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DNA polymerase η is an A-T mutator in somatic hypermutation of immunoglobulin variable genes
Abstract
To determine whether DNA polymerase eta plays a role in the hypermutation of immunoglobulin variable genes, we examined the frequency and pattern of substitutions in variable VH6 genes from the peripheral blood lymphocytes of three patients with xeroderma pigmentosum variant disease, whose polymerase eta had genetic defects. The frequency of mutation was normal but the types of base changes were different: there was a decrease in mutations at A and T and a concomitant rise in mutations at G and C. We propose that more than one polymerase contributes to hypermutation and that if one is absent, others compensate. The data indicate that polymerase eta is involved in generating errors that occur predominantly at A and T and that another polymerase(s) may preferentially generate errors opposite G and C.
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“is characterized by a pattern of mutations that has been attributed to pol h (see the Discussion section for details) recruited for the repair of DNA damaged by AID during somatic hypermutation in immunoglobulin genes [28][29][30] .”
From DNA polymerase η mutational signatures are found in a variety of different types of cancer (2018) · cites this paper as [30]
Citations
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Items 201–300 of 420
Aid and Apobec Deaminases: Balancing Dna Damage in Epigenetics and Immunity
Franchini, D., & Petersen‐Mahrt, S. K. (2014) · Epigenomics · doi:10.2217/epi.14.35 · Cited by 31
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“The sequence context of in vivo IGV mutations from A and T has been compared favorably with that shown by mutations caused by Pol when copying a lac Z gene, or a mouse transgene in vitro (16–18), and Pol -deficient mice and humans show a reduced level of mutation from A and T (14, 15, 26, 27).”
BackgroundMethodDown-regulation of DNA polymerase β accompanies somatic hypermutation in human BL2 cell lines
Poltoratsky, V. P., Prasad, R., Horton, J. K., & Wilson, S. H. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.10.003 · Cited by 32
“Studies of mouse models have shown that pol β is not required for SHM [8], while other polymerases appeared to be responsible [9,10].”
BackgroundSomatic hypermutation: subverted DNA repair
Martomo, S. A., & Gearhart, P. J. (2006) · Current Opinion in Immunology · doi:10.1016/j.coi.2006.03.007 · Cited by 32
Self-citationActivation-induced cytidine deaminase-mediated hypermutation in the DT40 cell line
Arakawa, H., & Buerstedde, J.-M. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0202 · Cited by 31
“In the mouse, Polh seems to be responsible for mutations at A/T bases, since Polh-deficient B cells lack most of these mutations (Zeng et al. 2001).”
BackgroundMultifaceted activities of DNA polymerase η: beyond translesion DNA synthesis
Acharya, N., Kodavati, M. M., Peroumal, D., Khandagale, P., Patel, S. K., Sahu, S. R., & Kumari, P. (2018) · Current Genetics · doi:10.1007/s00294-018-0918-5 · Cited by 31
Immunoglobulin gene rearrangement, repertoire diversity, and the allergic response
Collins, A. M., Sewell, W. A., & Edwards, M. R. (2003) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2003.07.002 · Cited by 31
Competitive repair pathways in immunoglobulin gene hypermutation
Reynaud, C., Delbos, F., Faili, A., Guéranger, Q., Aoufouchi, S., & Weill, J. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0206 · Cited by 31
“The second activity characterized as being involved in A/T mutagenesis was Polh, a then recently discovered translesion DNA synthesis (TLS) polymerase, through the analysis of patients with the variant form of the xeroderma pigmentosum syndrome (XPV), a genetic disease corresponding to the dysfunction of this enzyme (…”
BackgroundAID function in somatic hypermutation and class switch recombination
Yu, K. (2022) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2022070 · Cited by 30
“MMR in germinal center B cells deviates from its canonical form by using error-prone DNA polymerases, primarily polymerase eta, during the gap filling step [23,24].”
BackgroundAnanda, G., Hile, S. E., Breski, A., Wang, Y., Kelkar, Y., Makova, K. D., & Eckert, K. A. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004498 · Cited by 29
“On the other hand, Pol g performs a key role in targeted mutagenesis during somatic hypermutation of immunoglobulin genes, primarily targeting mutations to A:T basepairs [69–71].”
