DNA-(apurinic or apyrimidinic site) lyase

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DNA-(apurinic or apyrimidinic site) lyase
DNA AP Lyase.png
Structure of APE1 DNA AP Lyase bound to DNA, generated from 1DE9[1]
EC number
CAS number 61811-29-8
IntEnz IntEnz view
ExPASy NiceZyme view
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Gene Ontology AmiGO / EGO

In enzymology, DNA-(apurinic or apyrimidinic site) lyase, also referred to as DNA-(apurinic or apyrimidinic site) 5'-phosphomonoester-lyase (systematic name) or DNA AP lyase (EC is a class of enzyme that catalyzes the chemical reaction of the cleavage of the C3'-O-P bond 3' from the apurinic or apyrimidinic site in DNA via beta-elimination reaction, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate.[2] In the 1970s, this class of enzyme was found to repair at apurinic or apyrimidinic DNA sites in E. coli and in mammalian cells. The major active enzymes of this class in bacteria, and specifically, E. coli is endonuclease type III, while in humans it is a Mg2+-dependent AP endonuclease, APE1.[3][4] This enzyme encompasses a family of lyases that cleave carbon-oxygen bonds.

Several names for DNA AP lyase include: AP lyase; AP endonuclease class I; endodeoxyribonuclease (apurinic or apyrimidinic); deoxyribonuclease (apurinic or apyrimidinic); E. coli endonuclease III; phage-T4 UV endonuclease; Micrococcus luteus UV endonuclease; AP site-DNA 5'-phosphomonoester-lyase; and X-ray endonuclease III.

Structural Studies[edit]

Since DNA AP lyase is a class of structures who have numerous target genes that encode for different variations of the enzyme, there is no one single enzyme structure that can be used as an example that encompasses all versions of the enzyme. As of March 2015, 99 structures have been solved for this class of enzymes, including 23 PDB accession codes 1BIX, 1CQG, 1CQH, 1DE8, 1DE9, 1DEW, 1E9N, 1HD7, 1N39, 1N3A, 1N3C, 1VYB, 2ABK, 2I5W, 2ISI, 2J63, 2NOB, 2NOE, 2NOF, 2NOH, 2NOI, 2NOL, and 2NOZ. APE1 is a gene that codes for DNA AP lyase in humans which binds to AP DNA loops into both the DNA major and minor grooves and binds a flipped-out AP site in a pocket that excludes DNA bases and racemized-anomer AP sites. Both the APE1 active-site geometry and a complex with cleaved AP-DNA and Mn2+ support a testable structure-based catalytic mechanism. Mn2+ stabilizes the reaction of the lyase activity.[4]


AP lyase enzymes catalyze reactions analogous to β-elimination reaction. Initially, AP hydrolyses, such as apurinic or apyrimidinic endonuclease I contain a Mg2+ active site that cleaves the DNA on the 5'-side, yielding a 5'-deoxyribosephosphate and 3'-OH.[5] An AP site in DNA appears when the glycosylic bond that connects the purine or pyrimidine base to the deoxyribose sugar is cleaved.[6] This reaction is referred to as depurination or depyrimidination. The sugar at the AP site is a highly unstable cyclic carboxonium ion that undergoes rapid hydrolysis to yield a diastereomeric mixture of 2-deoxy-α-D-ribose and 2-deoxy-β-D-ribose. AP lyase enzymes could be trapped on both pre-incised and unincised AP DNA by a reducing agent such as sodium borohydride. Furthermore, the catalytic mechanism of AP lyases, the β-elimination reaction, proceeds through an imine enzyme–DNA intermediate.[7]

AP lyase mechanism.[5] AP lyase, in blue, catalyzes the second reaction.

Biological Function[edit]

In E. coli, DNA AP lyase (endonuclease III) helps repair oxidative damage to DNA bases by catalyzing the excision of the damaged pyrimidines and purines from ring saturation or opening from the DNA backbone. This damage can be caused by non-enzymatic hydrolysis, and/or exposure to ionizing radiation.[8][9]

Both UV endonuclease V from bacteriophage T4 (UV endonuclease V) and UV endonuclease III from E. coli catalyze N- glycosylase and the 3‘-abasic endonuclease reactions. Bacteriophage T4 and Micrococcus luteus UV endonucleases were actually shown not to be under the class of "endonuclease," but rather were β-elimination catalysts for reactions at AP sites at the C3'-O-P bond—thus, classifying them as AP lyases. Phage-T4 UV endonucleases also catalyze the reaction of the δ-reaction, nicking C5'-O-P bond at AP sites, although this reaction is slow and the enzyme should still be classified as AP lyase. This open ring allows the substitution of the correct base by other enzymes.[10][11][12]

