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Nucleotide excision repair

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types. The XPC gene is responsible for a protein which recognizes DNA during the early portion of the NER pathway. This gene can have polymorphisms at Intron 9 and SNPs in Exon 15 which have been correlated with cancer risk as well. Research has shown that a biallelic poly (AT) insertion/deletion polymorphism in Intron 9 of XPC is associated with increased risk for skin, breast and prostate cancers, especially in North Indian populations.
3054: 220:) can also recognize some types of damage caused by UV light. Additionally, XPA performs a function in damage recognition that is as yet poorly defined. Upon identification of a damaged site, subsequent repair proteins are then recruited to the damaged DNA to verify presence of DNA damage, excise the damaged DNA surrounding the lesion then fill in the repair patch. 509:. In a study relapse rates of high-risk stage II and III colorectal cancers, XPD (ERCC2) polymorphism 2251A>C was significantly correlated with early relapse after chemotherapeutic treatment. Studies have indicated that the effects of polymorphic NER genes is additive, with greater frequency of variants, greater cancer risk presents. 249:
At any given time, most of the genome in an organism is not undergoing transcription; there is a difference in NER efficiency between transcriptionally silent and transcriptionally active regions of the genome. For many types of lesions, NER repairs the transcribed strands of transcriptionally active
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Qiao Y, Spitz MR, Guo Z, Hadeyati M, Grossman L, Kraemer KH, Wei Q (November 2002). "Rapid assessment of repair of ultraviolet DNA damage with a modified host-cell reactivation assay using a luciferase reporter gene and correlation with polymorphisms of DNA repair genes in normal human lymphocytes".
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are the last two proteins associated with the main NER repair complex. These two proteins are present prior to TFIIH binding since they are involved with verifying DNA damage. They may also protect single-stranded DNA. After verification, the 5' side incision is made and DNA repair begins before the
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Eukaryotic nucleotide excision repair can be divided into two subpathways: global genomic NER (GG-NER) and transcription coupled NER (TC-NER). Three different sets of proteins are involved in recognizing DNA damage for each subpathway. After damage recognition, the three subpathways converge for the
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The study of a hereditary cancer, xeroderma pigmentosum has helped identify several genes which encode proteins in the NER pathway, two of which are XPC and XPD. XP is caused by a homozygous deficiency in UV DNA damage repair (GG-NER) which increases the patients' risk of skin cancer by 1000-fold.
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genes. XPD, also known as ERCC2, serves to open DNA around the site of damage during NER, in addition to other transcriptional activities. Studies have shown that polymorphisms at Exon 10 (G>A)(Asp312Asn) and Exon 23 (A>T)(Lys751Gln) are linked with genetic predisposition to several cancer
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4 nucleotides downstream of the DNA damage, and the UvrC cleaves a phosphodiester bond 8 nucleotides upstream of the DNA damage and created 12 nucleotide excised segment. DNA helicase II (sometimes called UvrD) then comes in and removes the excised segment by actively breaking the hydrogen bonds
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Vermeij WP, Dollé ME, Reiling E, Jaarsma D, Payan-Gomez C, Bombardieri CR, Wu H, Roks AJ, Botter SM, van der Eerden BC, Youssef SA, Kuiper RV, Nagarajah B, van Oostrom CT, Brandt RM, Barnhoorn S, Imholz S, Pennings JL, de Bruin A, Gyenis Á, Pothof J, Vijg J, van Steeg H, Hoeijmakers JH (2016).
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heterodimeric protein cuts on the 5' side. The dual incision leads to the removal of a ssDNA with a single strand gap of 25~30 nucleotides. The small, excised, damage-containing DNA (sedDNA) oligonucleotides are initially released from the duplex in complex with TFIIH but then dissociate in an
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that uses ATP hydrolysis to translocate on dsDNA upstream of the transcription bubble and forward translocate RNA polymerase, thus initiating dissociation of the RNA Polymerase ternary elongation complex. TRCF also recruits the Uvr(A)BC nucleotide excision repair machinery by direct physical
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Global genomic NER repairs damage in both transcribed and untranscribed DNA strands in active and inactive genes throughout the genome. This process is not dependent on transcription. This pathway employs several "damage sensing" proteins including the DNA-damage binding (DDB) and XPC-Rad23B
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As reviewed by Gorbunova et al., studies of NER in different cells and tissues from young and old individuals frequently have shown a decrease in NER capacity with increasing age. This decline may be due to reduced constitutive levels of proteins employed in the NER pathway.
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stalls at a lesion in DNA: the blocked RNA polymerase serves as a damage recognition signal, which replaces the need for the distortion recognition properties of the XPC-RAD23B and DDB complexes. CS proteins (CSA and CSB) bind some types of DNA damage instead of XPC-Rad23B.
99:. NER can be divided into two subpathways: global genomic NER (GG-NER or GGR) and transcription coupled NER (TC-NER or TCR). The two subpathways differ in how they recognize DNA damage but they share the same process for lesion incision, repair, and ligation. 253:
TC-NER and GG-NER differ only in the initial steps of DNA damage recognition. The principal difference between TC-NER and GG-NER is that TC-NER does not require XPC or DDB proteins for distortion recognition in mammalian cells. Instead TC-NER initiates when
699:(CSB) mutations. Mutations in the CSA gene account for about 20% of CS cases. Individuals with CSA and CSB are characterised by severe postnatal growth and mental retardation and accelerated aging leading to premature death at the age of 12 to 16 years. 478:
cases found modest association between NER specific SNP polymorphisms and lung cancer risk. The results indicate that some inherited polymorphic variations in NER genes may result in predisposition to lung cancer, and potentially other cancer states.
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capacity resulting in an increase likelihood of cancer development. While the functional impact of all polymorphisms has not been characterized, some polymorphisms in DNA repair genes or their regulatory sequences do induce
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Andressoo JO, Mitchell JR, de Wit J, Hoogstraten D, Volker M, Toussaint W, Speksnijder E, Beems RB, van Steeg H, Jans J, de Zeeuw CI, Jaspers NG, Raams A, Lehmann AR, Vermeulen W, Hoeijmakers JH, van der Horst GT (2006).
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between the complementary bases. The resultant gap is then filled in using DNA polymerase I and DNA ligase. The basic excision process is very similar in higher cells, but these cells usually involve many more proteins –
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Barnhoorn S, Uittenboogaard LM, Jaarsma D, Vermeij WP, Tresini M, Weymaere M, Menoni H, Brandt RM, de Waard MC, Botter SM, Sarker AH, Jaspers NG, van der Horst GT, Cooper PK, Hoeijmakers JH, van der Pluijm I (2014).
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TC-NER initiates when RNA polymerase stalls at a lesion in DNA, whereupon protein complexes help move the polymerase backwards. Mutations in TC-NER machinery are responsible for multiple genetic disorders including:
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Spitz MR, Wu X, Wang Y, Wang LE, Shete S, Amos CI, Guo Z, Lei L, Mohrenweiser H, Wei Q (February 2001). "Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients".