BackgroundMeroni, A., Nava, G. M., Bianco, E., Grasso, L., Galati, E., Bosio, M. C., Delmastro, D., Muzi-Falconi, M., & Lazzaro, F. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz165 · Cited by 29
Vaisman, A., Lehmann, A. R., & Woodgate, R. (2004) · Advances in protein chemistry · doi:10.1016/s0065-3233(04)69007-3 · Cited by 30
Self-citationSantiago, M. J., Alejandre-Durán, E., & Ruiz‐Rubio, M. (2006) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2006.05.036 · Cited by 30
Tsao, W.-C., & Eckert, K. A. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103255 · Cited by 32
“Furthermore, Pol η has roles in additional cellular processes, including mismatch repair [97], homologous recombination [98], and somatic hypermutation [99].”
BackgroundHijacked DNA repair proteins and unchained DNA polymerases
Saribasak, H., Rajagopal, D., Maul, R. W., et al. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0188 · Cited by 28
“Third, U could be recognized as a U:G mismatch by the MSH2–MSH6 mismatch repair (MMR) proteins, which would generate a gap that could be filled in by the low-fidelity DNA polymerase (pol) h to produce mutations of A:T base pairs (bp; Zeng et al. 2001; Wilson et al. 2005).”
BackgroundInfluentialSelf-citationSale, J. E., Batters, C., Edmunds, C. E., Phillips, L. G., Simpson, L. J., & Szüts, D. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0197 · Cited by 29
“Numerous lines of evidence point to a central role for DNA polymerase h (Zeng et al. 2001; Delbos et al. 2005).”
BackgroundSteele, E. J., Franklin, A., & Blanden, R. V. (2004) · Immunology and Cell Biology · doi:10.1046/j.0818-9641.2004.01224.x · Cited by 27
“Data adapted from Zeng et al. (2001).55 Rearranged VH6 genes isolated using two step nested PCR (2 × 30 temperature cycles) as in Rosner et al.”
MethodXiao, Z., Ray, M., Jiang, C., Clark, A. B., Rogozin, I. B., & Diaz, M. (2007) · Molecular Immunology · doi:10.1016/j.molimm.2006.12.006 · Cited by 28
“…synthesis (TLS) DNA polymerases such as DNA polymerase η, ζ, θ, and ι (Diaz and Lawrence 2005, Zan et al., 2005, Delbos et al., 2005, Mayorov et al., 2005, Faili et al., 2002a, Diaz et al., 2001, Rogozin et al., 2001, Zan et al., 2001, Zeng et al., 2001), however, this model remains speculative.”
BackgroundSteele, E. J. (2016) · DNA repair · doi:10.1016/j.dnarep.2016.07.001 · Cited by 28
“DNA polymerase- the A/T mutator is a reverse ranscriptase In 2004 Andrew Franklin discovered [37] that the human A/T utator in SHM, DNA Polymerase- [57], was an efficient reverse ranscriptase in assays in vitro.”
SAMHD1 enhances immunoglobulin hypermutation by promoting transversion mutation
Thientosapol, E. S., Bosnjak, D., Durack, T., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1719771115 · Cited by 27
Related Mechanisms of Antibody Somatic Hypermutation and Class Switch Recombination
Hwang, J. K., Alt, F. W., & Yeap, L.-S. (2015) · ASM Press eBooks · doi:10.1128/9781555819217.ch15 · Cited by 29
Mismatch-mediated error prone repair at the immunoglobulin genes
Chahwan, R., Edelmann, W., Scharff, M. D., & Roa, S. (2011) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2011.09.001 · Cited by 28
“In mice and humans deficient in Polη, mutations in A:T bases are greatly reduced, indicating that it is the major translesional error prone polymerase recruited to antibody V regions by MMR [66,118,119,120].”
BackgroundRestricting activation‐induced cytidine deaminase tumorigenic activity in B lymphocytes
Casellas, R. C., Yamane, A., Kovalchuk, A. L., et al. (2008) · Immunology · doi:10.1111/j.1365-2567.2008.03050.x · Cited by 26
Error-Prone DNA Repair Activity during Somatic Hypermutation in Shark B Lymphocytes
Zhu, C. Y., & Hsu, E. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000779 · Cited by 26
Maul, R. W., MacCarthy, T., Frank, E. G., Donigan, K. A., McLenigan, M. P., Yang, W. W., Saribasak, H., Huston, D., Lange, S. S., Woodgate, R., et al. (2016) · The Journal of Experimental Medicine · doi:10.1084/jem.20151227 · Cited by 26
“Pol η is responsible for the majority of mutations of A:T bp (Zeng et al., 2001; Delbos et al., 2007), and Pol ζ contributes to synthesis of tandem double mutations (Daly et al.”