DNA AP lyase activity is documented to have similar function in both E. Coli and in humans. A homolog of endonuclease III, human endonuclease III homolog 1, or hNTH1 functions similarly in humans as its homolog does in E. Coli.[13]

Disease Relevance[edit]

DNA damage is ubiquitous amongst all forms of life. There is an estimated 1 x 10−4 to 1 x 10−6 mutations per human gamete, which follows to finding at least one mutation at a specific locus per one million gametes.[14] DNA is the only biologic molecule that relies solely on repair of existing molecules, and is the largest molecule that can continue to function albeit numerous mutations; thus, mutations accumulate over time.[15] However without this repair, conditions such as UV-sensitive syndrome,[16] xeroderma pigmentosum,[17] and Cockayne syndrome[15] may arise.


The least severe of the three, people suffering from UV-sensitive syndrome experience UV-hypersensitivity. The syndrome arises from a mutation in the KIAA1530 protein. Unlike other severe conditions involving skin cancers and significantly reduced lifespan,[18] this condition may result in freckles, and other skin blemishes, but does not increase likelihood of attracting a skin cancer.[19] This condition is so rare that it has been documented to occur in seven individuals[20] worldwide. However, it is speculated that this condition is understudied, and there are, in fact, more individuals living with the syndrome.

Xeroderma pigmentosum or XP is a rare genetic disorder that occurs worldwide. On affected people, exposure to UV radiation, especially from the sun is limited and solar pigmentations and xerosis occur. The affected may loose eyebrows, become bloodshot in the eyes, and in extreme, untreated cases, may result in extreme photo-damage resulting in skin cancers and decreased lifespan due to metastatic malignant melanoma and squamous cell carcinoma.[21] However, some studies report that experimental treatments with repair enzyme T4 endonuclease V[22] and oral isotretinoin may be useful in preventing skin cancer acquired from the disorder.[23][24]

If transcription-coupled repair is lost, it has little effect on mutagenesis; however, this has severe implications on progeroid syndromes, especially in genes encoding CSA and CSB proteins. Mutations in these genes cause Cockayne Syndrome, which is characterized by early cessation of growth and development, leading to severe and progressive neurodysfunction associated with demyelination, sensorineural hearing loss, cataracts, cachexia, and frailty.[15] The average lifespan of patients with the disease is 12 years.[18] For CS Type II patients who have little neural growth after birth, the lifespan is significantly decreased to 7 years after birth. This condition can occur alongside xeroderma pigmentosum, resulting in xeroderma pigmentosum-cockayne syndrome (XP-CS).

See also[edit]