465:(SNPs) and nonsynonymous coding SNPs (nsSNPs) are present at very low levels (>1%) in the human population. If located in NER genes or regulatory sequences, such mutations can negatively affect 658:
with pronounced degenerative phenotypes in both liver and brain. These mutant mice develop a multi-system premature aging degenerative phenotype that appears to strengthen the link between
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ATP-dependent manner and become bound to replication protein A (RPA). Inhibition of gap filling DNA synthesis and ligation results in an accumulation of RPA-bound sedDNAs in the cell.
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Blankenburg S, König IR, Moessner R, Laspe P, Thoms KM, Krueger U, Khan SG, Westphal G, Berking C, Volkenandt M, Reich K, Neumann C, Ziegler A, Kraemer KH, Emmert S (June 2005).
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and 6,4-photoproducts. Recognition of the damage leads to removal of a short single-stranded DNA segment that contains the lesion. The undamaged single-stranded DNA remains and
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II (sometimes also known as UvrD in this complex). First, a UvrA-UvrB complex scans the DNA, with the UvrA subunit recognizing distortions in the helix, caused for example by
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In heterozygous patients, the risk of cancer is sporadic but can be predicted based on analytical assessment of polymorphisms in XP related DNA repair genes purified from
2233:"ERCC2 2251A>C genetic polymorphism was highly correlated with early relapse in high-risk stage II and stage III colorectal cancer patients: a preliminary study" 605:(XPD) mutant human and mouse show evidence of defective repair of oxidative DNA damages that may underlie the segmental progeroid (premature aging) symptoms (see 412:. When the complex recognizes such a distortion, the UvrA subunit leaves and an UvrC protein comes in and binds to the UvrB monomer and, hence, forms a new UvrBC 312:
act as a 5'-3' and 3'-5' helicase, respectively — they help unwind DNA and generate a junction between the double-stranded and single-stranded DNA around the
2421:"XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase" 386: 2939:"TFIIH-mediated nucleotide excision repair and initiation of mRNA transcription in an optimized cell-free DNA repair and RNA transcription assay" 2520:
Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH (2006).
134:, there are 9 major proteins involved in NER. Deficiencies in certain proteins leads to disease; protein names are associated with the disease. 2050:"Genetic variation in nucleotide excision repair pathway genes influence prostate and bladder cancer susceptibility in North Indian population" 357:(PCNA) onto the DNA strand. This allows DNA polymerases implicated in repair (ÎŽ, Δ and/or Îș) to copy the undamaged strand via translocation. 2471:"An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria" 3058: 457:
Though historical studies have shown inconsistent results, genetic variation or mutation to nucleotide excision repair genes can impact
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mutant mice show features of accelerated aging, and have a limited lifespan. Accelerated aging in the mutant involves numerous organs.
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Wang M, Gu D, Zhang Z, Zhou J, Zhang Z (2009). "XPD polymorphisms, cigarette smoking, and bladder cancer risk: a meta-analysis".
453:. Unrepaired damage or malfunctioning proteins associated with excision repair could lead to unregulated cell growth and cancer. 3425: 2140:
Shore RE, Zeleniuch-Jacquotte A, Currie D, Mohrenweiser H, Afanasyeva Y, Koenig KL, Arslan AA, Toniolo P, Wirgin I (May 2008).
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Truglio JJ, Croteau DL, Van Houten B, Kisker C (February 2006). "Prokaryotic nucleotide excision repair: the UvrABC system".
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Sakoda LC, Loomis MM, Doherty JA, Julianto L, Barnett MJ, Neuhouser ML, Thornquist MD, Weiss NS, Goodman GE, Chen C (2012).
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The importance of NER is evidenced by the severe human diseases that result from in-born genetic mutations of NER proteins.
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Xeroderma pigmentosum (XP): severe photosensitivity, high cancer rates in areas of the body exposed to the sun (e.g. skin)
3141: 2522:"Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome" 92: 3394: 3325: 2101:"Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: a case-control study" 354: 61: 3409: 659: 75:
Nucleotide excision repair (NER) is a particularly important excision mechanism that removes DNA damage induced by
2775:"Genome Instability in Development and Aging: Insights from Nucleotide Excision Repair in Humans, Mice, and Worms" 597:, retinal degeneration, white matter hypomethylation, central nervous system calcification, reduced stature, and 521:
in genes employed in NER cause features of premature aging. These genes and their corresponding proteins include
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Two important genes in the NER pathway for which polymorphism has shown functional and phenotypic impact are the
182:, and others also participate in nucleotide excision repair. A more complete list of proteins involved in NER is 462: 52:. Three excision repair pathways exist to repair single stranded DNA damage: Nucleotide excision repair (NER), 25:
Diagram of both the TC-NER and GG-NER pathways. The two pathways differ only in initial DNA damage recognition.
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Kwok PY, Gu Z (December 1999). "Single nucleotide polymorphism libraries: why and how are we building them?".
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A schematic representation of models for the nucleotide excision repair pathway controlled by Uvr proteins.
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Koch S, Garcia Gonzalez O, Assfalg R, Schelling A, SchÀfer P, Scharffetter-Kochanek K, Iben S (2014).
2626:"Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency" 1955:"The XPD variant alleles are associated with increased aromatic DNA adduct level and lung cancer risk" 1636:"True lies: the double life of the nucleotide excision repair factors in transcription and DNA repair" 1371: 297: 2275: 1592: 3308: 3230: 3079: 728: 1773:"Involvement of nucleotide excision and mismatch repair mechanisms in double strand break repair" 785: 3420: 3330: 3125: 3186: 1093:
Transcription elongation factor; involved in transcription coupling and chromatin remodelling
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Involved in incision on 5' side of damage; stabilizes TFIIH; structure specific endonuclease
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are first recruited to the site of DNA damage (XPG stabilizes TFIIH). The TFIIH subunits of
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3' side incision. This helps reduce exposed single stranded DNA during the repair process.
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Mutations in GG-NER machinery are responsible for multiple genetic disorders including:
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genes faster than it repairs nontranscribed strands and transcriptionally silent DNA.
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Hou SM, FĂ€lt S, Angelini S, Yang K, Nyberg F, Lambert B, Hemminki K (April 2002).
95:. Final ligation to complete NER and form a double stranded DNA is carried out by 3120: 3029: 2642: 2586: 2436: 1566: 2981:
Frit P, Kwon K, Coin F, Auriol J, Dubaele S, Salles B, Egly JM (December 2002).
631:(XPF) in humans results in a variety of conditions including accelerated aging. 216:-Rad23B complex is responsible for distortion recognition, while DDB1 and DDB2 ( 2380:"Nucleotide excision repair disorders and the balance between cancer and aging" 1788: 255: 241: 212:
complexes that constantly scan the genome and recognize helix distortions: the
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Ellenberger T, Friedberg EC, Walker GS, Wolfram S, Wood RJ, Schultz R (2006).
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Mellon I (September 2005). "Transcription-coupled repair: a complex affair".
