Error-Prone Replication through UV Lesions by DNA Polymerase θ Protects against Skin Cancers

被引:86
|
作者
Yoon, Jung-Hoon [1 ]
McArthur, Mark J. [2 ]
Park, Jeseong [1 ]
Basu, Debashree [1 ]
Wakamiya, Maki [1 ]
Prakash, Louise [1 ]
Prakash, Satya [1 ]
机构
[1] Univ Texas Med Branch, Dept Biochem & Mol Biol, 301 Univ Blvd, Galveston, TX 77555 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Vet Med & Surg, Houston, TX 77030 USA
关键词
POL-THETA; MUTATIONAL LANDSCAPE; GENOMIC INSTABILITY; PYRIMIDINE DIMERS; THYMINE GLYCOL; COMET ASSAY; P53; GENE; BYPASS; ETA; DAMAGE;
D O I
10.1016/j.cell.2019.01.023
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
Cancers from sun-exposed skin accumulate "driver'' mutations, causally implicated in oncogenesis. Because errors incorporated during translesion synthesis (TLS) opposite UV lesions would generate these mutations, TLS mechanisms are presumed to underlie cancer development. To address the role of TLS in skin cancer formation, we determined which DNA polymerase is responsible for generating UV mutations, analyzed the relative contributions of error-free TLS by Pol eta and error-prone TLS by Pol theta to the replication of UV-damaged DNA and to genome stability, and examined the incidence of UV-induced skin cancers in Pol theta(-/-), Pol eta(-/-), and Pol theta(-/-) Pol eta(-/-) mice. Our findings that the incidence of skin cancers rises in Pol theta(-/-) mice and is further exacerbated in Pol theta(-/-) Pol eta(-/-) mice compared with Pol eta(-/-) mice support the conclusion that error-prone TLS by Pol theta provides a safeguard against tumorigenesis and suggest that cancer formation can ensue in the absence of somatic point mutations.
引用
收藏
页码:1295 / +
页数:30
相关论文
共 50 条
  • [21] Error-prone DNA repair and translesion synthesis: Focus on the replication fork
    Bridges, BA
    DNA REPAIR, 2005, 4 (05) : 618 - 619
  • [22] ERROR-PRONE DNA-REPAIR AND REPLICATION IN RELATION TO MALIGNANT TRANSFORMATION
    TROSKO, JE
    CHANG, CC
    TRANSPLANTATION PROCEEDINGS, 1984, 16 (02) : 363 - 365
  • [23] Molecular insights into error-prone DNA replication and error-free lesion bypass
    Marx, A
    Summerer, D
    CHEMBIOCHEM, 2002, 3 (05) : 405 - 407
  • [24] Error-free and error-prone lesion bypass by human DNA polymerase κ in vitro
    Zhang, YB
    Yuan, FH
    Wu, XH
    Wang, M
    Rechkoblit, O
    Taylor, JS
    Geacintov, NE
    Wang, ZG
    NUCLEIC ACIDS RESEARCH, 2000, 28 (21) : 4138 - 4146
  • [25] Structural Dynamics as a Contributor to Error-prone Replication by an RNA-dependent RNA Polymerase
    Moustafa, Ibrahim M.
    Korboukh, Victoria K.
    Arnold, Jamie J.
    Smidansky, Eric D.
    Marcotte, Laura L.
    Gohara, David W.
    Yang, Xiaorong
    Antonieta Sanchez-Farran, Maria
    Filman, David
    Maranas, Janna K.
    Boehr, David D.
    Hogle, James M.
    Colina, Coray M.
    Cameron, Craig E.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (52) : 36229 - 36248
  • [26] Error-Prone DNA Polymerase IV preserves the memory of its interaction with RecA
    Tashjian, Tommy F.
    Lin, Ida
    Nguyen, Brian H.
    Godoy, Veronica G.
    FASEB JOURNAL, 2018, 32 (01):
  • [27] Construction of a highly error-prone DNA polymerase for developing organelle mutation systems
    Ji, Junwei
    Day, Anil
    NUCLEIC ACIDS RESEARCH, 2020, 48 (21) : 11868 - 11879
  • [28] Human breast cancer cells contain an error-prone DNA replication apparatus
    Sekowski, JW
    Malkas, LH
    Schnaper, L
    Bechtel, PE
    Long, BJ
    Hickey, RJ
    CANCER RESEARCH, 1998, 58 (15) : 3259 - 3263
  • [29] Crystal structure of a Y-family DNA polymerase in action: A mechanism for error-prone and lesion-bypass replication
    Ling, H
    Boudsocq, F
    Woodgate, R
    Yang, W
    CELL, 2001, 107 (01) : 91 - 102
  • [30] Does the Error-Prone DNA Polymerase eta Replicate Pyrimidine Dimers Correctly?
    Menck, Carlos F. M.
    ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2022, 63 : 34 - 35