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Mutagenesis by AID: Being in the Right Place at the Right Time

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Vyšlo v časopise: Mutagenesis by AID: Being in the Right Place at the Right Time. PLoS Genet 11(9): e32767. doi:10.1371/journal.pgen.1005489
Kategorie: Perspective
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1005489

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Zdroje

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2. Le Q, Maizels N. Cell Cycle Regulates Nuclear Stability of AID and Determines the Cellular Response to AID. PLoS Genet.

3. Taylor BJ, Nik-Zainal S, Wu YL, Stebbings LA, Raine K, Campbell PJ, et al. DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis. Elife. 2013 Apr 16;2:e00534. doi: 10.7554/eLife.00534 23599896

4. Alexandrov LB, Nik-Zainal S, Wedge DC, Aparicio SAJR, Behjati S, Biankin AV, et al. Signatures of mutational processes in human cancer. Nature. 2013;500:415–421. doi: 10.1038/nature12477 23945592

5. Pettersen HS, Galashevskaya A, Doseth B, Sousa MML, Sarno A, Visnes T, et al. AID expression in B-cell lymphomas causes accumulation of genomic uracil and a distinct AID mutational signature. DNA Repair (Amst). 2015;25:60–71.

6. Orthwein A, Di Noia JM. Activation induced deaminase: how much and where? Seminars in Immunology. 2012;24:246–254. doi: 10.1016/j.smim.2012.05.001 22687198

7. Faili A, Aoufouchi S, Guéranger Q, Zober C, Léon A, Bertocci B, et al. AID-dependent somatic hypermutation occurs as a DNA single-strand event in the BL2 cell line. Nat Immunol. 2002;3: 815–821. 12145648

8. Sharbeen G, Yee CWY, Smith AL, Jolly CJ. Ectopic restriction of DNA repair reveals that UNG2 excises AID-induced uracils predominantly or exclusively during G1 phase. J Exp Med. 2012;209: 965–974. doi: 10.1084/jem.20112379 22529268

9. Peña-Diaz J, Jiricny J. Mammalian mismatch repair: error-free or error-prone? Trends Biochem Sci. 2012;37: 206–214. doi: 10.1016/j.tibs.2012.03.001 22475811

10. Häsler J, Rada C, Neuberger MS. The cytoplasmic AID complex. Seminars in Immunology. 2012;24:273–280. doi: 10.1016/j.smim.2012.05.004 22698843

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Článok vyšiel v časopise

PLOS Genetics

2015 Číslo 9

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Autori: MUDr. Tomáš Ürge, PhD.

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