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enzyme complex, which consists of four Uvr proteins: UvrA, UvrB, UvrC, and
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represent proteins linked to Cockayne syndrome. Additionally, the proteins
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Involved in incision on 3' side of damage; structure specific endonuclease
642:(XP) alone, or in combination with the severe neurodevelopmental disorder 2841: 2396: 2379: 722: 589:(TTD) or a combination of XP and TTD (XPTTD), or a combination of XP and 475: 131: 2791: 2343: 650:(XPG) mutant mouse model presents features of premature aging including 203: 3335: 3156: 3095: 2538: 2521: 1486: 994:
ATPase and helicase activity; transcription factor II H (TFIIH) subunit
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ATPase and helicase activity; transcription factor II H (TFIIH) subunit
695:(CSA) mutations generally give rise to a more moderate form of CS than 646:(CS) or the infantile lethal cerebro-oculo-facio-skeletal syndrome. An 506: 492: 466: 450: 217: 213: 147: 143: 127: 123: 119: 96: 80: 33: 2873:
Goukassian D, Gad F, Yaar M, Eller MS, Nehal US, Gilchrest BA (2000).
2497: 2158: 2142:"Polymorphisms in XPC and ERCC2 genes, smoking and breast cancer risk" 2141: 1749: 262:
Other repair mechanisms are possible but less accurate and efficient.
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Involved in incision on 3' side of damage; forms complex with XPF
817: 601:(loss of subcutaneous fat tissue). XPCS and TTD fibroblasts from 49: 3488: 3243: 3196: 3191: 3053: 1272: 1239: 663: 458: 433: 300:(TFIIH) is the key enzyme involved in dual excision. TFIIH and 179: 175: 1735: 64:
in DNA, it can correct only damaged bases that are removed by
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Huang MY, Fang WY, Lee SC, Cheng TL, Wang JY, Lin SR (2008).
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Ubiquitin ligase complex; interacts with CSB and p44 of TFIIH
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International Journal of Molecular Epidemiology and Genetics
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Carroll SB; Wessler SR; Griffiths AJFl; Lewontin RC (2008).
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changes and are involved in cancer development. A study of
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The process of nucleotide excision repair is controlled in
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Schematic depicts binding of proteins involved with TC-NER.
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Schematic depicts binding of proteins involved with GG-NER.
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TC-NER also exists in bacteria, and is mediated by the
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Interacts with XPD and XPB subunits of TFIIH helicases
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Journal of Toxicology and Environmental Health Part A
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Damage recognition; interacts with XPA, CSA, and CSB
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damage occurs constantly because of chemicals (e.g.
1952: 1854: 1685:Morita R, Nakane S, Shimada A, et al. (2010). 1684: 2980: 2519: 2378:Andressoo JO, Hoeijmakers JH, Mitchell JR (2006). 2038: 2983:"Transcriptional activators stimulate DNA repair" 2772: 2230: 1400:Involved in incision, forms complex around lesion 581:(XPD) gene can lead to various syndromes, either 316:. In addition to stabilizing TFIIH, XPG also has 3534: 2824:Gorbunova V, Seluanov A, Mao Z, Hine C (2007). 2618: 2616: 2614: 2569:Gregg SQ, Robinson AR, Niedernhofer LJ (2011). 2373: 2371: 2288: 1993: 449:DNA excision pathways work in tandem to repair 375: 1855:Karahalil B, Bohr V, Wilson D (October 2012). 1633: 1629: 1627: 1610:. New York: W.H. Freeman and Co. p. 534. 198: 190:steps of dual incision, repair, and ligation. 118:Nucleotide excision repair is more complex in 3080: 2977:Article on the relation between TFIIH and NER 2936: 2226: 2224: 499: 265: 223: 110:are two examples of NER associated diseases. 2866: 2817: 2766: 2717: 2668: 2611: 2562: 2513: 2461: 2412: 2368: 2310: 2282: 2187: 2185: 2133: 2092: 2047: 1987: 1946: 1770: 702: 284:(CS): photosensitivity, mental retardation, 91:uses it as a template to synthesize a short 2674: 1905: 1848: 1813: 1764: 1729: 1678: 1624: 1541: 864:Damage recognition; forms complex with DDB2 60:(MMR). While the BER pathway can recognize 3087: 3073: 2418: 2221: 1547: 1291:Damage recognition, forms complex with XPC 1258:Damage recognition; forms complex with XPC 833:Damage recognition; forms complex with XPC 483:NER dysfunction result of DNA polymorphism 2998: 2962: 2890: 2849: 2800: 2790: 2749: 2700: 2651: 2641: 2594: 2537: 2496: 2486: 2444: 2395: 2351: 2258: 2248: 2182: 2157: 2116: 2075: 2065: 1970: 1929: 1888: 1796: 1712: 1702: 1661: 1651: 1575: 1565: 183: 3015: 2937:Satoh MS, Hanawalt PC (September 1996). 