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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.
215: 3529: 231:) 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. 3065: 520:. 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. 260:
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.
110:. 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. 264:
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
710:(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. 489:
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".
397: 476:(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 669:
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
2244:"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" 616:(XPD) mutant human and mouse show evidence of defective repair of oxidative DNA damages that may underlie the segmental progeroid (premature aging) symptoms (see 423:. 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 323:
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
2432:"XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase" 3462: 2950:"TFIIH-mediated nucleotide excision repair and initiation of mRNA transcription in an optimized cell-free DNA repair and RNA transcription assay" 2531:
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).
145:, there are 9 major proteins involved in NER. Deficiencies in certain proteins leads to disease; protein names are associated with the disease. 3436: 2061:"Genetic variation in nucleotide excision repair pathway genes influence prostate and bladder cancer susceptibility in North Indian population" 2938: 1626: 368:(PCNA) onto the DNA strand. This allows DNA polymerases implicated in repair (δ, ε and/or κ) to copy the undamaged strand via translocation. 3097: 2482:"An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria" 3069: 3152: 468:
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".
670: 464:. Unrepaired damage or malfunctioning proteins associated with excision repair could lead to unregulated cell growth and cancer. 2151:
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.
2737:"Cockayne syndrome protein A is a transcription factor of RNA polymerase I and stimulates ribosomal biogenesis and growth" 243:
Xeroderma pigmentosum (XP): severe photosensitivity, high cancer rates in areas of the body exposed to the sun (e.g. skin)
2533:"Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome" 3395: 3302: 52: 2112:"Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: a case-control study" 3324: 3141: 678: 617: 605: 440: 86:
Nucleotide excision repair (NER) is a particularly important excision mechanism that removes DNA damage induced by
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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
308: 193:, and others also participate in nucleotide excision repair. A more complete list of proteins involved in NER is 3319: 3241: 3090: 739: 63:. Three excision repair pathways exist to repair single stranded DNA damage: Nucleotide excision repair (NER), 36:
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, Schäfer P, Scharffetter-Kochanek K, Iben S (2014).
2637:"Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency" 1966:"The XPD variant alleles are associated with increased aromatic DNA adduct level and lung cancer risk" 1647:"True lies: the double life of the nucleotide excision repair factors in transcription and DNA repair" 3122: 2342: 2014: 1879: 1533: 361: 324: 76: 72: 64: 3553: 3532: 3219: 3083: 1539: 597: 428: 412: 392: 373: 286: 68: 2562: 2182: 2038: 1784:"Involvement of nucleotide excision and mismatch repair mechanisms in double strand break repair" 252: 3415: 3044: 3015: 2979: 2934: 2907: 2866: 2817: 2766: 2717: 2668: 2611: 2554: 2513: 2461: 2412: 2368: 2310: 2275: 2221: 2174: 2133: 2092: 2030: 1987: 1946: 1905: 1848: 1813: 1764: 1729: 1678: 1622: 1592: 654: 632: 601: 529: 424: 292: 118: 87: 1104:
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.
214: 3547: 3443: 3264: 1868:"Impact of DNA polymorphisms in key DNA base excision repair proteins on cancer risk" 162: 95: 2566: 2042: 3410: 3379: 3329: 3312: 3259: 3212: 2886:"Mechanisms and implications of the age-associated decrease in DNA repair capacity" 2186: 1118: 666: 574: 482: 416: 369: 328: 289:(TTD): some individuals are photosensitive, ichthyosis, mental/physical retardation 1964:
Hou SM, Fält S, Angelini S, Yang K, Nyberg F, Lambert B, Hemminki K (April 2002).
106:. Final ligation to complete NER and form a double stranded DNA is carried out by 3040: 2653: 2597: 2447: 1577: 2992:
Frit P, Kwon K, Coin F, Auriol J, Dubaele S, Salles B, Egly JM (December 2002).
733: 642:(XPF) in humans results in a variety of conditions including accelerated aging. 486: 227:-Rad23B complex is responsible for distortion recognition, while DDB1 and DDB2 ( 142: 2391:"Nucleotide excision repair disorders and the balance between cancer and aging" 1799: 223:
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
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ATPase and helicase activity; transcription factor II H (TFIIH) subunit
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ATPase and helicase activity; transcription factor II H (TFIIH) subunit
828: 706:(CSA) mutations generally give rise to a more moderate form of CS than 657:(CS) or the infantile lethal cerebro-oculo-facio-skeletal syndrome. An 60: 2884:
Goukassian D, Gad F, Yaar M, Eller MS, Nehal US, Gilchrest BA (2000).
2508: 2169: 2153:"Polymorphisms in XPC and ERCC2 genes, smoking and breast cancer risk" 2152: 1760: 273:
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
612:(loss of subcutaneous fat tissue). XPCS and TTD fibroblasts from 3400: 3356: 3351: 3286: 3281: 3276: 3249: 3229: 3224: 3177: 1431: 1349: 1316: 1151: 889: 858: 692: 3079: 311:(TFIIH) is the key enzyme involved in dual excision. TFIIH and 3162: 3157: 1464: 986: 551: 348: 320: 150: 146: 75:
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.
1561:"DNA repair: dynamic defenders against cancer and aging" 649:(XPG) gene can cause either the cancer-prone condition 439:
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.