BackgroundSelf-citationZubani, G. G., Zivojnovic, M., Smet, A. D., Albagli, O., Huetz, F., Weill, J., Reynaud, C., & Storck, S. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20161576 · Cited by 26
“In contrast, mutations at A-T base pairs are introduced during an error-prone gap filling by DNA polymerase η (Zeng et al., 2001; Delbos et al., 2007), after its recruitment by monoubiquitinated proliferating cell nuclear antigen (PCNA; Langerak et al., 2007).”
BackgroundA role for Mlh3 in somatic hypermutation
Li, Z., Peled, J. U., Zhao, C., Svetlanov, A., Ronai, D., Cohen, P. E., & Scharff, M. D. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.02.003 · Cited by 26
Biological functions of translesion synthesis proteins in vertebrates
Jansen, J. G. (2003) · DNA repair · doi:10.1016/s1568-7864(03)00119-8 · Cited by 26
A high-resolution landscape of mutations in the BCL6 super-enhancer in normal human B cells
Shen, J.-C., Kamath‐Loeb, A. S., Kohrn, B. F., Loeb, K. R., Preston, B. D., & Loeb, L. A. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1914163116 · Cited by 24
Ohm‐Laursen, L., & Barington, T. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.7.4322 · Cited by 25
“Pol -deficient mice and patients with variant xeroderma pigmentosum who have a mutation in the gene encoding pol display a reduced level of A/T substitution despite a normal overall mutation rate (29, 31, 54).”
BackgroundBarnes, R. P., & Eckert, K. A. (2017) · Genes · doi:10.3390/genes8010019 · Cited by 26
“Eta (η) POLH Translesion synthesis [3] Common Fragile Site stability [14] DNA repair synthesis (MMR; HR) [31,32] Somatic Hypermutation [33]”
BackgroundSomatic hypermutation targeting is influenced by location within the immunoglobulin V region
Magori‐Cohen, R., Kleinstein, S. H., & Louzoun, Y. (2011) · Molecular Immunology · doi:10.1016/j.molimm.2011.04.002 · Cited by 24
“AID targets specific locations in the Ig gene [12–14].”
BackgroundExpression of AID transgene is regulated in activated B cells but not in resting B cells and kidney
Shen, H. M., Bozek, G., Pinkert, C. A., et al. (2007) · Molecular Immunology · doi:10.1016/j.molimm.2007.10.041 · Cited by 24
“PreB cells also express several factors (Hoffmann et al., 2002) that are present in replicating PNAhi cells and known to be important for SHM: e.g. lesion bypass polymerases (Zeng et al., 2001), Ung (Di Noia et al., 2006; Rada et al., 2002) and Msh2 (Marra et al., 1996).”
BackgroundTherapeutic Control of Hepatitis C Virus: The Role of Neutralizing Monoclonal Antibodies
Machida, K., Keck, Z., Lai, M. M. C., et al. (2007) · Current topics in microbiology and immunology · doi:10.1007/978-3-540-72146-8_1 · Cited by 24
“Among the latter, Pol ι, Pol η, and Pol ζ are involved in these pathways (Zan et al. 2001; Zeng et al. 2001; Faili et al. 2002).”
BackgroundBiochemical analysis of active site mutations of human polymerase η
Suarez, S. C., Beardslee, R. A., Toffton, S. M., & McCulloch, S. D. (2013) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2013.03.001 · Cited by 22
Human DNA polymerase mu (Pol micro) exhibits an unusual replication slippage ability at AAF lesion
Duvauchelle, J.-B. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.9.2061 · Cited by 23
“However, recent data indicate that a combination of several error-prone DNA polymerases might contribute to this process: Pol ζ (8), Pol η and Pol κ (9, 10 ) as well as Pol ι (11) are potential candidates (for a review on new eucaryotic DNA polymerase, see ref.”