444: 385: 240: 202: 20: 711: 3535: 1819: 344: 3068: 2048:Mittal RD, Mandal RK (January 2012). 1771:Zhang Y, Rohde LH, Wu H (June 2009). 634:In humans, mutational defects in the 237:Transcription coupled repair (TC-NER) 193: 79:(UV). UV DNA damage results in bulky 2826:"Changes in DNA repair during aging" 461:risk by affecting repair efficacy. 320:activity; it cuts DNA damage on the 1861:Human & Experimental Toxicology 673:Cockayne syndrome (CS) arises from 616:(XPB) gene can lead, in humans, to 437:interaction with the UvrA subunit. 13: 3395:Proliferating Cell Nuclear Antigen 3326:Microhomology-mediated end joining 2910: 1634:Le May N, Egly JM, Coin F (2010). 771:CDK Activator Kinase (CAK) subunit 355:Proliferating Cell Nuclear Antigen 14: 3554: 3046: 126:, which express enzymes like the 3517: 3516: 3410:Meiotic recombination checkpoint 3052: 2773:Edifizi D, Schumacher B (2015). 2274: 2054:Indian Journal of Human Genetics 1608:Introduction to genetic analysis 1591: 1548:Fuss JO, Cooper PK (June 2006). 895:Damage recognition; recruits XPC 786:Cyclin Dependent Kinase (CDK) 7) 336:Replication protein A (RPA) and 292: 113: 2922:. Washington, D.C.: ASM Press. 2146:International Journal of Cancer 463:Single-nucleotide polymorphisms 3094: 1: 3000:10.1016/S1097-2765(02)00732-3 2207:10.1016/S0027-5107(02)00219-1 1834:10.1016/S1357-4310(99)01601-9 1535: 3292:Transcription-coupled repair 3030:10.1016/j.mrfmmm.2005.03.016 2643:10.1371/journal.pgen.1004686 2587:10.1016/j.dnarep.2011.04.026 2437:10.1016/j.dnarep.2011.04.028 1567:10.1371/journal.pbio.0040203 376:In prokaryotes: Uvr proteins 288:-like features, microcephaly 7: 2675:Iyama T, Wilson DM (2016). 2419:Fuss JO, Tainer JA (2011). 1516: 372:the nicks to complete NER. 199:Global genomic NER (GG-NER) 83:— these adducts are mostly 10: 3561: 3314:Non-homologous end joining 3138:Nucleotide excision repair 3131:Poly ADP ribose polymerase 3059:Nucleotide excision repair 2920:DNA repair and mutagenesis 1789:10.2174/138920209788488544 668:DNA damage theory of aging 607:DNA damage theory of aging 500:Impact on cancer prognosis 379: 266:TC-NER associated diseases 224:GG-NER associated diseases 62:specific non-bulky lesions 30:Nucleotide excision repair 3512: 3377: 3356: 3284: 3229: 3102: 2693:10.1016/j.jmb.2015.11.020 2488:10.1016/j.ccr.2006.05.027 2016:10.1080/15287390902841029 1372:Transcription factor II H 703:Decline in NER with aging 620:(XP) or XP combined with 440: 298:Transcription factor II H 3309:Homology directed repair 3231:Homologous recombination 1881:10.1177/0960327112444476 1822:Molecular Medicine Today 1691:Journal of Nucleic Acids 1640:Journal of Nucleic Acids 512: 432:protein. TRCF is an SF2 367:Ligase-III-XRCC1 complex 2067:10.4103/0971-6866.96648 1972:10.1093/carcin/23.4.599 3331:Postreplication repair 3126:Uracil-DNA glycosylase 2955:10.1093/nar/24.18.3576 2943:Nucleic Acids Research 2250:10.1186/1471-2407-8-50 1357:Subunit of RFA complex 1324:Subunit of RFA complex 1192:Stabilizes CAK complex 595:sensorineural deafness 454: 391: 349:Replication factor C ( 246: 208: 130:. In humans and other 93:complementary sequence 26: 2892:10.1096/fj.14.10.1325 2118:10.1093/carcin/bgi055 640:xeroderma pigmentosum 618:xeroderma pigmentosum 583:xeroderma pigmentosum 570:DNA repair-deficient 448: 425:is a simple example. 389: 380:Further information: 244: 206: 156:хeroderma pigmentosum 104:Xeroderma pigmentosum 66:specific glycosylases 24: 3437:core protein complex 3112:Base excision repair 3061:at Wikimedia Commons 2397:10.4161/cc.5.24.3565 1523:Base excision repair 719:Human Gene (Protein) 712:NER associated genes 517:In humans and mice, 314:transcription bubble 54:base excision repair 42:intercalating agents 16:DNA repair mechanism 3209:DNA mismatch repair 2792:10.3390/biom5031855 2344:10.1038/nature19329 2336:2016Natur.537..427V 2008:2009JTEHA..72..698W 1873:2012HETox..31..981K 1704:10.4061/2010/179594 1653:10.4061/2010/616342 587:trichothiodystrophy 418:phosphodiester bond 402:UvrABC endonuclease 382:UvrABC endonuclease 363:Flap endonuclease 1 345:Repair and ligation 276:Trichothiodystrophy 108:Cockayne's syndrome 58:DNA mismatch repair 2842:10.1093/nar/gkm756 2575:DNA Repair (Amst.) 2539:10.1002/humu.20392 2425:DNA Repair (Amst.) 2002:(11–12): 698–705. 1505:Damage recognition 1472:Damage recognition 455: 392: 247: 209: 194:Damage recognition 27: 3530: 3529: 3405:Adaptive response 3057:Media related to 2949:(18): 3576–3582. 2929:978-1-55581-319-2 2830:Nucleic Acids Res 2330:(7620): 427–431. 