factors is achieved at the level of the nucleosome. Emerging evidence suggests that the nucleosome surface, including the nucleosome acidic patch, promotes the binding and activity of several DNA damage factors on chromatin. Thus, in addition to interactions with damaged DNA and histone modifications, nucleosome recognition by DDR factors plays a key role in orchestrating the requisite chromatin response to maintain both genome and epigenome integrity.
引用
收藏
页码:381 / 395
页数:15
相关论文
共 181 条
  • [51] 53BP1 is a reader of the DNA-damage-induced H2A Lys 15 ubiquitin mark
    Fradet-Turcotte, Amelie
    Canny, Marella D.
    Escribano-Diaz, Cristina
    Orthwein, Alexandre
    Leung, Charles C. Y.
    Huang, Hao
    Landry, Marie-Claude
    Kitevski-LeBlanc, Julianne
    Noordermeer, Sylvie M.
    Sicheri, Frank
    Durocher, Daniel
    [J]. NATURE, 2013, 499 (7456) : 50 - +
  • [52] Phosphorylation of histone H2AX and activation of Mre11, Rad50, and Nbs1 in response to replication-dependent DNA double-strand breaks induced by mammalian DNA topoisomerase I cleavage complexes
    Furuta, T
    Takemura, H
    Liao, ZY
    Aune, GJ
    Redon, C
    Sedelnikova, OA
    Pilch, DR
    Rogakou, EP
    Celeste, A
    Chen, HT
    Nussenzweig, A
    Aladjem, MI
    Bonner, WM
    Pommier, Y
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (22) : 20303 - 20312
  • [53] The many faces of chromatin remodeling: SWItching beyond transcription
    Fyodorov, DV
    Kadonaga, JT
    [J]. CELL, 2001, 106 (05) : 523 - 525
  • [54] RNF168 Promotes Noncanonical K27 Ubiquitination to Signal DNA Damage
    Gatti, Marco
    Pinato, Sabrina
    Maiolica, Alessio
    Rocchio, Francesca
    Prato, Maria Giulia
    Aebersold, Ruedi
    Penengo, Lorenza
    [J]. CELL REPORTS, 2015, 10 (02): : 226 - 238
  • [55] A novel ubiquitin mark at the N-terminal tail of histone H2As targeted by RNF168 ubiquitin ligase
    Gatti, Marco
    Pinato, Sabrina
    Maspero, Elena
    Soffientini, Paolo
    Polo, Simona
    Penengo, Lorenza
    [J]. CELL CYCLE, 2012, 11 (13) : 2538 - 2544
  • [56] BMI1 Is Recruited to DNA Breaks and Contributes to DNA Damage-Induced H2A Ubiquitination and Repair
    Ginjala, Vasudeva
    Nacerddine, Karim
    Kulkarni, Atul
    Oza, Jay
    Hill, Sarah J.
    Yao, Ming
    Citterio, Elisabetta
    van Lohuizen, Maarten
    Ganesan, Shridar
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2011, 31 (10) : 1972 - 1982
  • [57] Recognizing and remodeling the nucleosome
    Glatt, Sebastian
    Alfieri, Claudio
    Mueller, Christoph W.
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 2011, 21 (03) : 335 - 341
  • [58] Featuring the nucleosome surface as a therapeutic target
    Gomes da Silva, Isabel Torres
    Lopes de Oliveira, Paulo Sergio
    Santos, Guilherme Martins
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2015, 36 (05) : 263 - 269
  • [59] Screen identifies bromodomain protein ZMYND8 in chromatin recognition of transcription-associated DNA damage that promotes homologous recombination
    Gong, Fade
    Chiu, Li-Ya
    Cox, Ben
    Aymard, Francois
    Clouaire, Thomas
    Leung, Justin W.
    Cammarata, Michael
    Perez, Mercedes
    Agarwal, Poonam
    Brodbelt, Jennifer S.
    Legube, Gaelle
    Miller, Kyle M.
    [J]. GENES & DEVELOPMENT, 2015, 29 (02) : 197 - 211
  • [60] Mammalian DNA repair: HATs and HDACs make their mark through histone acetylation
    Gong, Fade
    Miller, Kyle M.
    [J]. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2013, 750 (1-2) : 23 - 30