BackgroundThe role of activation-induced deaminase in antibody diversification and genomic instability
Wang, J. H. (2012) · Immunologic Research · doi:10.1007/s12026-012-8369-4 · Cited by 22
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“…of bypassing other DNA lesions (8-oxoguanine, cisplatin, AP sites) [Haracska et al., 2000, 2001b; Masutani et al., 2000; Vaisman et al., 2000; Zhao et al., 2004; Prakash et al., 2005] and is moreover involved in homologous recombination [Kawamoto et al., 2005; McIlwraith et al., 2005;…”
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Steele, E. J., & Lindley, R. A. (2017) · DNA repair · doi:10.1016/j.dnarep.2017.04.004 · Cited by 21
AID Biology: A pathological and clinical perspective
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Self-citationHao, Q., Zhan, C., Lian, C., Luo, S., Cao, W., Wang, B., Xie, X., Ye, X., Gui, T., Voena, C., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.ade1167 · Cited by 21
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“Such thinking was vindicated by the discovery of decreased antibody hypermutation at A:T pairs in human patients deficient in DNA polymerase (51).”
BackgroundGerminal Center Function in the Spleen during Simian HIV Infection in Rhesus Monkeys
Margolin, D. H., Saunders, E. F. H., Bronfin, B., et al. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.2.1108 · Cited by 20
Sequence-specific targeting of two bases on both DNA strands by the somatic hypermutation mechanism
Shapiro, G. (2003) · Molecular Immunology · doi:10.1016/s0161-5890(03)00101-9 · Cited by 20
Temporal Regulation of Ig Gene Diversification Revealed by Single-Cell Imaging
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“The repair polymerase, Polη, participates in both gene conversion (29,30) and somatic hypermutation (31-35), and can generate the templated mutations characteristic of normally proliferating chicken B cells.”
DNA polymerase eta is regulated by poly(rC)-binding protein 1 via mRNA stability
Ren, C., Cho, S.-J., Jung, Y.-S., & Chen, X.-B. (2014) · Biochemical Journal · doi:10.1042/bj20141164 · Cited by 17
Ig gene hypermutation: A mechanism is due
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Normal Somatic Hypermutation of Ig Genes in the Absence of 8-Hydroxyguanine-DNA Glycosylase
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“DNA polymerase has been proposed to be an A:T mutator, because humans without the polymerase have fewer mutations of A and T (45, 46).”
BackgroundSelf-citationProbing DNA Base-Dependent Leaving Group Kinetic Effects on the DNA Polymerase Transition State
Oertell, K., Kashemirov, B. A., Negahbani, A., Minard, C., Haratipour, P., Alnajjar, K. S., Sweasy, J. B., Batra, V. K., Beard, W. A., Wilson, S. H., et al. (2018) · Biochemistry · doi:10.1021/acs.biochem.8b00417 · Cited by 19
Translesion DNA Synthesis and Carcinogenesis
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Molecular mechanisms in allergy and clinical immunology
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Mechanisms regulating the targeting and activity of activation induced cytidine deaminase
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“Here, bases surrounding the initial dU lesion are removed [14] and replaced in an error-prone manner through the action of DNA Pol h (POL H [15]) and Pol z (Pol Z or REV3L [14]), spreading mutations to the surrounding base pairs (reviewed in [13]).”
BackgroundDNA damage pathways and B-cell lymphomagenesis
Knittel, G., Rehkämper, T., Nieper, P., Schmitt, A., Flümann, R., & Reinhardt, H. C. (2018) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000433 · Cited by 18
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Refining the Neuberger model: Uracil processing by activated B cells
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Self-citationComputational analysis of mutation spectra
Rogozin, I. B. (2003) · Briefings in Bioinformatics · doi:10.1093/bib/4.3.210 · Cited by 17
A/T-targeted somatic hypermutation: critique of the mainstream model
Franklin, A., & Blanden, R. V. (2006) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2006.03.008 · Cited by 17
Molecular Mechanism of Class Switch Recombination
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ADAR1 Protein Induces Adenosine-targeted DNA Mutations in Senescent Bcl6 Gene-deficient Cells
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“Thus, this detectable ADAR1 in GC B cells may be involved in A-T targeted SHM, including a suite of DNA repair polymerases and enzymes led by an A-T mutator, DNA polymerase- (51, 52).”