3388: 3367: 3295: 3240: 3113: 1696:Morita R, Nakane S, Shimada A, et al. (2010). 2389:Andressoo JO, Hoeijmakers JH, Mitchell JR (2006). 2994:"Transcriptional activators stimulate DNA repair" 1411:Involved in incision, forms complex around lesion 592:(XPD) gene can lead to various syndromes, either 327:. In addition to stabilizing TFIIH, XPG also has 2835:Gorbunova V, Seluanov A, Mao Z, Hine C (2007). 2629: 2627: 2625: 2580:Gregg SQ, Robinson AR, Niedernhofer LJ (2011). 2384: 2382: 460:DNA excision pathways work in tandem to repair 1866:Karahalil B, Bohr V, Wilson D (October 2012). 1640: 1638: 1621:. New York: W.H. Freeman and Co. p. 534. 201:steps of dual incision, repair, and ligation. 129:Nucleotide excision repair is more complex in 3091: 2988:Article on the relation between TFIIH and NER 2237: 2235: 121:are two examples of NER associated diseases. 8: 2198: 2196: 295:(CS): photosensitivity, mental retardation, 102:uses it as a template to synthesize a short 875:Damage recognition; forms complex with DDB2 71:(MMR). While the BER pathway can recognize 3098: 3084: 3076: 1302:Damage recognition, forms complex with XPC 1269:Damage recognition; forms complex with XPC 844:Damage recognition; forms complex with XPC 726: 494:NER dysfunction result of DNA polymorphism 3009: 2973: 2901: 2860: 2811: 2801: 2760: 2711: 2662: 2652: 2605: 2548: 2507: 2497: 2455: 2406: 2362: 2269: 2259: 2168: 2127: 2086: 2076: 1981: 1940: 1899: 1807: 1723: 1713: 1672: 1662: 1586: 1576: 194: 2948:Satoh MS, Hanawalt PC (September 1996). 455: 251: 31: 1551: 2059:Mittal RD, Mandal RK (January 2012). 1782:Zhang Y, Rohde LH, Wu H (June 2009). 645:In humans, mutational defects in the 248:Transcription coupled repair (TC-NER) 90:(UV). UV DNA damage results in bulky 7: 2837:"Changes in DNA repair during aging" 472:risk by affecting repair efficacy. 331:activity; it cuts DNA damage on the 1872:Human & Experimental Toxicology 684:Cockayne syndrome (CS) arises from 627:(XPB) gene can lead, in humans, to 448:interaction with the UvrA subunit. 3406:Proliferating Cell Nuclear Antigen 3337:Microhomology-mediated end joining 1645:Le May N, Egly JM, Coin F (2010). 782:CDK Activator Kinase (CAK) subunit 366:Proliferating Cell Nuclear Antigen 25: 137:, which express enzymes like the 3528: 3527: 3421:Meiotic recombination checkpoint 3063: 2784:Edifizi D, Schumacher B (2015). 2285: 2065:Indian Journal of Human Genetics 1619:Introduction to genetic analysis 1602: 1559:Fuss JO, Cooper PK (June 2006). 906:Damage recognition; recruits XPC 797:Cyclin Dependent Kinase (CDK) 7) 347:Replication protein A (RPA) and 2933:. Washington, D.C.: ASM Press. 2157:International Journal of Cancer 474:Single-nucleotide polymorphisms 1: 3011:10.1016/S1097-2765(02)00732-3 2218:10.1016/S0027-5107(02)00219-1 1845:10.1016/S1357-4310(99)01601-9 3303:Transcription-coupled repair 3041:10.1016/j.mrfmmm.2005.03.016 2654:10.1371/journal.pgen.1004686 2598:10.1016/j.dnarep.2011.04.026 2448:10.1016/j.dnarep.2011.04.028 1578:10.1371/journal.pbio.0040203 387:In prokaryotes: Uvr proteins 299:-like features, microcephaly 18:Transcription-coupled repair 2686:Iyama T, Wilson DM (2016). 2430:Fuss JO, Tainer JA (2011). 