• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Activation-induced deoxycytidine deaminase: Structural basis for favoring WRC hot motif specificities unique among APOBEC family members.

作者信息

Pham Phuong, Afif Samir A, Shimoda Mayuko, Maeda Kazuhiko, Sakaguchi Nobuo, Pedersen Lars C, Goodman Myron F

机构信息

Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089, United States.

Department of Immunology, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Chuo-ku, Kumamoto 860-8556, Japan; Laboratory of Host Defence, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamada-oka, Suita 565-0871, Japan; World Premier International Research Center Initiative, Immunology Frontier Research Center, Osaka University, 3-1 Yamada-oka, Suita 565-0871, Japan.

出版信息

DNA Repair (Amst). 2017 Jun;54:8-12. doi: 10.1016/j.dnarep.2017.03.007. Epub 2017 Mar 28.

DOI:10.1016/j.dnarep.2017.03.007
PMID:28388461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6408873/
Abstract
摘要

相似文献

1
Activation-induced deoxycytidine deaminase: Structural basis for favoring WRC hot motif specificities unique among APOBEC family members.激活诱导的胞苷脱氨酶:在载脂蛋白B mRNA编辑酶催化多肽样家族成员中独特偏好WRC热点基序特异性的结构基础。
DNA Repair (Amst). 2017 Jun;54:8-12. doi: 10.1016/j.dnarep.2017.03.007. Epub 2017 Mar 28.
2
APOBEC and ADAR deaminases may cause many single nucleotide polymorphisms curated in the OMIM database.载脂蛋白B mRNA编辑酶催化多肽样蛋白(APOBEC)和腺苷脱氨酶(ADAR)可能导致在线孟德尔遗传数据库(OMIM)中整理的许多单核苷酸多态性。
Mutat Res. 2018 Jul;810:33-38. doi: 10.1016/j.mrfmmm.2018.03.008. Epub 2018 Jun 22.
3
Structural basis of substrate specificity in human cytidine deaminase family APOBEC3s.人源胞嘧啶脱氨酶家族 APOBEC3 底物特异性的结构基础。
J Biol Chem. 2021 Aug;297(2):100909. doi: 10.1016/j.jbc.2021.100909. Epub 2021 Jun 24.
4
RNA binding to APOBEC deaminases; Not simply a substrate for C to U editing.APOBEC 脱氨酶的 RNA 结合;不仅仅是 C 到 U 编辑的底物。
RNA Biol. 2017 Sep 2;14(9):1153-1165. doi: 10.1080/15476286.2016.1259783. Epub 2016 Nov 21.
5
Family-Wide Comparative Analysis of Cytidine and Methylcytidine Deamination by Eleven Human APOBEC Proteins.十一种人类载脂蛋白B mRNA编辑酶催化多肽样蛋白(APOBEC)对胞嘧啶和甲基胞嘧啶脱氨基作用的全家族比较分析
J Mol Biol. 2017 Jun 16;429(12):1787-1799. doi: 10.1016/j.jmb.2017.04.021. Epub 2017 May 4.
6
The interesting relationship between APOBEC3 deoxycytidine deaminases and cancer: a long road ahead.APOBEC3 脱氨酶与癌症之间有趣的关系:前路漫漫。
Open Biol. 2020 Dec;10(12):200188. doi: 10.1098/rsob.200188. Epub 2020 Dec 9.
7
The APOBEC Protein Family: United by Structure, Divergent in Function.载脂蛋白B编辑酶催化多肽(APOBEC)蛋白家族:结构统一,功能各异。
Trends Biochem Sci. 2016 Jul;41(7):578-594. doi: 10.1016/j.tibs.2016.05.001. Epub 2016 Jun 6.
8
The preferred nucleotide contexts of the AID/APOBEC cytidine deaminases have differential effects when mutating retrotransposon and virus sequences compared to host genes.与宿主基因相比,AID/APOBEC胞苷脱氨酶的偏好性核苷酸上下文在使逆转座子和病毒序列发生突变时具有不同的作用。
PLoS Comput Biol. 2017 Mar 31;13(3):e1005471. doi: 10.1371/journal.pcbi.1005471. eCollection 2017 Mar.
9
AID Recognizes Structured DNA for Class Switch Recombination.活化诱导胞嘧啶脱氨酶识别用于类别转换重组的结构化DNA。
Mol Cell. 2017 Aug 3;67(3):361-373.e4. doi: 10.1016/j.molcel.2017.06.034. Epub 2017 Jul 27.
10
Structural analysis of the activation-induced deoxycytidine deaminase required in immunoglobulin diversification.免疫球蛋白多样化所需的活化诱导的脱氧胞苷脱氨酶的结构分析
DNA Repair (Amst). 2016 Jul;43:48-56. doi: 10.1016/j.dnarep.2016.05.029. Epub 2016 May 13.