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Hypermutation at A/T Sites during G·U Mismatch Repair in Vitro by Human B-cell Lysates
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ATAD5 Deficiency Decreases B Cell Division and Igh Recombination
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The mismatch repair pathway functions normally at a non-AID target in germinal center B cells
Green, B., Belcheva, A., Nepal, R. M., Boulianne, B., & Martín, A. (2011) · Blood · doi:10.1182/blood-2011-03-345991 · Cited by 15
Masuda, K., Ouchida, R., Yokoi, M., Hanaoka, F., Azuma, T., & Wang, J. O. (2008) · European Journal of Immunology · doi:10.1002/eji.200838502 · Cited by 14
KOMORI, A., XU, Z., WU, X., Zan, H., & Casali, P. (2006) · Molecular Immunology · doi:10.1016/j.molimm.2005.10.018 · Cited by 14
“…at dA/dT Indeed, pol η physically interacts with Msh2 (Wilson et al., 2005) and displays a preference in inserting transition at dA/dT (Rogozin et al., 2001; Zeng et al., 2001; Delbos et al., 2005; Martomo et al., 2005), consistent with the predominant dA/dT transitions in the VH 1-DXP′ 1-JH5 DNA.”
BackgroundSafra, M., Werner, L., Peres, A., Polak, P., Salamon, N., Schvimer, M., Weiss, B., Barshack, I., Shouval, D. S., & Yaari, G. (2022) · Genome Research · doi:10.1101/gr.276683.122 · Cited by 16
“The other is the WA/TW sites, driven mostly by the low-fidelity DNA Pol η (Zeng et al. 2001; Yavuz et al. 2002).”
Feltes, B. C., & Menck, C. F. M. (2022) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2022.108436 · Cited by 15
Involvement of DNase γ in the resected double-strand DNA breaks in immunoglobulin genes
Okamoto, M., Okamoto, N., Yashiro, H., et al. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.11.142 · Cited by 13
Checkpoint kinase 1 negatively regulates somatic hypermutation
Frankenberger, S., Davari, K., Fischer‐Burkart, S., Böttcher, K., Tomi, N.-S., Zimber‐Strobl, U., & Jungnickel, B. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1378 · Cited by 13
“An alternative uracil-processing mechanism apparently relies on non-canonical mismatch repair, which activates PCNA ubiquitination and recruitment of polymerase Z, leading to mutations at A and T residues (8,9).”
BackgroundSomatic hypermutation does not require Rad54 and Rad54B‐mediated homologous recombination
Bross, L., Wesoły, J., Buerstedde, J., Kanaar, R., & Jacobs, H. (2003) · European Journal of Immunology · doi:10.1002/immu.200310009 · Cited by 13
Campo, V. A., Patenaude, A., Kaden, S., Horb, L. D., Firka, D., Jiricny, J., & Noia, J. M. D. (2013) · Nucleic Acids Research · doi:10.1093/nar/gks1470 · Cited by 12
“The molecular mechanism of MMR-mediated diversification of Ig genes remains to be elucidated, but genetic experiments implicated exonuclease I (18), DNA polymerase Z (19,20) and monoubiquitylated proliferating cell nuclear antigen (21,22) in this process.”
Oertell, K., Florián, J., Haratipour, P., Crans, D. C., Kashemirov, B. A., Wilson, S. H., McKenna, C. E., & Goodman, M. F. (2019) · Biochemistry · doi:10.1021/acs.biochem.9b00087 · Cited by 12
Response 1 to 'Smaller role for pol η?'
Rogozin, I. B., Pavlov, Y. I., & Kunkel, T. A. (2001) · Nature Immunology · doi:10.1038/ni1101-983 · Cited by 12
Inherited Defects of Immunoglobulin Class Switch Recombination
Kracker, S., Gardës, P., & Durandy, A. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-6448-9_15 · Cited by 12
Langerak, P., Krijger, P. H. L., Heideman, M. R., van den Berk, P. C. M., & Jacobs, H. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0223 · Cited by 14
“B (2009) very similar phenotype was observed in B cells from PolhK/K and MMR-deficient MSH2K/K or MSH6K/K mice (Jacobs et al. 1998; Rada et al. 1998; Zeng et al. 2001; Delbos et al. 2005).”