2195:Mutation Research 2159:10.1002/ijc.23361 1750:10.1021/cr040471u 1617:978-0-7167-6887-6 1514: 1513: 680:in either of two 644:Cockayne syndrome 622:Cockayne syndrome 612:Mutations in the 591:Cockayne syndrome 577:Mutations in the 519:germline mutation 416:. UvrB cleaves a 410:pyrimidine dimers 282:Cockayne syndrome 132:placental animals 77:ultraviolet light 3550: 3520: 3519: 3089: 3082: 3075: 3066: 3065: 3056: 3041: 3024:(1–2): 155–161. 3012: 3002: 2993:(6): 1391–1401. 2976: 2966: 2933: 2905: 2904: 2894: 2870: 2864: 2863: 2853: 2821: 2815: 2814: 2804: 2794: 2770: 2764: 2763: 2753: 2742:10.4161/cc.29018 2721: 2715: 2714: 2704: 2672: 2666: 2665: 2655: 2645: 2636:(10): e1004686. 2620: 2609: 2608: 2598: 2566: 2560: 2559: 2541: 2532:(11): 1092–103. 2517: 2511: 2510: 2500: 2490: 2465: 2459: 2458: 2448: 2416: 2410: 2409: 2399: 2375: 2366: 2365: 2355: 2314: 2308: 2307: 2298:(4): 1354–1357. 2286: 2280: 2279: 2278: 2272: 2262: 2252: 2228: 2219: 2218: 2201:(1–2): 165–174. 2189: 2180: 2179: 2161: 2152:(9): 2101–2105. 2137: 2131: 2130: 2120: 2111:(6): 1085–1090. 2096: 2090: 2089: 2079: 2069: 2045: 2036: 2035: 1991: 1985: 1984: 1974: 1950: 1944: 1943: 1933: 1909: 1903: 1902: 1892: 1867:(10): 981–1005. 1852: 1846: 1845: 1817: 1811: 1810: 1800: 1777:Current Genomics 1768: 1762: 1761: 1738:Chemical Reviews 1733: 1727: 1726: 1716: 1706: 1682: 1676: 1675: 1665: 1655: 1631: 1622: 1621: 1603: 1597: 1596: 1595: 1589: 1579: 1569: 1545: 716: 715: 397:Escherichia coli 154:all derive from 3560: 3559: 3553: 3552: 3551: 3549: 3548: 3547: 3533: 3532: 3531: 3526: 3508: 3378:Other/ungrouped 3373: 3352: 3280: 3225: 3121:DNA glycosylase 3104:Excision repair 3098: 3093: 3049: 3044: 2930: 2913: 2911:Further reading 2908: 2885:(10): 1325–34. 2871: 2867: 2836:(22): 7466–74. 2822: 2818: 2771: 2767: 2736:(13): 2029–37. 2722: 2718: 2673: 2669: 2621: 2612: 2567: 2563: 2518: 2514: 2466: 2462: 2417: 2413: 2376: 2369: 2315: 2311: 2292:Cancer Research 2287: 2283: 2273: 2229: 2222: 2190: 2183: 2138: 2134: 2097: 2093: 2046: 2039: 1992: 1988: 1951: 1947: 1910: 1906: 1853: 1849: 1828:(12): 538–543. 1818: 1814: 1769: 1765: 1734: 1730: 1683: 1679: 1632: 1625: 1618: 1604: 1600: 1590: 1546: 1542: 1538: 1529:Mismatch repair 1519: 737:Function in NER 714: 705: 515: 502: 485: 443: 384: 378: 347: 324:side while the 295: 268: 239: 226: 201: 196: 116: 17: 12: 11: 5: 3558: 3557: 3546: 3545: 3528: 3527: 3525: 3524: 3513: 3510: 3509: 3507: 3506: 3501: 3496: 3491: 3486: 3481: 3480: 3479: 3474: 3469: 3464: 3459: 3454: 3449: 3444: 3429: 3428: 3423: 3413: 3412: 3407: 3402: 3397: 3392: 3387: 3381: 3379: 3375: 3374: 3372: 3371: 3366: 3360: 3358: 3354: 3353: 3351: 3350: 3349: 3348: 3343: 3333: 3328: 3323: 3322: 3321: 3311: 3306: 3305: 3304: 3299: 3288: 3286: 3285:Other pathways 3282: 3281: 3279: 3278: 3273: 3268: 3263: 3258: 3257: 3256: 3246: 3241: 3235: 3233: 3227: 3226: 3224: 3223: 3222: 3221: 3216: 3206: 3205: 3204: 3199: 3194: 3189: 3184: 3179: 3174: 3169: 3164: 3159: 3154: 3149: 3135: 3134: 3133: 3128: 3123: 3108: 3106: 3100: 3099: 3092: 3091: 3084: 3077: 3069: 3063: 3062: 3048: 3047:External links 3045: 3043: 3042: 3013: 2978: 2934: 2928: 2914: 2912: 2909: 2907: 2906: 2865: 2816: 2785:(3): 1855–69. 2765: 2716: 2667: 2610: 2561: 2512: 2460: 2431:(7): 697–713. 2411: 2390:(24): 2886–8. 2367: 2309: 2281: 2220: 2181: 2132: 2105:Carcinogenesis 2091: 2037: 1986: 1965:(4): 599–603. 1959:Carcinogenesis 1945: 1904: 1847: 1812: 1783:(4): 250–258. 1763: 1744:(2): 233–252. 1728: 1677: 1623: 1616: 1598: 1539: 1537: 1534: 1533: 1532: 1526: 1518: 1515: 1512: 1511: 1506: 1503: 1500: 1495: 1490: 1479: 1478: 1473: 1470: 1467: 1462: 1457: 1446: 1445: 1440: 1437: 1434: 1429: 1424: 1413: 1412: 1401: 1398: 1395: 1384: 1375: 1364: 1363: 1358: 1355: 1352: 1347: 1342: 1331: 1330: 1325: 1322: 1319: 1314: 1309: 1298: 1297: 1292: 1289: 1286: 1281: 1276: 1265: 1264: 1259: 1256: 1253: 1248: 1243: 1232: 1231: 1226: 1223: 1220: 1215: 1210: 1199: 1198: 1193: 1190: 1187: 1182: 1177: 1166: 1165: 1160: 1159:Final ligation 1157: 1154: 1149: 1144: 1133: 1132: 1127: 1124: 1121: 1116: 1111: 1100: 1099: 1094: 1091: 1088: 1083: 1078: 1067: 1066: 1061: 1058: 1055: 1050: 1045: 1034: 1033: 1028: 1025: 1022: 1017: 1012: 1001: 1000: 995: 992: 989: 984: 979: 968: 967: 962: 959: 956: 951: 946: 935: 934: 929: 926: 923: 918: 913: 902: 901: 896: 893: 890: 887: 882: 871: 870: 865: 862: 859: 856: 851: 840: 839: 834: 831: 828: 825: 820: 811: 810: 805: 802: 799: 794: 789: 778: 777: 772: 769: 766: 761: 756: 745: 744: 738: 735: 732: 726: 720: 713: 710: 704: 701: 627:Deficiency of 514: 511: 501: 498: 484: 481: 442: 439: 377: 374: 346: 343: 294: 291: 290: 289: 279: 267: 264: 256:RNA polymerase 238: 235: 234: 233: 225: 222: 200: 197: 195: 192: 115: 112: 89:DNA polymerase 85:thymine dimers 15: 9: 6: 4: 3: 2: 3556: 3555: 3544: 3541: 3540: 3538: 3523: 3515: 3514: 3511: 3505: 3502: 3500: 3497: 3495: 3492: 3490: 3487: 3485: 3482: 3478: 3475: 3473: 3470: 3468: 3465: 3463: 3460: 3458: 3455: 3453: 3450: 3448: 