383:the nicks to complete NER. 210:Global genomic NER (GG-NER) 94:— these adducts are mostly 3570: 3325:Non-homologous end joining 3149:Nucleotide excision repair 3142:Poly ADP ribose polymerase 3070:Nucleotide excision repair 2931:DNA repair and mutagenesis 1800:10.2174/138920209788488544 679:DNA damage theory of aging 618:DNA damage theory of aging 511:Impact on cancer prognosis 390: 277:TC-NER associated diseases 235:GG-NER associated diseases 73:specific non-bulky lesions 41:Nucleotide excision repair 3523: 2704:10.1016/j.jmb.2015.11.020 2499:10.1016/j.ccr.2006.05.027 2027:10.1080/15287390902841029 1383:Transcription factor II H 714:Decline in NER with aging 631:(XP) or XP combined with 309:Transcription factor II H 3320:Homology directed repair 3242:Homologous recombination 1892:10.1177/0960327112444476 1833:Molecular Medicine Today 1702:Journal of Nucleic Acids 1651:Journal of Nucleic Acids 443:protein. TRCF is an SF2 378:Ligase-III-XRCC1 complex 2078:10.4103/0971-6866.96648 1983:10.1093/carcin/23.4.599 3342:Postreplication repair 3137:Uracil-DNA glycosylase 2966:10.1093/nar/24.18.3576 2954:Nucleic Acids Research 2261:10.1186/1471-2407-8-50 1368:Subunit of RFA complex 1335:Subunit of RFA complex 1203:Stabilizes CAK complex 606:sensorineural deafness 465: 402: 360:Replication factor C ( 257: 219: 141:. In humans and other 104:complementary sequence 37: 2903:10.1096/fj.14.10.1325 2129:10.1093/carcin/bgi055 651:xeroderma pigmentosum 629:xeroderma pigmentosum 594:xeroderma pigmentosum 581:DNA repair-deficient 459: 436:is a simple example. 400: 391:Further information: 255: 217: 167:хeroderma pigmentosum 115:Xeroderma pigmentosum 77:specific glycosylases 35: 3448:core protein complex 3123:Base excision repair 3072:at Wikimedia Commons 2408:10.4161/cc.5.24.3565 1534:Base excision repair 730:Human Gene (Protein) 723:NER associated genes 528:In humans and mice, 325:transcription bubble 65:base excision repair 53:intercalating agents 27:DNA repair mechanism 3220:DNA mismatch repair 2803:10.3390/biom5031855 2355:10.1038/nature19329 2347:2016Natur.537..427V 2019:2009JTEHA..72..698W 1884:2012HETox..31..981K 1715:10.4061/2010/179594 1664:10.4061/2010/616342 598:trichothiodystrophy 429:phosphodiester bond 413:UvrABC endonuclease 393:UvrABC endonuclease 374:Flap endonuclease 1 356:Repair and ligation 287:Trichothiodystrophy 119:Cockayne's syndrome 69:DNA mismatch repair 2853:10.1093/nar/gkm756 2586:DNA Repair (Amst.) 2550:10.1002/humu.20392 2436:DNA Repair (Amst.) 2013:(11–12): 698–705. 1516:Damage recognition 1483:Damage recognition 466: 403: 258: 220: 205:Damage recognition 38: 3541: 3540: 3416:Adaptive response 3068:Media related to 2960:(18): 3576–3582. 2940:978-1-55581-319-2 2841:Nucleic Acids Res 2341:(7620): 427–431. 2206:Mutation Research 2170:10.1002/ijc.23361 1761:10.1021/cr040471u 1628:978-0-7167-6887-6 1525: 1524: 691:in either of two 655:Cockayne syndrome 633:Cockayne syndrome 623:Mutations in the 602:Cockayne syndrome 588:Mutations in the 530:germline mutation 427:. UvrB cleaves a 421:pyrimidine dimers 293:Cockayne syndrome 143:placental animals 88:ultraviolet light 16:(Redirected from 3561: 3531: 3530: 3100: 3093: 3086: 3077: 3067: 3052: 3035:(1–2): 155–161. 3023: 3013: 3004:(6): 1391–1401. 2987: 2977: 2944: 2916: 2915: 2905: 2881: 2875: 2874: 2864: 2832: 2826: 2825: 2815: 2805: 2781: 2775: 2774: 2764: 2753:10.4161/cc.29018 2732: 2726: 2725: 2715: 2683: 2677: 2676: 2666: 2656: 2647:(10): e1004686. 2631: 2620: 2619: 2609: 2577: 2571: 2570: 2552: 2543:(11): 1092–103. 2528: 2522: 2521: 2511: 2501: 2476: 2470: 2469: 2459: 2427: 2421: 2420: 2410: 2386: 2377: 2376: 2366: 2325: 2319: 2318: 2309:(4): 1354–1357. 2297: 2291: 2290: 2289: 2283: 2273: 2263: 2239: 2230: 2229: 2212:(1–2): 165–174. 2200: 2191: 2190: 2172: 2163:(9): 2101–2105. 2148: 2142: 2141: 2131: 2122:(6): 1085–1090. 2107: 2101: 2100: 2090: 2080: 2056: 2047: 2046: 2002: 1996: 1995: 1985: 1961: 1955: 1954: 1944: 1920: 1914: 1913: 1903: 1878:(10): 981–1005. 