引用本文的文献

1
Regulated somatic hypermutation enhances antibody affinity maturation.受调控的体细胞高频突变增强抗体亲和力成熟。
Nature. 2025 May;641(8062):495-502. doi: 10.1038/s41586-025-08728-2. Epub 2025 Mar 19.
2
Apobec-mediated retroviral hypermutation in vivo is dependent on mouse strain.Apobec 介导的逆转录病毒体内超突变依赖于小鼠品系。
PLoS Pathog. 2024 Aug 29;20(8):e1012505. doi: 10.1371/journal.ppat.1012505. eCollection 2024 Aug.
3
Activation-induced cytidine deaminase an antibody diversification enzyme interacts with chromatin modifier UBN1 in B-cells.激活诱导的胞嘧啶脱氨酶是一种抗体多样化酶,它与 B 细胞中的染色质修饰酶 UBN1 相互作用。
Sci Rep. 2023 Nov 10;13(1):19615. doi: 10.1038/s41598-023-46448-7.
4
APOBEC Reporter Systems for Evaluating diNucleotide Editing Levels.用于评估二核苷酸编辑水平的 APOBEC 报告系统。
CRISPR J. 2023 Oct;6(5):430-446. doi: 10.1089/crispr.2023.0027. Epub 2023 Sep 6.
5
Chickens, more than humans, focus the diversity of their immunoglobulin genes on the complementarity-determining region but utilise amino acids, indicative of a more cross-reactive antibody repertoire.鸡比人类更能将免疫球蛋白基因的多样性集中在互补决定区,但利用的氨基酸则表明其具有更具交叉反应性的抗体库。
Front Immunol. 2022 Dec 8;13:837246. doi: 10.3389/fimmu.2022.837246. eCollection 2022.
6
The role of HIRA-dependent H3.3 deposition and its modifications in the somatic hypermutation of immunoglobulin variable regions.HIRA 依赖性 H3.3 沉积及其修饰在免疫球蛋白可变区体细胞超突变中的作用。
Proc Natl Acad Sci U S A. 2021 Dec 14;118(50). doi: 10.1073/pnas.2114743118.
7
Efficient CRISPR-mediated base editing in spp.在 spp. 中高效的 CRISPR 介导的碱基编辑
Proc Natl Acad Sci U S A. 2021 Jan 12;118(2). doi: 10.1073/pnas.2013338118. Epub 2020 Dec 21.
8
AID assists DNMT1 to attenuate BCL6 expression through DNA methylation in diffuse large B-cell lymphoma cell lines.AID 通过 DNA 甲基化辅助 DNMT1 减弱弥漫性大 B 细胞淋巴瘤细胞系中 BCL6 的表达。
Neoplasia. 2020 Mar;22(3):142-153. doi: 10.1016/j.neo.2020.01.002. Epub 2020 Feb 12.
9
Current insights into the mechanism of mammalian immunoglobulin class switch recombination.哺乳动物免疫球蛋白类别转换重组机制的最新研究进展。
Crit Rev Biochem Mol Biol. 2019 Aug;54(4):333-351. doi: 10.1080/10409238.2019.1659227. Epub 2019 Sep 11.
10
A fluorescent reporter for quantification and enrichment of DNA editing by APOBEC-Cas9 or cleavage by Cas9 in living cells.一种荧光报告基因,用于定量和富集 APOBEC-Cas9 或 Cas9 在活细胞中的 DNA 编辑或切割。
Nucleic Acids Res. 2018 Aug 21;46(14):e84. doi: 10.1093/nar/gky332.