3445: 3443: 3440: 3439: 3438: 3434: 3433:FANC proteins 3431: 3430: 3427: 3424: 3422: 3418: 3415: 3414: 3411: 3408: 3406: 3403: 3401: 3398: 3396: 3393: 3391: 3388: 3386: 3383: 3382: 3380: 3376: 3370: 3367: 3365: 3362: 3361: 3359: 3355: 3347: 3344: 3342: 3339: 3338: 3337: 3334: 3332: 3329: 3327: 3324: 3320: 3317: 3316: 3315: 3312: 3310: 3307: 3303: 3300: 3298: 3295: 3294: 3293: 3290: 3289: 3287: 3283: 3277: 3274: 3272: 3269: 3267: 3264: 3262: 3259: 3255: 3254:RecQ helicase 3252: 3251: 3250: 3247: 3245: 3242: 3240: 3237: 3236: 3234: 3232: 3228: 3220: 3217: 3215: 3212: 3211: 3210: 3207: 3203: 3200: 3198: 3195: 3193: 3190: 3188: 3185: 3183: 3180: 3178: 3175: 3173: 3170: 3168: 3165: 3163: 3160: 3158: 3155: 3153: 3150: 3148: 3145: 3144: 3143: 3139: 3136: 3132: 3129: 3127: 3124: 3122: 3119: 3118: 3117: 3113: 3110: 3109: 3107: 3105: 3101: 3097: 3090: 3085: 3083: 3078: 3076: 3071: 3070: 3067: 3060: 3055: 3051: 3050: 3039: 3035: 3031: 3027: 3023: 3019: 3014: 3010: 3006: 3001: 2996: 2992: 2988: 2984: 2979: 2974: 2970: 2965: 2960: 2956: 2952: 2948: 2944: 2940: 2935: 2931: 2925: 2921: 2916: 2915: 2902: 2898: 2893: 2888: 2884: 2880: 2876: 2869: 2861: 2857: 2852: 2847: 2843: 2839: 2835: 2831: 2827: 2820: 2812: 2808: 2803: 2798: 2793: 2788: 2784: 2780: 2776: 2769: 2761: 2757: 2752: 2747: 2743: 2739: 2735: 2731: 2727: 2720: 2712: 2708: 2703: 2698: 2694: 2690: 2686: 2682: 2678: 2671: 2663: 2659: 2654: 2649: 2644: 2639: 2635: 2631: 2627: 2619: 2617: 2615: 2606: 2602: 2597: 2592: 2588: 2584: 2581:(7): 781–91. 2580: 2576: 2572: 2565: 2557: 2553: 2549: 2545: 2540: 2535: 2531: 2527: 2523: 2516: 2508: 2504: 2499: 2494: 2489: 2484: 2481:(2): 121–32. 2480: 2476: 2472: 2464: 2456: 2452: 2447: 2442: 2438: 2434: 2430: 2426: 2422: 2415: 2407: 2403: 2398: 2393: 2389: 2385: 2381: 2374: 2372: 2363: 2359: 2354: 2349: 2345: 2341: 2337: 2333: 2329: 2325: 2321: 2313: 2305: 2301: 2297: 2293: 2285: 2277: 2270: 2266: 2261: 2256: 2251: 2246: 2242: 2238: 2234: 2227: 2225: 2216: 2212: 2208: 2204: 2200: 2196: 2188: 2186: 2177: 2173: 2169: 2165: 2160: 2155: 2151: 2147: 2143: 2136: 2128: 2124: 2119: 2114: 2110: 2106: 2102: 2095: 2087: 2083: 2078: 2073: 2068: 2063: 2059: 2055: 2051: 2044: 2042: 2033: 2029: 2025: 2021: 2017: 2013: 2009: 2005: 2001: 1997: 1990: 1982: 1978: 1973: 1968: 1964: 1960: 1956: 1949: 1941: 1937: 1932: 1927: 1923: 1919: 1915: 1908: 1900: 1896: 1891: 1886: 1882: 1878: 1874: 1870: 1866: 1862: 1858: 1851: 1843: 1839: 1835: 1831: 1827: 1823: 1816: 1808: 1804: 1799: 1794: 1790: 1786: 1782: 1778: 1774: 1767: 1759: 1755: 1751: 1747: 1743: 1739: 1732: 1724: 1720: 1715: 1710: 1705: 1700: 1696: 1692: 1688: 1681: 1673: 1669: 1664: 1659: 1654: 1649: 1645: 1641: 1637: 1630: 1628: 1619: 1613: 1609: 1602: 1594: 1587: 1583: 1578: 1573: 1568: 1563: 1559: 1555: 1551: 1544: 1540: 1530: 1527: 1524: 1521: 1520: 1510: 1507: 1504: 1501: 1499: 1496: 1494: 1491: 1488: 1484: 1481: 1480: 1477: 1474: 1471: 1468: 1466: 1463: 1461: 1458: 1455: 1451: 1448: 1447: 1444: 1441: 1438: 1435: 1433: 1430: 1428: 1425: 1422: 1418: 1415: 1414: 1411: 1408: 1405: 1402: 1399: 1396: 1394: 1391: 1388: 1385: 1383: 1379: 1376: 1373: 1369: 1366: 1365: 1362: 1359: 1356: 1353: 1351: 1348: 1346: 1343: 1340: 1336: 1333: 1332: 1329: 1326: 1323: 1320: 1318: 1315: 1313: 1310: 1307: 1303: 1300: 1299: 1296: 1293: 1290: 1287: 1285: 1282: 1280: 1277: 1274: 1270: 1267: 1266: 1263: 1260: 1257: 1254: 1252: 1249: 1247: 1244: 1241: 1237: 1234: 1233: 1230: 1227: 1224: 1221: 1219: 1216: 1214: 1211: 1208: 1204: 1201: 1200: 1197: 1194: 1191: 1188: 1186: 1183: 1181: 1178: 1175: 1171: 1168: 1167: 1164: 1161: 1158: 1155: 1153: 1150: 1148: 1145: 1142: 1138: 1135: 1134: 1131: 1128: 1125: 1122: 1120: 1117: 1115: 1112: 1109: 1105: 1102: 1101: 1098: 1095: 1092: 1089: 1087: 1084: 1082: 1079: 1076: 1072: 1069: 1068: 1065: 1062: 1059: 1056: 1054: 1051: 1049: 1046: 1043: 1039: 1036: 1035: 1032: 1029: 1026: 1023: 1021: 1018: 1016: 1013: 1010: 1006: 1003: 1002: 999: 996: 993: 990: 988: 985: 983: 980: 977: 973: 970: 969: 966: 963: 960: 957: 955: 952: 950: 947: 944: 940: 937: 936: 933: 930: 927: 924: 922: 919: 917: 914: 911: 907: 904: 903: 900: 897: 894: 891: 888: 886: 883: 880: 876: 873: 872: 869: 866: 863: 860: 857: 855: 852: 849: 845: 842: 841: 838: 835: 832: 829: 826: 824: 821: 819: 816: 813: 812: 809: 806: 803: 800: 798: 795: 793: 790: 787: 783: 780: 779: 776: 773: 770: 767: 765: 762: 760: 757: 754: 750: 747: 746: 742: 739: 736: 733: 730: 727: 724: 721: 718: 717: 709: 700: 698: 694: 690: 686: 683: 679: 676: 671: 669: 665: 661: 657: 653: 649: 645: 641: 637: 632: 630: 625: 623: 619: 615: 610: 608: 604: 600: 596: 592: 588: 584: 580: 575: 573: 568: 566: 565: 560: 559: 554: 553: 548: 547: 542: 538: 534: 533: 528: 524: 520: 510: 508: 497: 494: 490: 480: 477: 473: 468: 464: 460: 452: 447: 438: 435: 431: 426: 424: 419: 415: 411: 407: 403: 399: 398: 388: 383: 373: 371: 368: 364: 360: 356: 352: 342: 339: 334: 331: 327: 323: 319: 315: 311: 307: 303: 299: 293:Dual incision 287: 283: 280: 277: 274: 273: 272: 263: 260: 257: 251: 243: 231: 230: 229: 221: 219: 215: 205: 191: 187: 185: 181: 177: 173: 169: 165: 161: 157: 153: 149: 145: 141: 137: 133: 129: 125: 121: 114:In eukaryotes 111: 109: 105: 100: 98: 94: 90: 86: 82: 78: 73: 71: 67: 63: 59: 55: 51: 47: 43: 39: 35: 31: 23: 19: 3436: 3417:DNA helicase 3400:8-Oxoguanine 3369:SOS response 3249:RecF pathway 3202:Excinuclease 3137: 3021: 3017: 2990: 2986: 2946: 2942: 2919: 2882: 2878: 2868: 2833: 2829: 2819: 2782: 2779:Biomolecules 2778: 2768: 2733: 2729: 2719: 2687:(1): 62–78. 