Excision Repair in Mammalian Cells (*)

There are two types of structural anomalies that lead to mutation, a permanent change in DNA sequence. The first class involves normal bases in abnormal sequence context (mismatch, bulge, loop). The second class, which is referred to as DNA damage or DNA lesion, involves abnormal nucleotides (modified, fragmented, cross-linked) in normal sequence context. DNA lesions, in addition to causing mutations, also constitute replication and transcription blocks. Both types of structural anomalies are rectified by a series of enzymatic reactions referred to by the general term DNA repair (1-5). The repair reactions employed for correcting mismatches and lesions are similar in principle. The incorrect or damaged base is removed either as a base (base excision) or as an (oligo)nucleotide (nucleotide excision), the single-stranded gap resulting from the excision reaction is filled in by a polymerase (repair synthesis), and the newly synthesized DNA is ligated. Hence, there are two basic assays for measuring repair (6): the "incision/excision assay" and the "repair synthesis assay."

[1]  L. Pearl,et al.  The structural basis of specific base-excision repair by uracil–DNA glycosylase , 1996, Nature.

[2]  A. Sancar,et al.  Human DNA Repair Excision Nuclease , 1995, The Journal of Biological Chemistry.

[3]  J. Hurwitz,et al.  Phosphorylated and unphosphorylated forms of human single-stranded DNA-binding protein are equally active in simian virus 40 DNA replication and in nucleotide excision repair. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[4]  D. S. Hsu,et al.  Structure and Function of the UvrB Protein (*) , 1995, The Journal of Biological Chemistry.

[5]  C. Ingles,et al.  RPA involvement in the damage-recognition and incision steps of nucleotide excision repair , 1995, Nature.

[6]  M. Budd,et al.  DNA polymerases required for repair of UV-induced damage in Saccharomyces cerevisiae , 1995, Molecular and cellular biology.

[7]  R. Wood,et al.  Mammalian DNA nucleotide excision repair reconstituted with purified protein components , 1995, Cell.

[8]  John A. Tainer,et al.  Structure and function of the multifunctional DNA-repair enzyme exonuclease III , 1995, Nature.

[9]  D. Reinberg,et al.  Cdk-activating kinase complex is a component of human transcription factor TFIIH , 1995, Nature.

[10]  A. Sancar,et al.  The General Transcription-Repair Factor TFIIH Is Recruited to the Excision Repair Complex by the XPA Protein Independent of the TFIIE Transcription Factor (*) , 1995, The Journal of Biological Chemistry.

[11]  P. Hanawalt,et al.  Preferential repair of the transcribed DNA strand in the dihydrofolate reductase gene throughout the cell cycle in UV-irradiated human cells. , 1995, Mutation research.

[12]  D. S. Hsu,et al.  Reconstitution of Human DNA Repair Excision Nuclease in a Highly Defined System (*) , 1995, The Journal of Biological Chemistry.

[13]  Samuel H. Wilson,et al.  DNA Polymerase Conducts the Gap-filling Step in Uracil-initiated Base Excision Repair in a Bovine Testis Nuclear Extract (*) , 1995, The Journal of Biological Chemistry.

[14]  A. Sancar DNA repair in humans. , 1995, Annual review of genetics.

[15]  A. Sancar Mechanisms of DNA excision repair. , 1994, Science.

[16]  P. Modrich,et al.  Mismatch repair, genetic stability, and cancer. , 1994, Science.

[17]  P. Hanawalt Transcription-coupled repair and human disease. , 1994, Science.

[18]  P. Sung,et al.  A conserved 5' to 3' exonuclease activity in the yeast and human nucleotide excision repair proteins RAD2 and XPG. , 1994, The Journal of biological chemistry.

[19]  J. Hoeijmakers,et al.  The MO15 cell cycle kinase is associated with the TFIIH transcription-DNA repair factor , 1994, Cell.

[20]  D. S. Hsu,et al.  Substrate spectrum of human excinuclease: repair of abasic sites, methylated bases, mismatches, and bulky adducts. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[21]  P. O'Connor,et al.  Interaction of the p53-regulated protein Gadd45 with proliferating cell nuclear antigen. , 1994, Science.

[22]  A. Sancar,et al.  Human and E.coli excinucleases are affected differently by the sequence context of acetylaminofluorene-guanine adduct. , 1994, Nucleic acids research.

[23]  D. Reinberg,et al.  The multifunctional TFIIH complex and transcriptional control. , 1994, Trends in biochemical sciences.

[24]  S. Lippard,et al.  HMG-domain proteins specifically inhibit the repair of the major DNA adduct of the anticancer drug cisplatin by human excision nuclease. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[25]  G. Hannon,et al.  Differential effects by the p21 CDK inhibitor on PCNA-dependent DNA replication and repair , 1994, Nature.

[26]  M. Wold,et al.  Replication protein A mutants lacking phosphorylation sites for p34cdc2 kinase support DNA replication. , 1994, The Journal of biological chemistry.

[27]  P. Hanawalt,et al.  Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[28]  P. Sung,et al.  Human xeroderma pigmentosum group G gene encodes a DNA endonuclease. , 1994, Nucleic acids research.

[29]  A. Sancar,et al.  Determination of minimum substrate size for human excinuclease. , 1994, The Journal of biological chemistry.