1863: 1857: 1856: 1828: 1822: 1821: 1811: 1788:Current Genomics 1779: 1773: 1772: 1749:Chemical Reviews 1744: 1738: 1737: 1727: 1717: 1693: 1687: 1686: 1676: 1666: 1642: 1633: 1632: 1614: 1608: 1607: 1606: 1600: 1590: 1580: 1556: 727: 408:Escherichia coli 165:all derive from 21: 3569: 3568: 3564: 3563: 3562: 3560: 3559: 3558: 3544: 3543: 3542: 3537: 3519: 3389:Other/ungrouped 3384: 3363: 3291: 3236: 3132:DNA glycosylase 3115:Excision repair 3109: 3104: 3060: 3055: 3026: 2991: 2947: 2941: 2928: 2924: 2922:Further reading 2919: 2896:(10): 1325–34. 2883: 2882: 2878: 2847:(22): 7466–74. 2834: 2833: 2829: 2783: 2782: 2778: 2747:(13): 2029–37. 2734: 2733: 2729: 2685: 2684: 2680: 2633: 2632: 2623: 2579: 2578: 2574: 2530: 2529: 2525: 2478: 2477: 2473: 2429: 2428: 2424: 2388: 2387: 2380: 2327: 2326: 2322: 2303:Cancer Research 2299: 2298: 2294: 2284: 2241: 2240: 2233: 2202: 2201: 2194: 2150: 2149: 2145: 2109: 2108: 2104: 2058: 2057: 2050: 2004: 2003: 1999: 1963: 1962: 1958: 1922: 1921: 1917: 1865: 1864: 1860: 1839:(12): 538–543. 1830: 1829: 1825: 1781: 1780: 1776: 1746: 1745: 1741: 1695: 1694: 1690: 1644: 1643: 1636: 1629: 1616: 1615: 1611: 1601: 1558: 1557: 1553: 1549: 1540:Mismatch repair 1530: 748:Function in NER 725: 716: 526: 513: 496: 454: 395: 389: 358: 335:side while the 306: 279: 250: 237: 212: 207: 127: 28: 23: 22: 15: 12: 11: 5: 3567: 3565: 3557: 3556: 3546: 3545: 3539: 3538: 3536: 3535: 3524: 3521: 3520: 3518: 3517: 3512: 3507: 3502: 3497: 3492: 3491: 3490: 3485: 3480: 3475: 3470: 3465: 3460: 3455: 3440: 3439: 3434: 3424: 3423: 3418: 3413: 3408: 3403: 3398: 3392: 3390: 3386: 3385: 3383: 3382: 3377: 3371: 3369: 3365: 3364: 3362: 3361: 3360: 3359: 3354: 3344: 3339: 3334: 3333: 3332: 3322: 3317: 3316: 3315: 3310: 3299: 3297: 3296:Other pathways 3293: 3292: 3290: 3289: 3284: 3279: 3274: 3269: 3268: 3267: 3257: 3252: 3246: 3244: 3238: 3237: 3235: 3234: 3233: 3232: 3227: 3217: 3216: 3215: 3210: 3205: 3200: 3195: 3190: 3185: 3180: 3175: 3170: 3165: 3160: 3146: 3145: 3144: 3139: 3134: 3119: 3117: 3111: 3110: 3105: 3103: 3102: 3095: 3088: 3080: 3074: 3073: 3059: 3058:External links 3056: 3054: 3053: 3024: 2989: 2945: 2939: 2925: 2923: 2920: 2918: 2917: 2876: 2827: 2796:(3): 1855–69. 2776: 2727: 2678: 2621: 2572: 2523: 2471: 2442:(7): 697–713. 2422: 2401:(24): 2886–8. 2378: 2320: 2292: 2231: 2192: 2143: 2116:Carcinogenesis 2102: 2048: 1997: 1976:(4): 599–603. 1970:Carcinogenesis 1956: 1915: 1858: 1823: 1794:(4): 250–258. 1774: 1755:(2): 233–252. 1739: 1688: 1634: 1627: 1609: 1550: 1548: 1545: 1544: 1543: 1537: 1529: 1526: 1523: 1522: 1517: 1514: 1511: 1506: 1501: 1490: 1489: 1484: 1481: 1478: 1473: 1468: 1457: 1456: 1451: 1448: 1445: 1440: 1435: 1424: 1423: 1412: 1409: 1406: 1395: 1386: 1375: 1374: 1369: 1366: 1363: 1358: 1353: 1342: 1341: 1336: 1333: 1330: 1325: 1320: 1309: 1308: 1303: 1300: 1297: 1292: 1287: 1276: 1275: 1270: 1267: 1264: 1259: 1254: 1243: 1242: 1237: 1234: 1231: 1226: 1221: 1210: 1209: 1204: 1201: 1198: 1193: 1188: 1177: 1176: 1171: 1170:Final ligation 1168: 1165: 1160: 1155: 1144: 1143: 1138: 1135: 1132: 1127: 1122: 1111: 1110: 1105: 1102: 1099: 1094: 1089: 1078: 1077: 1072: 1069: 1066: 1061: 1056: 1045: 1044: 1039: 1036: 1033: 1028: 1023: 1012: 1011: 1006: 1003: 1000: 995: 990: 979: 978: 973: 970: 967: 962: 957: 946: 945: 940: 937: 934: 929: 924: 913: 912: 907: 904: 901: 898: 893: 882: 881: 876: 873: 870: 867: 862: 851: 850: 845: 842: 839: 836: 831: 822: 821: 816: 813: 810: 805: 800: 789: 788: 783: 780: 777: 772: 767: 756: 755: 749: 746: 743: 737: 731: 724: 