2684: 2681:J. Mol. Biol 2680: 2670: 2633: 2629: 2578: 2574: 2564: 2529: 2525: 2515: 2478: 2474: 2463: 2428: 2424: 2414: 2387: 2383: 2327: 2323: 2312: 2295: 2291: 2284: 2240: 2236: 2198: 2194: 2149: 2145: 2135: 2108: 2104: 2094: 2060:(1): 47–55. 2057: 2053: 1999: 1995: 1989: 1962: 1958: 1948: 1921: 1917: 1907: 1864: 1860: 1850: 1825: 1821: 1815: 1780: 1776: 1766: 1741: 1737: 1731: 1694: 1690: 1680: 1643: 1639: 1607: 1601: 1557: 1554:PLOS Biology 1553: 1543: 1497: 1492: 1482: 1464: 1459: 1449: 1431: 1426: 1416: 1392: 1389: 1386: 1381: 1377: 1367: 1349: 1344: 1334: 1316: 1311: 1301: 1283: 1278: 1268: 1250: 1245: 1235: 1217: 1212: 1202: 1184: 1179: 1169: 1151: 1146: 1141:DNA Ligase I 1136: 1118: 1113: 1103: 1085: 1080: 1070: 1052: 1047: 1037: 1019: 1014: 1004: 986: 981: 971: 953: 948: 938: 920: 915: 905: 884: 874: 853: 843: 822: 814: 796: 791: 781: 763: 758: 748: 706: 696: 692: 688: 684: 672: 656:osteoporosis 647: 635: 633: 628: 626: 613: 611: 602: 578: 576: 571: 569: 562: 556: 550: 544: 536: 530: 522: 516: 503: 486: 472:phenotypical 456: 427: 422: 406:DNA helicase 395: 393: 359:DNA ligase I 353:) loads the 348: 335: 318:endonuclease 296: 269: 261: 252: 248: 227: 210: 188: 117: 101: 74: 29: 28: 18: 2475:Cancer Cell 1924:(1): 1–17. 1560:(6): e203. 818:(Centrin-2) 804:CAK subunit 507:lymphocytes 476:lung cancer 184:found below 150:, XPF, and 124:prokaryotes 81:DNA adducts 56:(BER), and 36:mechanism. 3543:DNA repair 3357:Regulation 3336:Photolyase 3096:DNA repair 3018:Mutat. Res 2730:Cell Cycle 2630:PLOS Genet 2526:Hum. Mutat 2498:10029/5565 2384:Cell Cycle 2237:BMC Cancer 1536:References 734:Subpathway 660:DNA damage 561:(CSB) and 467:DNA repair 451:DNA damage 430:TRCF (Mfd) 128:photolyase 120:eukaryotes 97:DNA ligase 70:base pairs 48:and other 34:DNA repair 3177:XPG/ERCC5 3162:XPD/ERCC2 2987:Mol. Cell 741:GeneCards 687:(CSA) or 678:mutations 46:radiation 3537:Category 3522:Category 3172:XPF/DDB1 3167:XPE/DDB1 3038:15913669 3009:12504014 2901:10877825 2860:17913742 2811:26287260 2760:24781187 2711:26616585 2662:25299392 2605:21612988 2556:22852219 2548:16947863 2507:16904611 2455:21571596 2406:17172862 2362:27556946 2304:11245433 2269:18267032 2215:12427537 2168:18196582 2127:15731165 2086:22754221 2032:22991719 2024:19492231 1981:11960912 1940:22493747 1899:23023028 1842:10562720 1807:19949546 1758:16464004 1723:20981145 1697:: 1–32. 1672:20725631 1646:: 1–10. 1586:16752948 1517:See also 885:Ddb2/Xpe 753:Cyclin H 731:Ortholog 725:Ortholog 675:germline 652:cachexia 624:(XPCS). 599:cachexia 286:progeria 50:mutagens 3364:SOS box 3116:AP site 2973:8836185 2879:FASEB J 2851:2190694 2802:4598778 2751:4111694 2702:4738086 2653:4191938 2596:3139823 2446:3234290 2353:5161687 2332:Bibcode 2260:2262891 2176:9456435 2077:3385179 2004:Bibcode 1931:3316453 1890:4586256 1869:Bibcode 1798:2709936 1714:2957137 1663:2915888 1577:1475692 889:Unknown 858:Unknown 827:Unknown 691:(CSB). 567:(CSA). 555:(XPG), 549:(XPF), 535:(XPD), 400:by the 365:or the 146:, XPD, 3489:FANCD2 3484:FANCD1 3244:RecBCD 3197:RAD23B 3192:RAD23A 3036:  3007:  2971:  2964:146147 2961:  2926:  2899:  2858:  2848:  2809:  2799:  2758:  2748:  2709:  2699:  2660:  2650:  2603:  2593:  2554:  2546:  2505:  2453:  2443:  2404:  2360:  2350:  2324:Nature 2302:  2267:  2257:  2243:: 50. 2213:  2174:  2166:  2125:  2084:  2074:  2030:  2022:  1979:  1938:  1928:  1897:  1887:  1840:  1805:  1795:  1756:  1721:  1711:  1670:  1660:  1614:  1584:  1574:  1436:TC-NER 1410:GTF2H3 1407:GTF2H2 1404:GTF2H1 1378:Gtf2h1 1295:RAD23B 1279:Rad23b 1273:RAD23B 1269:RAD23B 1262:RAD23A 1246:Rad23a 1240:RAD23A 1236:RAD23A 1123:TC-NER 1090:TC-NER 743:Entry 666:.