[30]  K. Ishizaki,et al.  Increased UV‐induced SCEs but normal repair of DNA damage in p53‐deficient mouse cells , 1994, International journal of cancer.

[31]  R. Wood,et al.  Isolation of active recombinant XPG protein, a human DNA repair endonuclease. , 1994, The Journal of biological chemistry.

[32]  S. Elledge,et al.  Specific association between the human DNA repair proteins XPA and ERCC1. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[33]  A. Sancar,et al.  Formation of a ternary complex by human XPA, ERCC1, and ERCC4(XPF) excision repair proteins. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[34]  M. Y. Lee,et al.  DNA polymerase delta is involved in the cellular response to UV damage in human cells. , 1994, The Journal of biological chemistry.

[35]  J. Hoeijmakers,et al.  The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor. , 1994, The EMBO journal.

[36]  M. P. Carty,et al.  UV light‐induced DNA synthesis arrest in HeLa cells is associated with changes in phosphorylation of human single‐stranded DNA‐binding protein. , 1994, The EMBO journal.

[37]  D. Reinberg,et al.  Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II , 1994, Nature.

[38]  K. Tanaka,et al.  Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23. , 1994, The EMBO journal.

[39]  C. Harris,et al.  Hepatitis B virus X protein inhibits p53 sequence-specific DNA binding, transcriptional activity, and association with transcription factor ERCC3. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[40]  G. Chu,et al.  Cellular responses to cisplatin. The roles of DNA-binding proteins and DNA repair. , 1994, The Journal of biological chemistry.

[41]  B Demple,et al.  Repair of oxidative damage to DNA: enzymology and biology. , 1994, Annual review of biochemistry.

[42]  V. F. Liu,et al.  The ionizing radiation-induced replication protein A phosphorylation response differs between ataxia telangiectasia and normal human cells , 1993, Molecular and cellular biology.

[43]  S. Keeney,et al.  Comparative analysis of binding of human damaged DNA-binding protein (XPE) and Escherichia coli damage recognition protein (UvrA) to the major ultraviolet photoproducts: T[c,s]T, T[t,s]T, T[6-4]T, and T[Dewar]T. , 1993, The Journal of biological chemistry.

[44]  E. Winchester,et al.  Inhibition of DNA replication factor RPA by p53 , 1993, Nature.

[45]  P. Chambon,et al.  DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor. , 1993, Science.

[46]  A. Sancar,et al.  Molecular mechanism of transcription-repair coupling. , 1993, Science.

[47]  J. Hearst,et al.  DNA repair by eukaryotic nucleotide excision nuclease. Removal of thymine dimer and psoralen monoadduct by HeLa cell-free extract and of thymine dimer by Xenopus laevis oocytes. , 1993, The Journal of biological chemistry.

[48]  L. Thompson,et al.  Excision repair in man and the molecular basis of xeroderma pigmentosum syndrome. , 1993, Cold Spring Harbor symposia on quantitative biology.

[49]  P. Sung,et al.  DNA repair genes and proteins of Saccharomyces cerevisiae. , 1993, Annual review of genetics.

[50]  A. Collins,et al.  Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics. , 1993, Mutation research.

[51]  A. Sancar,et al.  Purification of PCNA as a nucleotide excision repair protein. , 1992, Nucleic Acids Research.

[52]  R. Wood,et al.  Proliferating cell nuclear antigen is required for DNA excision repair , 1992, Cell.

[53]  A. Sancar,et al.  Human nucleotide excision nuclease removes thymine dimers from DNA by incising the 22nd phosphodiester bond 5' and the 6th phosphodiester bond 3' to the photodimer. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[54]  S. Lippard,et al.  Specific binding of chromosomal protein HMG1 to DNA damaged by the anticancer drug cisplatin. , 1992, Science.

[55]  D. Housman,et al.  Isolation and characterization of human cDNA clones encoding a high mobility group box protein that recognizes structural distortions to DNA caused by binding of the anticancer agent cisplatin. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[56]  S. Keeney,et al.  Biochemical heterogeneity in xeroderma pigmentosum complementation group E. , 1992, Mutation research.

[57]  A. Fornace Mammalian genes induced by radiation; activation of genes associated with growth control. , 1992, Annual review of genetics.

[58]  T. Lindahl,et al.  Complementation of DNA repair in xeroderma pigmentosum group A cell extracts by a protein with affinity for damaged DNA. , 1991, The EMBO journal.

[59]  Y. Fujiwara,et al.  UV damage-specific DNA-binding protein in xeroderma pigmentosum complementation group E. , 1991, Biochemical and biophysical research communications.

[60]  D. Lane,et al.  Requirement for the replication protein SSB in human DMA excision repair , 1991, Nature.

[61]  A. Kwong,et al.  The in vitro replication of DNA containing the SV40 origin. , 1990, The Journal of biological chemistry.

[62]  L. Mullenders,et al.  The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[63]  W. Kaufmann,et al.  Defective postreplication repair in xeroderma pigmentosum variant fibroblasts. , 1990, Cancer research.

[64]  K. Brookman,et al.  Genetic diversity of UV-sensitive DNA repair mutants of Chinese hamster ovary cells. , 1981, Proceedings of the National Academy of Sciences of the United States of America.