721: 715: 712: 638:Deficiency of 525: 522: 512: 509: 495: 492: 453: 450: 388: 385: 357: 354: 305: 302: 301: 300: 290: 278: 275: 267:RNA polymerase 249: 246: 245: 244: 236: 233: 211: 208: 206: 203: 126: 123: 100:DNA polymerase 96:thymine dimers 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 3566: 3555: 3552: 3551: 3549: 3534: 3526: 3525: 3522: 3516: 3513: 3511: 3508: 3506: 3503: 3501: 3498: 3496: 3493: 3489: 3486: 3484: 3481: 3479: 3476: 3474: 3471: 3469: 3466: 3464: 3461: 3459: 3456: 3454: 3451: 3450: 3449: 3445: 3444:FANC proteins 3442: 3441: 3438: 3435: 3433: 3429: 3426: 3425: 3422: 3419: 3417: 3414: 3412: 3409: 3407: 3404: 3402: 3399: 3397: 3394: 3393: 3391: 3387: 3381: 3378: 3376: 3373: 3372: 3370: 3366: 3358: 3355: 3353: 3350: 3349: 3348: 3345: 3343: 3340: 3338: 3335: 3331: 3328: 3327: 3326: 3323: 3321: 3318: 3314: 3311: 3309: 3306: 3305: 3304: 3301: 3300: 3298: 3294: 3288: 3285: 3283: 3280: 3278: 3275: 3273: 3270: 3266: 3265:RecQ helicase 3263: 3262: 3261: 3258: 3256: 3253: 3251: 3248: 3247: 3245: 3243: 3239: 3231: 3228: 3226: 3223: 3222: 3221: 3218: 3214: 3211: 3209: 3206: 3204: 3201: 3199: 3196: 3194: 3191: 3189: 3186: 3184: 3181: 3179: 3176: 3174: 3171: 3169: 3166: 3164: 3161: 3159: 3156: 3155: 3154: 3150: 3147: 3143: 3140: 3138: 3135: 3133: 3130: 3129: 3128: 3124: 3121: 3120: 3118: 3116: 3112: 3108: 3101: 3096: 3094: 3089: 3087: 3082: 3081: 3078: 3071: 3066: 3062: 3061: 3057: 3050: 3046: 3042: 3038: 3034: 3030: 3025: 3021: 3017: 3012: 3007: 3003: 2999: 2995: 2990: 2985: 2981: 2976: 2971: 2967: 2963: 2959: 2955: 2951: 2946: 2942: 2936: 2932: 2927: 2926: 2921: 2913: 2909: 2904: 2899: 2895: 2891: 2887: 2880: 2877: 2872: 2868: 2863: 2858: 2854: 2850: 2846: 2842: 2838: 2831: 2828: 2823: 2819: 2814: 2809: 2804: 2799: 2795: 2791: 2787: 2780: 2777: 2772: 2768: 2763: 2758: 2754: 2750: 2746: 2742: 2738: 2731: 2728: 2723: 2719: 2714: 2709: 2705: 2701: 2697: 2693: 2689: 2682: 2679: 2674: 2670: 2665: 2660: 2655: 2650: 2646: 2642: 2638: 2630: 2628: 2626: 2622: 2617: 2613: 2608: 2603: 2599: 2595: 2592:(7): 781–91. 2591: 2587: 2583: 2576: 2573: 2568: 2564: 2560: 2556: 2551: 2546: 2542: 2538: 2534: 2527: 2524: 2519: 2515: 2510: 2505: 2500: 2495: 2492:(2): 121–32. 2491: 2487: 2483: 2475: 2472: 2467: 2463: 2458: 2453: 2449: 2445: 2441: 2437: 2433: 2426: 2423: 2418: 2414: 2409: 2404: 2400: 2396: 2392: 2385: 2383: 2379: 2374: 2370: 2365: 2360: 2356: 2352: 2348: 2344: 2340: 2336: 2332: 2324: 2321: 2316: 2312: 2308: 2304: 2296: 2293: 2288: 2281: 2277: 2272: 2267: 2262: 2257: 2253: 2249: 2245: 2238: 2236: 2232: 2227: 2223: 2219: 2215: 2211: 2207: 2199: 2197: 2193: 2188: 2184: 2180: 2176: 2171: 2166: 2162: 2158: 2154: 2147: 2144: 2139: 2135: 2130: 2125: 2121: 2117: 2113: 2106: 2103: 2098: 2094: 2089: 2084: 2079: 2074: 2070: 2066: 2062: 2055: 2053: 2049: 2044: 2040: 2036: 2032: 2028: 2024: 2020: 2016: 2012: 2008: 2001: 1998: 1993: 1989: 1984: 1979: 1975: 1971: 1967: 1960: 1957: 1952: 1948: 1943: 1938: 1934: 1930: 1926: 1919: 1916: 1911: 1907: 1902: 1897: 1893: 1889: 1885: 1881: 1877: 1873: 1869: 1862: 1859: 1854: 1850: 1846: 1842: 1838: 1834: 1827: 1824: 1819: 1815: 1810: 1805: 1801: 1797: 1793: 1789: 1785: 1778: 1775: 1770: 1766: 1762: 1758: 1754: 1750: 1743: 1740: 1735: 1731: 1726: 1721: 1716: 1711: 1707: 1703: 1699: 1692: 1689: 1684: 1680: 1675: 1670: 1665: 1660: 1656: 1652: 1648: 1641: 1639: 1635: 1630: 1624: 1620: 1613: 1610: 1605: 1598: 1594: 1589: 1584: 1579: 1574: 1570: 1566: 1562: 1555: 1552: 1546: 1541: 1538: 1535: 1532: 1531: 1527: 1521: 1518: 1515: 1512: 1510: 1507: 1505: 1502: 1499: 1495: 1492: 1491: 