(see 585:(XP), 459:cancer 441:Cancer 434:ATPase 423:E.coli 180:RAD23B 176:RAD23A 3504:FANCN 3499:FANCJ 3494:FANCI 3477:FANCM 3472:FANCL 3467:FANCG 3462:FANCF 3457:FANCE 3452:FANCC 3447:FANCB 3442:FANCA 3302:ERCC8 3297:ERCC6 3261:RAD51 3182:ERCC1 2552:S2CID 2172:S2CID 2028:S2CID 1531:(MMR) 1525:(BER) 1465:RAD14 1368:TFIIH 1284:RAD23 1251:RAD23 1229:MMS19 1218:MET18 1213:Mms19 1207:MMS19 1203:MMS19 1196:MNAT1 1180:Mnat1 1174:MNAT1 1170:MNAT1 1130:ERCC8 1119:RAD28 1114:Ercc8 1104:ERCC8 1097:ERCC6 1086:RAD26 1081:Ercc6 1071:ERCC6 1064:ERCC5 1048:Ercc5 1038:ERCC5 1031:ERCC4 1015:Ercc4 1005:ERCC4 998:ERCC3 987:RAD25 982:Ercc3 972:ERCC3 965:ERCC2 949:Ercc2 939:ERCC2 932:ERCC1 921:RAD10 916:Ercc1 910:ERCC1 906:ERCC1 837:CETN2 823:Cetn2 815:CETN2 797:KIN28 729:Yeast 723:Mouse 697:ERCC6 693:ERCC8 689:ERCC6 685:ERCC8 682:genes 664:aging 648:ERCC5 636:ERCC5 629:ERCC4 614:ERCC3 603:ERCC2 579:ERCC2 572:ERCC1 564:ERCC8 558:ERCC6 552:ERCC5 546:ERCC4 537:ERCC3 532:ERCC2 527:ERCC1 523:ERCC1 513:Aging 414:dimer 330:ERCC1 168:ERCC1 122:than 32:is a 3390:PcrA 3346:CRY2 3341:CRY1 3276:LexA 3271:Slx4 3266:Sgs1 3239:RecA 3219:MSH2 3214:MLH1 3142:ERCC 3034:PMID 3005:PMID 2969:PMID 2924:ISBN 2897:PMID 2856:PMID 2807:PMID 2756:PMID 2707:PMID 2658:PMID 2601:PMID 2544:PMID 2503:PMID 2451:PMID 2402:PMID 2358:PMID 2300:PMID 2265:PMID 2211:PMID 2164:PMID 2123:PMID 2082:PMID 2020:PMID 1977:PMID 1936:PMID 1895:PMID 1838:PMID 1803:PMID 1754:PMID 1719:PMID 1695:2010 1668:PMID 1644:2010 1612:ISBN 1582:PMID 1498:RAD4 1469:Both 1443:XAB2 1432:SYF1 1427:Xab2 1421:XAB2 1417:XAB2 1397:Both 1393:Tfb4 1390:Ssl1 1387:Tfb1 1361:RPA2 1354:Both 1350:RFA2 1345:Rpa2 1339:RPA2 1335:RPA2 1328:RPA1 1321:Both 1317:RFA1 1312:Rpa1 1306:RPA1 1302:RPA1 1222:Both 1189:Both 1185:TFB3 1163:LIG1 1156:Both 1152:CDC9 1147:Lig1 1137:LIG1 1057:Both 1053:RAD2 1024:Both 1020:RAD1 991:Both 958:Both 954:RAD3 925:Both 899:DDB2 879:DDB2 875:DDB2 868:DDB1 854:Ddb1 848:DDB1 844:DDB1 808:CDK7 801:Both 792:Cdk7 782:CDK7 775:CCNH 768:Both 764:CCL1 759:Ccnh 749:CCNH 662:and 654:and 491:and 370:seal 361:and 308:and 162:and 158:and 106:and 3426:WRN 3421:BLM 3385:Ogt 3187:RPA 3157:XPC 3152:XPB 3147:XPA 3026:doi 3022:577 2995:doi 2959:PMC 2951:doi 2887:doi 2846:PMC 2838:doi 2797:PMC 2787:doi 2746:PMC 2738:doi 2697:PMC 2689:doi 2685:428 2648:PMC 2638:doi 2591:PMC 2583:doi 2534:doi 2493:hdl 2483:doi 2441:PMC 2433:doi 2392:doi 2348:PMC 2340:doi 2328:537 2255:PMC 2245:doi 2203:doi 2199:509 2154:doi 2150:122 2113:doi 2072:PMC 2062:doi 2012:doi 1967:doi 1926:PMC 1885:PMC 1877:doi 1830:doi 1793:PMC 1785:doi 1746:doi 1742:106 1709:PMC 1699:doi 1658:PMC 1648:doi 1572:PMC 1562:doi 1509:XPC 1502:GGR 1493:Xpc 1487:XPC 1483:XPC 1476:XPA 1460:Xpa 1454:XPA 1450:XPA 1288:GGR 1255:GGR 1108:CSA 1075:CSB 1042:XPG 1009:XPF 976:XPB 943:XPD 892:GGR 861:GGR 830:GGR 670:). 609:). 543:), 541:XPB 529:), 493:XPC 489:XPD 351:RFC 338:XPA 326:XPF 310:XPB 306:XPD 302:XPG 218:XPE 214:XPC 172:RPA 164:CSB 160:CSA 152:XPG 148:XPE 144:XPC 140:XPB 136:XPA 44:), 38:DNA 3539:: 3435:: 3419:: 3319:Ku 3032:. 3020:. 3003:. 2991:10 2989:. 2985:. 2967:. 2957:. 2947:24 2945:. 2941:. 2895:. 2883:14 2881:. 2877:. 2854:. 2844:. 2834:35 2832:. 2828:. 2805:. 2795:. 2781:. 2777:. 2754:. 2744:. 2734:13 2732:. 2728:. 2705:. 2695:. 2683:. 2679:. 2656:. 2646:. 2634:10 2632:. 2628:. 2613:^ 2599:. 2589:. 2579:10 2577:. 2573:. 2550:. 2542:. 2530:27 2528:. 2524:. 2501:. 2491:. 2479:10 2477:. 2473:. 2449:. 2439:. 2429:10 2427:. 2423:. 2400:. 2386:. 2382:. 2370:^ 2356:. 2346:. 2338:. 2326:. 2322:. 2296:61 2294:. 2263:. 2253:. 2239:. 2235:. 2223:^ 2209:. 2197:. 2184:^ 2170:. 2162:. 2148:. 2144:. 2121:. 2109:26 2107:. 2103:. 2080:. 2070:. 2058:18 2056:. 2052:. 2040:^ 2026:. 2018:. 2010:. 2000:72 1998:. 1975:. 1963:23 1961:. 1957:. 1934:. 1920:. 1916:. 1893:. 1883:. 1875:. 1865:31 1863:. 1859:. 1836:. 1824:. 1801:. 1791:. 1781:10 1779:. 1775:. 1752:. 1740:. 1717:. 1707:. 1693:. 1689:. 1666:. 1656:. 1642:. 1638:. 1626:^ 1580:. 1570:. 1556:. 1552:. 322:3' 186:. 178:, 174:, 170:, 142:, 138:, 72:. 3140:/ 3114:/ 3088:e 3081:t 3074:v 3040:. 3028:: 3011:. 2997:: 2975:. 2953:: 2932:. 2903:. 2889:: 2862:. 2840:: 2813:. 2789:: 2783:5 2762:. 2740:: 2713:. 2691:: 2664:. 2640:: 2607:. 2585:: 2558:. 2536:: 2509:. 2495:: 2485:: 2457:. 2435:: 2408:. 2394:: 2388:5 2364:. 2342:: 2334:: 2306:. 2271:. 2247:: 2241:8 2217:. 2205:: 2178:. 2156:: 2129:. 2115:: 2088:. 2064:: 2034:. 2014:: 2006:: 1983:. 1969:: 1942:. 1922:3 1901:. 1879:: 1871:: 1844:. 1832:: 1826:5 1809:. 1787:: 1760:. 1748:: 1725:. 1701:: 1674:. 1650:: 1620:. 1588:. 1564:: 1558:4 1489:) 1485:( 1456:) 1452:( 1423:) 1419:( 1382:3 1380:- 1374:) 1370:( 1341:) 1337:( 1308:) 1304:( 1275:) 1271:( 1242:) 1238:( 1209:) 1205:( 1176:) 1172:( 1143:) 1139:( 1110:) 1106:( 1077:) 1073:( 1044:) 1040:( 1011:) 1007:( 978:) 974:( 945:) 941:( 912:) 908:( 881:) 877:( 850:) 846:( 788:) 784:( 755:) 751:( 539:( 525:( 328:–

Index


DNA repair
DNA
intercalating agents
radiation
mutagens
base excision repair
DNA mismatch repair
specific non-bulky lesions
specific glycosylases
base pairs
ultraviolet light
DNA adducts
thymine dimers
DNA polymerase
complementary sequence
DNA ligase
Xeroderma pigmentosum
Cockayne's syndrome
eukaryotes
prokaryotes
photolyase
placental animals
XPA
XPB
XPC
XPE
XPG
хeroderma pigmentosum
CSA

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