• 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

APOBEC 蛋白在病毒限制和其他细胞功能中的结构和多聚体状态的研究进展。

Insights into the Structures and Multimeric Status of APOBEC Proteins Involved in Viral Restriction and Other Cellular Functions.

机构信息

Molecular and Computational Biology, Departments of Biological Sciences, Chemistry, University of Southern California, Los Angeles, CA 90089, USA.

Genetic, Molecular and Cellular Biology Program, Keck School of Medicine, Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA 90089, USA.

出版信息

Viruses. 2021 Mar 17;13(3):497. doi: 10.3390/v13030497.

DOI:10.3390/v13030497
PMID:33802945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8002816/
Abstract

lipoprotein mRNA diting atalytic polypeptide-like (APOBEC) proteins belong to a family of deaminase proteins that can catalyze the deamination of cytosine to uracil on single-stranded DNA or/and RNA. APOBEC proteins are involved in diverse biological functions, including adaptive and innate immunity, which are critical for restricting viral infection and endogenous retroelements. Dysregulation of their functions can cause undesired genomic mutations and RNA modification, leading to various associated diseases, such as hyper-IgM syndrome and cancer. This review focuses on the structural and biochemical data on the multimerization status of individual APOBECs and the associated functional implications. Many APOBECs form various multimeric complexes, and multimerization is an important way to regulate functions for some of these proteins at several levels, such as deaminase activity, protein stability, subcellular localization, protein storage and activation, virion packaging, and antiviral activity. The multimerization of some APOBECs is more complicated than others, due to the associated complex RNA binding modes.

摘要

载脂蛋白 B mRNA 编辑酶催化多肽样蛋白(APOBEC)属于脱氨酶蛋白家族,可催化单链 DNA 或/和 RNA 上胞嘧啶脱氨变成尿嘧啶。APOBEC 蛋白参与多种生物学功能,包括适应性和先天性免疫,对限制病毒感染和内源性逆转录元件至关重要。其功能失调会导致非预期的基因组突变和 RNA 修饰,从而导致各种相关疾病,如高免疫球蛋白 M 综合征和癌症。本综述重点介绍了单个 APOBEC 蛋白的多聚化状态及其相关功能意义的结构和生化数据。许多 APOBEC 蛋白形成各种多聚体复合物,多聚化是调节这些蛋白在多个水平上功能的重要方式,如脱氨酶活性、蛋白质稳定性、亚细胞定位、蛋白质储存和激活、病毒包装和抗病毒活性。由于相关的复杂 RNA 结合模式,一些 APOBEC 蛋白的多聚化比其他蛋白更复杂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/1e93038e683a/viruses-13-00497-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/657c830a5874/viruses-13-00497-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/a69e328eeb6c/viruses-13-00497-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/81e9b1308342/viruses-13-00497-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/f03366ba7f77/viruses-13-00497-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/37c2487cb6af/viruses-13-00497-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/930680d852c2/viruses-13-00497-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/1e93038e683a/viruses-13-00497-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/657c830a5874/viruses-13-00497-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/a69e328eeb6c/viruses-13-00497-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/81e9b1308342/viruses-13-00497-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/f03366ba7f77/viruses-13-00497-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/37c2487cb6af/viruses-13-00497-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/930680d852c2/viruses-13-00497-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/8002816/1e93038e683a/viruses-13-00497-g007.jpg