1488: 1485: 1482: 1479: 1477: 1474: 1472: 1469: 1466: 1462: 1459: 1458: 1455: 1452: 1449: 1446: 1444: 1441: 1439: 1436: 1433: 1429: 1426: 1425: 1422: 1419: 1416: 1413: 1410: 1407: 1405: 1402: 1399: 1396: 1394: 1390: 1387: 1384: 1380: 1377: 1376: 1373: 1370: 1367: 1364: 1362: 1359: 1357: 1354: 1351: 1347: 1344: 1343: 1340: 1337: 1334: 1331: 1329: 1326: 1324: 1321: 1318: 1314: 1311: 1310: 1307: 1304: 1301: 1298: 1296: 1293: 1291: 1288: 1285: 1281: 1278: 1277: 1274: 1271: 1268: 1265: 1263: 1260: 1258: 1255: 1252: 1248: 1245: 1244: 1241: 1238: 1235: 1232: 1230: 1227: 1225: 1222: 1219: 1215: 1212: 1211: 1208: 1205: 1202: 1199: 1197: 1194: 1192: 1189: 1186: 1182: 1179: 1178: 1175: 1172: 1169: 1166: 1164: 1161: 1159: 1156: 1153: 1149: 1146: 1145: 1142: 1139: 1136: 1133: 1131: 1128: 1126: 1123: 1120: 1116: 1113: 1112: 1109: 1106: 1103: 1100: 1098: 1095: 1093: 1090: 1087: 1083: 1080: 1079: 1076: 1073: 1070: 1067: 1065: 1062: 1060: 1057: 1054: 1050: 1047: 1046: 1043: 1040: 1037: 1034: 1032: 1029: 1027: 1024: 1021: 1017: 1014: 1013: 1010: 1007: 1004: 1001: 999: 996: 994: 991: 988: 984: 981: 980: 977: 974: 971: 968: 966: 963: 961: 958: 955: 951: 948: 947: 944: 941: 938: 935: 933: 930: 928: 925: 922: 918: 915: 914: 911: 908: 905: 902: 899: 897: 894: 891: 887: 884: 883: 880: 877: 874: 871: 868: 866: 863: 860: 856: 853: 852: 849: 846: 843: 840: 837: 835: 832: 830: 827: 824: 823: 820: 817: 814: 811: 809: 806: 804: 801: 798: 794: 791: 790: 787: 784: 781: 778: 776: 773: 771: 768: 765: 761: 758: 757: 753: 750: 747: 744: 741: 738: 735: 732: 729: 728: 722: 720: 713: 711: 709: 705: 701: 697: 694: 690: 687: 682: 680: 676: 672: 668: 664: 660: 656: 652: 648: 643: 641: 636: 634: 630: 626: 621: 619: 615: 611: 607: 603: 599: 595: 591: 586: 584: 579: 577: 576: 571: 570: 565: 564: 559: 558: 553: 549: 545: 544: 539: 535: 531: 523: 521: 519: 510: 508: 505: 501: 493: 491: 488: 484: 479: 475: 471: 463: 458: 451: 449: 446: 442: 437: 435: 430: 426: 422: 418: 414: 410: 409: 399: 394: 386: 384: 382: 379: 375: 371: 367: 363: 355: 353: 350: 345: 342: 338: 334: 330: 326: 322: 318: 314: 310: 304:Dual incision 303: 298: 294: 291: 288: 285: 284: 283: 276: 274: 271: 268: 262: 254: 247: 242: 241: 240: 234: 232: 230: 226: 216: 209: 204: 202: 198: 196: 192: 188: 184: 180: 176: 172: 168: 164: 160: 156: 152: 148: 144: 140: 136: 132: 125:In eukaryotes 124: 122: 120: 116: 111: 109: 105: 101: 97: 93: 89: 84: 82: 78: 74: 70: 66: 62: 58: 54: 50: 46: 42: 34: 30: 19: 3447: 3428:DNA helicase 3411:8-Oxoguanine 3380:SOS response 3260:RecF pathway 3213:Excinuclease 3148: 3032: 3028: 3001: 2997: 2957: 2953: 2930: 2893: 2889: 2879: 2844: 2840: 2830: 2793: 2790:Biomolecules 2789: 2779: 2744: 2740: 2730: 2698:(1): 62–78. 2695: 2692:J. Mol. Biol 2691: 2681: 2644: 2640: 2589: 2585: 2575: 2540: 2536: 2526: 2489: 2485: 2474: 2439: 2435: 2425: 2398: 2394: 2338: 2334: 2323: 2306: 2302: 2295: 2251: 2247: 2209: 2205: 2160: 2156: 2146: 2119: 2115: 2105: 2071:(1): 47–55. 2068: 2064: 2010: 2006: 2000: 1973: 1969: 1959: 1932: 1928: 1918: 1875: 1871: 1861: 1836: 1832: 1826: 1791: 1787: 1777: 1752: 1748: 1742: 1705: 1701: 1691: 1654: 1650: 1618: 1612: 1568: 1565:PLOS Biology 1564: 1554: 1508: 1503: 1493: 1475: 1470: 1460: 1442: 1437: 1427: 1403: 1400: 1397: 1392: 1388: 1378: 1360: 1355: 1345: 1327: 1322: 1312: 1294: 1289: 1279: 1261: 1256: 1246: 1228: 1223: 1213: 1195: 1190: 1180: 1162: 1157: 1152:DNA Ligase I 1147: 1129: 1124: 1114: 1096: 1091: 1081: 1063: 1058: 1048: 1030: 1025: 1015: 997: 992: 982: 964: 959: 949: 931: 926: 916: 895: 885: 864: 854: 833: 825: 807: 802: 792: 774: 769: 759: 717: 707: 703: 699: 695: 683: 667:osteoporosis 658: 646: 644: 639: 637: 624: 622: 613: 589: 587: 582: 580: 573: 567: 561: 555: 547: 541: 533: 527: 514: 497: 483:phenotypical 467: 438: 433: 417:DNA helicase 406: 404: 370:DNA ligase I 364:) loads the 359: 346: 329:endonuclease 307: 280: 272: 263: 259: 238: 221: 199: 128: 112: 85: 40: 39: 29: 2486:Cancer Cell 1935:(1): 1–17. 