本文引用的文献

1
The novel activation-induced deoxycytidine deaminase (AID) mutants, AIDv and AIDvΔ15 are defective in SHM and CSR.新型激活诱导的胞嘧啶脱氨酶(AID)突变体AIDv和AIDvΔ15在体细胞高频突变(SHM)和类别转换重组(CSR)方面存在缺陷。
DNA Repair (Amst). 2017 May;53:1-3. doi: 10.1016/j.dnarep.2017.02.015. Epub 2017 Mar 6.
2
Structural basis for targeted DNA cytosine deamination and mutagenesis by APOBEC3A and APOBEC3B.载脂蛋白B mRNA编辑酶催化多肽样3A(APOBEC3A)和载脂蛋白B mRNA编辑酶催化多肽样3B(APOBEC3B)靶向DNA胞嘧啶脱氨和诱变的结构基础
Nat Struct Mol Biol. 2017 Feb;24(2):131-139. doi: 10.1038/nsmb.3344. Epub 2016 Dec 19.
3
Structural analysis of the activation-induced deoxycytidine deaminase required in immunoglobulin diversification.免疫球蛋白多样化所需的活化诱导的脱氧胞苷脱氨酶的结构分析
DNA Repair (Amst). 2016 Jul;43:48-56. doi: 10.1016/j.dnarep.2016.05.029. Epub 2016 May 13.
4
Activation-induced deoxycytidine deaminase (AID) co-transcriptional scanning at single-molecule resolution.单分子分辨率下激活诱导的胞嘧啶脱氨酶(AID)的共转录扫描
Nat Commun. 2015 Dec 18;6:10209. doi: 10.1038/ncomms10209.
5
A mathematical model for scanning and catalysis on single-stranded DNA, illustrated with activation-induced deoxycytidine deaminase.用于单链 DNA 扫描和催化的数学模型,以激活诱导的脱氧胞苷脱氨酶为例。
J Biol Chem. 2013 Oct 11;288(41):29786-95. doi: 10.1074/jbc.M113.506550. Epub 2013 Aug 26.
6
A biochemical analysis linking APOBEC3A to disparate HIV-1 restriction and skin cancer.一种将 APOBEC3A 与不同的 HIV-1 限制和皮肤癌联系起来的生化分析。
J Biol Chem. 2013 Oct 11;288(41):29294-304. doi: 10.1074/jbc.M113.504175. Epub 2013 Aug 26.
7
APOBEC3B is an enzymatic source of mutation in breast cancer.APOBEC3B 是乳腺癌突变的酶源。
Nature. 2013 Feb 21;494(7437):366-70. doi: 10.1038/nature11881. Epub 2013 Feb 6.
8
Biochemical analysis of hypermutation by the deoxycytidine deaminase APOBEC3A.APOBEC3A 脱氨酶的超突变的生化分析。
J Biol Chem. 2012 Aug 31;287(36):30812-22. doi: 10.1074/jbc.M112.393181. Epub 2012 Jul 20.
9
A structural basis for the biochemical behavior of activation-induced deoxycytidine deaminase class-switch recombination-defective hyper-IgM-2 mutants.激活诱导的脱氧胞苷脱氨酶类转换重组缺陷性高 IgM-2 突变体的生化行为的结构基础。
J Biol Chem. 2012 Aug 10;287(33):28007-16. doi: 10.1074/jbc.M112.370189. Epub 2012 Jun 19.
10
Analysis of a single-stranded DNA-scanning process in which activation-induced deoxycytidine deaminase (AID) deaminates C to U haphazardly and inefficiently to ensure mutational diversity.分析单链 DNA 扫描过程,在此过程中,激活诱导的脱氨酶(AID)随机且低效地将 C 脱氨为 U,以确保突变多样性。
J Biol Chem. 2011 Jul 15;286(28):24931-42. doi: 10.1074/jbc.M111.241208. Epub 2011 May 12.