相似文献

1
Insights into the Structures and Multimeric Status of APOBEC Proteins Involved in Viral Restriction and Other Cellular Functions.APOBEC 蛋白在病毒限制和其他细胞功能中的结构和多聚体状态的研究进展。
Viruses. 2021 Mar 17;13(3):497. doi: 10.3390/v13030497.
2
DNA Editing by APOBECs: A Genomic Preserver and Transformer.APOBEC 介导的 DNA 编辑:基因组的保护者和转化者。
Trends Genet. 2016 Jan;32(1):16-28. doi: 10.1016/j.tig.2015.10.005. Epub 2015 Nov 20.
3
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.
4
APOBECs orchestrate genomic and epigenomic editing across health and disease.APOBECs 在健康和疾病中调控基因组和表观基因组编辑。
Trends Genet. 2021 Nov;37(11):1028-1043. doi: 10.1016/j.tig.2021.07.003. Epub 2021 Aug 2.
5
Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands.模拟诱变体的结合:APOBEC 对核酸配体的选择。
Trends Biochem Sci. 2018 Aug;43(8):606-622. doi: 10.1016/j.tibs.2018.04.013. Epub 2018 May 23.
6
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.
7
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.
8
APOBEC-mediated genomic alterations link immunity and viral infection during human papillomavirus-driven cervical carcinogenesis.APOBEC 介导的基因组改变在人乳头瘤病毒驱动的宫颈癌发生过程中连接免疫和病毒感染。
Biosci Trends. 2017 Sep 12;11(4):383-388. doi: 10.5582/bst.2017.01103. Epub 2017 Jul 17.
9
Apolipoprotein B mRNA Editing Enzyme, Catalytic Polypeptide-Like Gene Expression, RNA Editing, and MicroRNAs Regulation.载脂蛋白B信使核糖核酸编辑酶、催化多肽样基因表达、RNA编辑和微小核糖核酸调控
Methods Mol Biol. 2018;1699:75-81. doi: 10.1007/978-1-4939-7435-1_5.
10
Research on the influence of APOBEC family on the occurrence, diagnosis, and treatment of various tumors.载脂蛋白B mRNA编辑酶催化多肽样蛋白(APOBEC)家族对各种肿瘤发生、诊断及治疗的影响研究
J Cancer Res Clin Oncol. 2023 Jan;149(1):357-366. doi: 10.1007/s00432-022-04395-2. Epub 2022 Oct 12.

引用本文的文献

1
APOBEC3-Related Editing and Non-Editing Determinants of HIV-1 and HTLV-1 Restriction.与载脂蛋白B mRNA编辑酶催化多肽样蛋白3相关的HIV-1和HTLV-1限制的编辑及非编辑决定因素
Int J Mol Sci. 2025 Feb 12;26(4):1561. doi: 10.3390/ijms26041561.
2
APOBEC-1 cofactors regulate APOBEC3-induced mutations in hepatitis B virus.载脂蛋白B mRNA编辑酶催化多肽1辅助因子调控乙型肝炎病毒中载脂蛋白B mRNA编辑酶催化多肽3诱导的突变。
J Virol. 2025 Feb 25;99(2):e0187924. doi: 10.1128/jvi.01879-24. Epub 2025 Jan 27.
3
The Role of the Large T Antigen in the Molecular Pathogenesis of Merkel Cell Carcinoma.