1571:(6): e203. 829:(Centrin-2) 815:CAK subunit 518:lymphocytes 487:lung cancer 195:found below 161:, XPF, and 135:prokaryotes 92:DNA adducts 67:(BER), and 47:mechanism. 3554:DNA repair 3368:Regulation 3347:Photolyase 3107:DNA repair 3029:Mutat. Res 2741:Cell Cycle 2641:PLOS Genet 2537:Hum. Mutat 2509:10029/5565 2395:Cell Cycle 2248:BMC Cancer 1547:References 745:Subpathway 671:DNA damage 572:(CSB) and 478:DNA repair 462:DNA damage 441:TRCF (Mfd) 139:photolyase 131:eukaryotes 108:DNA ligase 81:base pairs 59:and other 45:DNA repair 3188:XPG/ERCC5 3173:XPD/ERCC2 2998:Mol. Cell 752:GeneCards 698:(CSA) or 689:mutations 57:radiation 3548:Category 3533:Category 3183:XPF/DDB1 3178:XPE/DDB1 3049:15913669 3020:12504014 2912:10877825 2871:17913742 2822:26287260 2771:24781187 2722:26616585 2673:25299392 2616:21612988 2567:22852219 2559:16947863 2518:16904611 2466:21571596 2417:17172862 2373:27556946 2315:11245433 2280:18267032 2226:12427537 2179:18196582 2138:15731165 2097:22754221 2043:22991719 2035:19492231 1992:11960912 1951:22493747 1910:23023028 1853:10562720 1818:19949546 1769:16464004 1734:20981145 1708:: 1–32. 1683:20725631 1657:: 1–10. 1597:16752948 1528:See also 896:Ddb2/Xpe 764:Cyclin H 742:Ortholog 736:Ortholog 686:germline 663:cachexia 635:(XPCS). 610:cachexia 297:progeria 61:mutagens 3375:SOS box 3127:AP site 2984:8836185 2890:FASEB J 2862:2190694 2813:4598778 2762:4111694 2713:4738086 2664:4191938 2607:3139823 2457:3234290 2364:5161687 2343:Bibcode 2271:2262891 2187:9456435 2088:3385179 2015:Bibcode 1942:3316453 1901:4586256 1880:Bibcode 1809:2709936 1725:2957137 1674:2915888 1588:1475692 900:Unknown 869:Unknown 838:Unknown 702:(CSB). 578:(CSA). 566:(XPG), 560:(XPF), 546:(XPD), 411:by the 376:or the 157:, XPD, 3500:FANCD2 3495:FANCD1 3255:RecBCD 3208:RAD23B 3203:RAD23A 3047:  3018:  2982:  2975:146147 2972:  2937:  2910:  2869:  2859:  2820:  2810:  2769:  2759:  2720:  2710:  2671:  2661:  2614:  2604:  2565:  2557:  2516:  2464:  2454:  2415:  2371:  2361:  2335:Nature 2313:  2278:  2268:  2254:: 50. 2224:  2185:  2177:  2136:  2095:  2085:  2041:  2033:  1990:  1949:  1939:  1908:  1898:  1851:  1816:  1806:  1767:  1732:  1722:  1681:  1671:  1625:  1595:  1585:  1447:TC-NER 1421:GTF2H3 1418:GTF2H2 1415:GTF2H1 1389:Gtf2h1 1306:RAD23B 1290:Rad23b 1284:RAD23B 1280:RAD23B 1273:RAD23A 1257:Rad23a 1251:RAD23A 1247:RAD23A 1134:TC-NER 1101:TC-NER 754:Entry 677:.(see 596:(XP), 470:cancer 452:Cancer 445:ATPase 434:E.coli 191:RAD23B 187:RAD23A 3515:FANCN 3510:FANCJ 3505:FANCI 3488:FANCM 3483:FANCL 3478:FANCG 3473:FANCF 3468:FANCE 3463:FANCC 3458:FANCB 3453:FANCA 3313:ERCC8 3308:ERCC6 3272:RAD51 3193:ERCC1 2563:S2CID 2183:S2CID 2039:S2CID 1542:(MMR) 1536:(BER) 1476:RAD14 1379:TFIIH 1295:RAD23 1262:RAD23 1240:MMS19 1229:MET18 1224:Mms19 1218:MMS19 1214:MMS19 1207:MNAT1 1191:Mnat1 1185:MNAT1 1181:MNAT1 1141:ERCC8 1130:RAD28 1125:Ercc8 1115:ERCC8 1108:ERCC6 1097:RAD26 1092:Ercc6 1082:ERCC6 1075:ERCC5 1059:Ercc5 1049:ERCC5 1042:ERCC4 1026:Ercc4 1016:ERCC4 1009:ERCC3 998:RAD25 993:Ercc3 983:ERCC3 976:ERCC2 960:Ercc2 950:ERCC2 943:ERCC1 932:RAD10 927:Ercc1 921:ERCC1 917:ERCC1 848:CETN2 834:Cetn2 826:CETN2 808:KIN28 740:Yeast 734:Mouse 