BackgroundIg gene somatic hypermutation in mice defective for DNA polymerase delta proofreading
Longacre, A. (2003) · International Immunology · doi:10.1093/intimm/dxg047 · Cited by 12
“All or some of these appear, nevertheless, to be involved and, in fact, the deficiency in pol h has been shown to lead to an altered mutation spectrum ( 21 ).”
BackgroundReverse Transcriptase Mechanism of Somatic Hypermutation: 60 Years of Clonal Selection Theory
Steele, E. J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01611 · Cited by 11
“DNA Polymerase eta is the A:T mutator in SHM in humans (52)”
BackgroundInfluentialMalvezzi, S., Sturla, S. J., & Tanasova, M. (2015) · Analytical Biochemistry · doi:10.1016/j.ab.2015.03.002 · Cited by 11
On the molecular mechanism of somatic hypermutation of rearranged immunoglobulin genes
Franklin, A., & Blanden, R. V. (2004) · Immunology and Cell Biology · doi:10.1111/j.1440-1711.2004.01289.x · Cited by 11
IJspeert, H., van Schouwenburg, P. A., Pico‐Knijnenburg, I., Loeffen, J. L. C., Brugières, L., Driessen, G. J. A., Blattmann, C., Suerink, M., Januszkiewicz‐Lewandowska, D., Azizi, A. A., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01913 · Cited by 11
A novel cytidine deaminase AIDs in the delivery of error-prone polymerases to immunoglobulin genes
Diaz, M. (2003) · DNA repair · doi:10.1016/s1568-7864(02)00240-9 · Cited by 11
Steele, E. J. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.03.040 · Cited by 11
RNA-directed DNA repair and antibody somatic hypermutation
Franklin, A., & Steele, E. J. (2021) · Trends in Genetics · doi:10.1016/j.tig.2021.10.005 · Cited by 10
Alkyladenine DNA glycosylase (Aag) in somatic hypermutation and class switch recombination
Longerich, S., Meira, L. B., Shah, D., Samson, L. D., & Storb, U. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.06.012 · Cited by 10
“Polη deficiency in mice and humans also leads to a SHM pattern characterized by a low frequency of mutations at A [12-16].”
BackgroundXeroderma Pigmentosum Variant, XP-V: Its Product and Biological Roles
Masutani, C., Hanaoka, F., & Ahmad, S. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-09599-8_10 · Cited by 10
Dörner, T., & Lipsky, P. E. (2001) · Nature Immunology · doi:10.1038/ni1101-982 · Cited by 10
Activation-induced cytidine deaminase acts on double-strand breaks in vitro
SHEN, H. (2006) · Molecular Immunology · doi:10.1016/j.molimm.2006.03.015 · Cited by 9
Metadata
- Authors
- Zeng, X., Winter, D. B., Kasmer, C., Kraemer, K. H., Lehmann, A. R., & Gearhart, P. J.
- Affiliations
- National Institutes of Health (US)
- Walter Reed Army Institute of Research (US)
- University of Sussex (GB)
- Corresponding author
- Gearhart, Patricia J.
- Venue
- Nature Immunology
- Published
- 2001-06
- Volume
- 2
- Issue
- 6
- Pages
- 537-541
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- OpenAlex
- W1560486125
- Semantic Scholar
- 8a9d17ca74ddcb4e43d0ff02f4b768b9cb457829
- Cited by
- 420
- References
- 49
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 6 · 2023: 6 · 2022: 7 · 2021: 11 · 2020: 12 · 2019: 12 · 2018: 10 · 2017: 10 · 2016: 11 · 2015: 8 · 2014: 12 · 2013: 15 · 2012: 15
- FWCI
- 13.73
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Cancer Institute (Z01BC004517)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Keywords
- DNA polymerase eta, somatic hypermutation, immunoglobulin variable region genes, xeroderma pigmentosum variant, peripheral blood lymphocytes, error-prone mutagenesis
- MeSH terms
- Y-Family DNA Polymerases, Animals, B-Lymphocytes, Base Sequence, DNA, DNA-Directed DNA Polymerase, Genes, Immunoglobulin, Humans, Immunoglobulin Variable Region, Molecular Sequence Data, Mutation, Xeroderma Pigmentosum, Base Pairing, Mice
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