本文引用的文献

1
The Role of APOBECs in Viral Replication.载脂蛋白B编辑酶催化多肽样蛋白(APOBECs)在病毒复制中的作用。
Microorganisms. 2020 Nov 30;8(12):1899. doi: 10.3390/microorganisms8121899.
2
Crystal Structure of a Soluble APOBEC3G Variant Suggests ssDNA to Bind in a Channel that Extends between the Two Domains.APOBEC3G 可溶性变体的晶体结构表明 ssDNA 结合在两个结构域之间延伸的通道中。
J Mol Biol. 2020 Nov 20;432(23):6042-6060. doi: 10.1016/j.jmb.2020.10.020. Epub 2020 Oct 22.
3
The structure of APOBEC1 and insights into its RNA and DNA substrate selectivity.
大 T 抗原在 Merkel 细胞癌分子发病机制中的作用。
Genes (Basel). 2024 Aug 27;15(9):1127. doi: 10.3390/genes15091127.
4
Engineered deaminases as a key component of DNA and RNA editing tools.工程脱氨酶作为DNA和RNA编辑工具的关键组成部分。
Mol Ther Nucleic Acids. 2023 Oct 20;34:102062. doi: 10.1016/j.omtn.2023.102062. eCollection 2023 Dec 12.
5
Comprehensive Analysis and Drug Modulation of Human Endogenous Retrovirus in Hepatocellular Carcinomas.肝细胞癌中人类内源性逆转录病毒的综合分析与药物调控
Cancers (Basel). 2023 Jul 18;15(14):3664. doi: 10.3390/cancers15143664.
6
Small-Angle X-ray Scattering (SAXS) Measurements of APOBEC3G Provide Structural Basis for Binding of Single-Stranded DNA and Processivity.小角度 X 射线散射(SAXS)测量法对 APOBEC3G 的研究为单链 DNA 结合和连续性提供了结构基础。
Viruses. 2022 Sep 6;14(9):1974. doi: 10.3390/v14091974.
7
The roles of APOBEC-mediated RNA editing in SARS-CoV-2 mutations, replication and fitness.APOBEC 介导的 RNA 编辑在 SARS-CoV-2 突变、复制和适应性中的作用。
Sci Rep. 2022 Sep 13;12(1):14972. doi: 10.1038/s41598-022-19067-x.
8
The Roles of APOBEC-mediated RNA Editing in SARS-CoV-2 Mutations, Replication and Fitness.载脂蛋白B编辑复合体介导的RNA编辑在严重急性呼吸综合征冠状病毒2突变、复制及适应性中的作用
Res Sq. 2022 Apr 12:rs.3.rs-1524060. doi: 10.21203/rs.3.rs-1524060/v1.
9
The Roles of APOBEC-mediated RNA Editing in SARS-CoV-2 Mutations, Replication and Fitness.载脂蛋白B介导的RNA编辑在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)突变、复制及适应性中的作用
bioRxiv. 2022 Apr 7:2021.12.18.473309. doi: 10.1101/2021.12.18.473309.
10
Special Issue "APOBECs and Virus Restriction".特刊:APOBEC 与病毒限制
Viruses. 2021 Aug 15;13(8):1613. doi: 10.3390/v13081613.
载脂蛋白B编辑酶催化多肽1(APOBEC1)的结构及其对RNA和DNA底物选择性的见解。
NAR Cancer. 2020 Dec;2(4):zcaa027. doi: 10.1093/narcan/zcaa027. Epub 2020 Oct 9.
4
Loop 1 of APOBEC3C Regulates its Antiviral Activity against HIV-1.APOBEC3C 的环 1 调节其对 HIV-1 的抗病毒活性。
J Mol Biol. 2020 Nov 20;432(23):6200-6227. doi: 10.1016/j.jmb.2020.10.014. Epub 2020 Oct 15.
5
Single-nucleotide polymorphism of the DNA cytosine deaminase APOBEC3H haplotype I leads to enzyme destabilization and correlates with lung cancer.DNA胞嘧啶脱氨酶APOBEC3H单倍型I的单核苷酸多态性导致酶不稳定,并与肺癌相关。
NAR Cancer. 2020 Sep;2(3):zcaa023. doi: 10.1093/narcan/zcaa023. Epub 2020 Sep 17.
6
Quantification of ongoing APOBEC3A activity in tumor cells by monitoring RNA editing at hotspots.通过监测热点处的 RNA 编辑来定量肿瘤细胞中的持续 APOBEC3A 活性。
Nat Commun. 2020 Jun 12;11(1):2971. doi: 10.1038/s41467-020-16802-8.
7
AID in Antibody Diversification: There and Back Again.辅助抗体多样化:有去有回。
Trends Immunol. 2020 Jul;41(7):586-600. doi: 10.1016/j.it.2020.04.009. Epub 2020 Apr 27.
8
APOBEC3C Tandem Domain Proteins Create Super Restriction Factors against HIV-1.APOBEC3C 串联结构域蛋白可形成针对 HIV-1 的超级限制因子。
mBio. 2020 Apr 28;11(2):e00737-20. doi: 10.1128/mBio.00737-20.
9
Understanding the structural basis of HIV-1 restriction by the full length double-domain APOBEC3G.理解全长双结构域 APOBEC3G 对 HIV-1 的限制的结构基础。
Nat Commun. 2020 Jan 31;11(1):632. doi: 10.1038/s41467-020-14377-y.
10
Regulation of Antiviral Innate Immunity Through APOBEC Ribonucleoprotein Complexes.通过载脂蛋白B编辑酶催化多肽(APOBEC)核糖核蛋白复合物对抗病毒天然免疫的调控
Subcell Biochem. 2019;93:193-219. doi: 10.1007/978-3-030-28151-9_6.