708:ERCC6 704:ERCC8 700:ERCC6 696:ERCC8 693:genes 675:aging 659:ERCC5 647:ERCC5 640:ERCC4 625:ERCC3 614:ERCC2 590:ERCC2 583:ERCC1 575:ERCC8 569:ERCC6 563:ERCC5 557:ERCC4 548:ERCC3 543:ERCC2 538:ERCC1 534:ERCC1 524:Aging 425:dimer 341:ERCC1 179:ERCC1 133:than 43:is a 3401:PcrA 3357:CRY2 3352:CRY1 3287:LexA 3282:Slx4 3277:Sgs1 3250:RecA 3230:MSH2 3225:MLH1 3153:ERCC 3045:PMID 3016:PMID 2980:PMID 2935:ISBN 2908:PMID 2867:PMID 2818:PMID 2767:PMID 2718:PMID 2669:PMID 2612:PMID 2555:PMID 2514:PMID 2462:PMID 2413:PMID 2369:PMID 2311:PMID 2276:PMID 2222:PMID 2175:PMID 2134:PMID 2093:PMID 2031:PMID 1988:PMID 1947:PMID 1906:PMID 1849:PMID 1814:PMID 1765:PMID 1730:PMID 1706:2010 1679:PMID 1655:2010 1623:ISBN 1593:PMID 1509:RAD4 1480:Both 1454:XAB2 1443:SYF1 1438:Xab2 1432:XAB2 1428:XAB2 1408:Both 1404:Tfb4 1401:Ssl1 1398:Tfb1 1372:RPA2 1365:Both 1361:RFA2 1356:Rpa2 1350:RPA2 1346:RPA2 1339:RPA1 1332:Both 1328:RFA1 1323:Rpa1 1317:RPA1 1313:RPA1 1233:Both 1200:Both 1196:TFB3 1174:LIG1 1167:Both 1163:CDC9 1158:Lig1 1148:LIG1 1068:Both 1064:RAD2 1035:Both 1031:RAD1 1002:Both 969:Both 965:RAD3 936:Both 910:DDB2 890:DDB2 886:DDB2 879:DDB1 865:Ddb1 859:DDB1 855:DDB1 819:CDK7 812:Both 803:Cdk7 793:CDK7 786:CCNH 779:Both 775:CCL1 770:Ccnh 760:CCNH 673:and 665:and 502:and 381:seal 372:and 319:and 173:and 169:and 117:and 3437:WRN 3432:BLM 3396:Ogt 3198:RPA 3168:XPC 3163:XPB 3158:XPA 3037:doi 3033:577 3006:doi 2970:PMC 2962:doi 2898:doi 2857:PMC 2849:doi 2808:PMC 2798:doi 2757:PMC 2749:doi 2708:PMC 2700:doi 2696:428 2659:PMC 2649:doi 2602:PMC 2594:doi 2545:doi 2504:hdl 2494:doi 2452:PMC 2444:doi 2403:doi 2359:PMC 2351:doi 2339:537 2266:PMC 2256:doi 2214:doi 2210:509 2165:doi 2161:122 2124:doi 2083:PMC 2073:doi 2023:doi 1978:doi 1937:PMC 1896:PMC 1888:doi 1841:doi 1804:PMC 1796:doi 1757:doi 1753:106 1720:PMC 1710:doi 1669:PMC 1659:doi 1583:PMC 1573:doi 1520:XPC 1513:GGR 1504:Xpc 1498:XPC 1494:XPC 1487:XPA 1471:Xpa 1465:XPA 1461:XPA 1299:GGR 1266:GGR 1119:CSA 1086:CSB 1053:XPG 1020:XPF 987:XPB 954:XPD 903:GGR 872:GGR 841:GGR 681:). 620:). 554:), 552:XPB 540:), 504:XPC 500:XPD 362:RFC 349:XPA 337:XPF 321:XPB 317:XPD 313:XPG 229:XPE 225:XPC 183:RPA 175:CSB 171:CSA 163:XPG 159:XPE 155:XPC 151:XPB 147:XPA 55:), 49:DNA 3550:: 3446:: 3430:: 3330:Ku 3043:. 3031:. 3014:. 3002:10 3000:. 2996:. 2978:. 2968:. 2958:24 2956:. 2952:. 2906:. 2894:14 2892:. 2888:. 2865:. 2855:. 2845:35 2843:. 2839:. 2816:. 2806:. 2792:. 2788:. 2765:. 2755:. 2745:13 2743:. 2739:. 2716:. 2706:. 2694:. 2690:. 2667:. 2657:. 2645:10 2643:. 2639:. 2624:^ 2610:. 2600:. 2590:10 2588:. 2584:. 2561:. 2553:. 2541:27 2539:. 2535:. 2512:. 2502:. 2490:10 2488:. 2484:. 2460:. 2450:. 2440:10 2438:. 2434:. 2411:. 2397:. 2393:. 2381:^ 2367:. 2357:. 2349:. 2337:. 2333:. 2307:61 2305:. 2274:. 2264:. 2250:. 2246:. 2234:^ 2220:. 2208:. 2195:^ 2181:. 2173:. 2159:. 2155:. 2132:. 2120:26 2118:. 2114:. 2091:. 2081:. 2069:18 2067:. 2063:. 2051:^ 2037:. 2029:. 2021:. 2011:72 2009:. 1986:. 1974:23 1972:. 1968:. 1945:. 1931:. 1927:. 1904:. 1894:. 1886:. 1876:31 1874:. 1870:. 1847:. 1835:. 1812:. 1802:. 1792:10 1790:. 1786:. 1763:. 1751:. 1728:. 1718:. 1704:. 1700:. 1677:. 1667:. 1653:. 1649:. 1637:^ 1591:. 1581:. 1567:. 1563:. 333:3' 197:. 189:, 185:, 181:, 153:, 149:, 83:. 3151:/ 3125:/ 3099:e 3092:t 3085:v 3051:. 3039:: 3022:. 3008:: 2986:. 2964:: 2943:. 2914:. 2900:: 2873:. 2851:: 2824:. 2800:: 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Index

Transcription-coupled repair

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

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