  1. ^ Mol, C. D.; Izumi, T; Mitra, S; Tainer, J. A. (2000). "DNA-bound structures and mutants reveal abasic DNA binding by APE1 and DNA repair coordination corrected". Nature 403 (6768): 451–6. doi:10.1038/35000249. PMID 10667800.  edit
  2. ^ "Homo sapiens GO:0003906 - DNA-(apurinic or apyrimidinic site) lyase activity". HumanCyc. SRI International. Retrieved March 9, 2015. 
  3. ^ Bailly, V; Verly, W. G. (1989). "AP endonucleases and AP lyases". Nucleic acids research 17 (9): 3617–8. PMC 317828. PMID 2471157.  edit
  4. ^ a b Errol C. Friedberg; Graham C. Walker; Wolfram Siede; Richard D. Wood (22 November 2005). DNA Repair and Mutagenesis. American Society for Microbiology Press. pp. 511–512. ISBN 978-1-55581-319-2. 
  5. ^ a b Müller TA, Andrzejak MM, Hausinger RP (2013). "A covalent protein-DNA 5'-product adduct is generated following AP lyase activity of human ALKBH1 (AlkB homologue 1).". Biochem J 452 (3): 509–18. doi:10.1042/BJ20121908. PMC 4126167. PMID 23577621. 
  6. ^ Loeb, L. A.; Preston, B. D. (1986). "Mutagenesis by apurinic/apyrimidinic sites". Annual Review of Genetics 20: 201–30. doi:10.1146/annurev.ge.20.120186.001221. PMID 3545059.  edit
  7. ^ Piersen CE, McCullough AK, Lloyd RS (2000). "AP lyases and dRPases: commonality of mechanism.". Mutat Res 459 (1): 43–53. doi:10.1016/s0921-8777(99)00054-3. PMID 10677682. 
  8. ^ Lindahl, T; Nyberg, B (1972). "Rate of depurination of native deoxyribonucleic acid". Biochemistry 11 (19): 3610–8. PMID 4626532.  edit
  9. ^ Verly, W. G. (1982). "Repair of AP sites in DNA". Biochimie 64 (8-9): 603–5. PMID 6814509.  edit
  10. ^ Manoharan, Muthiah.; Mazumder, Abhijit.; Ransom, Stephen C.; Gerlt, John A.; Bolton, Philip H. (1988). "Mechanism of UV endonuclease-V cleavage of abasic sites in DNA determined by C-13 labeling". J. Am. Chem. Soc. (American Chemical Society (ACS) 110 (8): 2690–2691. doi:10.1021/ja00216a074. Retrieved 10 March 2015. 
  11. ^ Bailly, V; Sente, B; Verly, W. G. (1989). "Bacteriophage-T4 and Micrococcus luteus UV endonucleases are not endonucleases but beta-elimination and sometimes beta delta-elimination catalysts". The Biochemical journal 259 (3): 751–9. PMC 1138582. PMID 2471512.  edit
  12. ^ Bailly, V; Verly, W. G. (1987). "Escherichia coli endonuclease III is not an endonuclease but a beta-elimination catalyst". The Biochemical journal 242 (2): 565–72. PMC 1147742. PMID 2439070.  edit
  13. ^ Aspinwall, R; Rothwell, D. G.; Roldan-Arjona, T; Anselmino, C; Ward, C. J.; Cheadle, J. P.; Sampson, J. R.; Lindahl, T; Harris, P. C.; Hickson, I. D. (1997). "Cloning and characterization of a functional human homolog of Escherichia coli endonuclease III". Proceedings of the National Academy of Sciences of the United States of America 94 (1): 109–14. PMC 19249. PMID 8990169.  edit
  14. ^ Clancy, Suzanne (2008). "DNA damage & repair: mechanisms for maintaining DNA integrity". Nature Education 1 (1): 103. Retrieved March 8, 2015. 
  15. ^ a b c Hoeijmakers, J. H. (2009). "DNA damage, aging, and cancer". New England Journal of Medicine 361 (15): 1475–85. doi:10.1056/NEJMra0804615. PMID 19812404.  edit
  16. ^ Schwertman, P; Vermeulen, W; Marteijn, J. A. (2013). "UVSSA and USP7, a new couple in transcription-coupled DNA repair". Chromosoma 122 (4): 275–84. doi:10.1007/s00412-013-0420-2. PMC 3714559. PMID 23760561.  edit
  17. ^ Halpern, J.; Hopping, B.; Brostoff, J. (2008). "Photosensitivity, corneal scarring and developmental delay: Xeroderma Pigmentosum in a tropical country". Cases journal 1 (1): 254. doi:10.1186/1757-1626-1-254. PMC 2577106. PMID 18937855. 
  18. ^ a b Andressoo, J. O.; Hoeijmakers, J. H. (2005). "Transcription-coupled repair and premature ageing". Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 577 (1-2): 179–94. doi:10.1016/j.mrfmmm.2005.04.004. PMID 16009385.  edit
  19. ^ "UV-Sensitive Syndrome". Genetics Home Reference. Retrieved 10 March 2015. 
  20. ^ "DNA Repair Disorders". Geneskin. Retrieved 10 March 2015. 
  21. ^ Li, Lei (January 8, 2007). "Chapter 3 Nucleotide Excision Repair". DNA REPAIR, GENETIC INSTABILITY, AND CANCER. World Scientific Publishing. pp. 75–76. ISBN 981-270-014-5. 
  22. ^ Yarosh, D; Klein, J; O'Connor, A; Hawk, J; Rafal, E; Wolf, P (2001). "Effect of topically applied T4 endonuclease V in liposomes on skin cancer in xeroderma pigmentosum: A randomised study. Xeroderma Pigmentosum Study Group". Lancet 357 (9260): 926–9. PMID 11289350.  edit
  23. ^ Kraemer, K. H.; Digiovanna, J. J.; Moshell, A. N.; Tarone, R. E.; Peck, G. L. (1988). "Prevention of skin cancer in xeroderma pigmentosum with the use of oral isotretinoin". New England Journal of Medicine 318 (25): 1633–7. doi:10.1056/NEJM198806233182501. PMID 3287161.  edit
  24. ^ Bath-Hextall F, Leonardi-Bee J, Somchand N, Webster A, Delitt J, Perkins W (2007). "Interventions for preventing non-melanoma skin cancers in high-risk groups.". Cochrane Database Syst Rev (4): CD005414. doi:10.1002/14651858.CD005414.pub2. PMID 17943854. 

Further reading[edit]