Evaluation of APOBEC3B Recognition Motifs by NMR Reveals Preferred Substrates

被引:10
作者
Liu, Manjuan [1 ]
Mallinger, Aurelie [1 ]
Tortorici, Marcello [1 ]
Newbatt, Yvette [1 ]
Richards, Meirion [1 ]
Mirza, Amin [1 ]
van Montfort, Rob L. M. [1 ]
Burke, Rosemary [1 ]
Blagg, Julian [1 ]
Kaserer, Teresa [1 ]
机构
[1] Inst Canc Res, Canc Res UK Canc Therapeut Unit, London SM2 5NG, England
关键词
DNA CYTOSINE; CATALYTIC DOMAIN; STRUCTURAL BASIS; HUMAN CANCERS; DEAMINATION; MUTAGENESIS; RESTRICTION; MUTATION; BINDING;
D O I
10.1021/acschembio.8b00639
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
APOBEC3B (A3B) deamination activity on ssDNA is considered a contributing factor to tumor heterogeneity and drug resistance in a number of human cancers. Despite its clinical impact, little is known about A3B ssDNA substrate preference. We have used nuclear magnetic resonance to monitor the catalytic turnover of A3B substrates in real-time. This study reports preferred nucleotide sequences for A3B substrates, including optimized 4-mer oligonucleotides, and reveals a breadth of substrate recognition that includes DNA sequences known to be mutated in drug-resistant cancer clones. Our results are consistent with available clinical and structural data and may inform the design of substrate-based A3B inhibitors.
引用
收藏
页码:2427 / 2432
页数:6
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[31]   APOBEC3B: Pathological consequences of an innate immune DNA mutator [J].
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[36]   Expression of APOBEC3B mRNA in Primary Breast Cancer of Japanese Women [J].
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Oki, Eiji ;
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[37]   DNA replication stress: a source of APOBEC3B expression in breast cancer [J].
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[38]   Protein kinase A inhibits tumor mutator APOBEC3B through phosphorylation [J].
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Maruyama, Wataru ;
Nagata, Kayoko ;
Tanabe, Fumiko ;
Kobayashi, Masayuki ;
Shindo, Keisuke ;
Morishita, Ryo ;
Sato, Hironori ;
Takaori-Kondo, Akifumi .
SCIENTIFIC REPORTS, 2019, 9 (1)
[39]   Rationally Designed APOBEC3B Cytosine Base Editors with Improved Specificity [J].
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Zhang, Feng ;
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[40]   APOBEC3B up-regulation independently predicts ovarian cancer prognosis: a cohort study [J].
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Zhao, Hongbo .
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