• 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

顶复门寄生虫中的ApiAP2转录因子

ApiAP2 Transcription Factors in Apicomplexan Parasites.

作者信息

Jeninga Myriam D, Quinn Jennifer E, Petter Michaela

机构信息

Mikrobiologisches Institut-Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, 91054 Erlangen, Germany.

Department of Medicine, The University of Melbourne, Melbourne, VIC 3010, Australia.

出版信息

Pathogens. 2019 Apr 7;8(2):47. doi: 10.3390/pathogens8020047.

DOI:10.3390/pathogens8020047
PMID:30959972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6631176/
Abstract

Apicomplexan parasites are protozoan organisms that are characterised by complex life cycles and they include medically important species, such as the malaria parasite and the causative agents of toxoplasmosis () and cryptosporidiosis ( spp.). Apicomplexan parasites can infect one or more hosts, in which they differentiate into several morphologically and metabolically distinct life cycle stages. These developmental transitions rely on changes in gene expression. In the last few years, the important roles of different members of the ApiAP2 transcription factor family in regulating life cycle transitions and other aspects of parasite biology have become apparent. Here, we review recent progress in our understanding of the different members of the ApiAP2 transcription factor family in apicomplexan parasites.

摘要

顶复门寄生虫是一类原生动物,其特征是具有复杂的生命周期,包括一些具有医学重要性的物种,如疟原虫以及弓形虫病()和隐孢子虫病(隐孢子虫属物种)的病原体。顶复门寄生虫可以感染一个或多个宿主,并在宿主体内分化为几个形态和代谢上截然不同的生命周期阶段。这些发育转变依赖于基因表达的变化。在过去几年中,ApiAP2转录因子家族的不同成员在调节生命周期转变和寄生虫生物学其他方面的重要作用已变得明显。在此,我们综述了在理解顶复门寄生虫中ApiAP2转录因子家族不同成员方面的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fc/6631176/57d0220f53d9/pathogens-08-00047-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fc/6631176/cc0a9e9e3154/pathogens-08-00047-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fc/6631176/57d0220f53d9/pathogens-08-00047-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fc/6631176/cc0a9e9e3154/pathogens-08-00047-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fc/6631176/57d0220f53d9/pathogens-08-00047-g002.jpg

相似文献

1
ApiAP2 Transcription Factors in Apicomplexan Parasites.顶复门寄生虫中的ApiAP2转录因子
Pathogens. 2019 Apr 7;8(2):47. doi: 10.3390/pathogens8020047.
2
The Apicomplexan AP2 family: integral factors regulating Plasmodium development.顶复门AP2家族:疟原虫发育的重要调控因子
Mol Biochem Parasitol. 2011 Mar;176(1):1-7. doi: 10.1016/j.molbiopara.2010.11.014. Epub 2010 Nov 30.
3
Comparative analysis of stage specific gene regulation of apicomplexan parasites: Plasmodium falciparum and Toxoplasma gondii.疟原虫和弓形虫这两种顶复门寄生虫阶段特异性基因调控的比较分析
Infect Disord Drug Targets. 2010 Aug;10(4):303-11. doi: 10.2174/187152610791591593.
4
Unraveling the complexities of ApiAP2 regulation in Plasmodium falciparum.解析疟原虫中 ApiAP2 调控的复杂性。
Trends Parasitol. 2024 Nov;40(11):987-999. doi: 10.1016/j.pt.2024.09.007. Epub 2024 Oct 16.
5
Systematic CRISPR-Cas9-Mediated Modifications of ApiAP2 Genes Reveal Functional Insights into Parasite Development.系统的 CRISPR-Cas9 介导的 ApiAP2 基因修饰揭示了寄生虫发育的功能见解。
mBio. 2017 Dec 12;8(6):e01986-17. doi: 10.1128/mBio.01986-17.
6
TKL family kinases in human apicomplexan pathogens.人类顶复门病原体中的TKL家族激酶。
Mol Biochem Parasitol. 2024 Sep;259:111628. doi: 10.1016/j.molbiopara.2024.111628. Epub 2024 May 6.
7
Transcending Dimensions in Apicomplexan Research: from Two-Dimensional to Three-Dimensional Cultures.在疟原虫研究中超越维度:从二维到三维培养。
Microbiol Mol Biol Rev. 2022 Jun 15;86(2):e0002522. doi: 10.1128/mmbr.00025-22. Epub 2022 Apr 12.
8
Role of ATG3 in the parasite Toxoplasma gondii: autophagy in an early branching eukaryote.ATG3 在寄生虫弓形虫中的作用:早期分支真核生物中的自噬作用。
Autophagy. 2012 Mar;8(3):435-7. doi: 10.4161/auto.19289. Epub 2012 Feb 24.
9
The Centrocone Houses Cell Cycle Regulatory Factors.中央椎体包含细胞周期调控因子。
mBio. 2017 Aug 22;8(4):e00579-17. doi: 10.1128/mBio.00579-17.
10
Perforin-Like Proteins of Apicomplexan Parasites.顶复门寄生虫的穿孔素样蛋白
Front Cell Infect Microbiol. 2020 Sep 15;10:578883. doi: 10.3389/fcimb.2020.578883. eCollection 2020.

引用本文的文献

1
Two distinct SWI/SNF complexes direct chromatin-linked transcriptional programs in .两种不同的SWI/SNF复合物指导……中的染色质相关转录程序。 (原文中“in”后面缺少具体内容)
bioRxiv. 2025 Jul 16:2025.07.16.665172. doi: 10.1101/2025.07.16.665172.
2
Malaria-induced dysregulation of selected micronutrients (Ca, Mg, Na, K, Zn, Fe, Co) and plasma free amino acids; implications for pathogenesis and host immunity in a Nigerian population.疟疾引起的特定微量营养素(钙、镁、钠、钾、锌、铁、钴)和血浆游离氨基酸的失调;对尼日利亚人群发病机制和宿主免疫的影响。
Parasite Epidemiol Control. 2025 Jun 26;30:e00443. doi: 10.1016/j.parepi.2025.e00443. eCollection 2025 Aug.
3

本文引用的文献

1
Transcriptome and histone epigenome of Plasmodium vivax salivary-gland sporozoites point to tight regulatory control and mechanisms for liver-stage differentiation in relapsing malaria.《间日疟原虫唾液腺子孢子转录组和组蛋白表观基因组揭示了在复发疟疾中紧密的调控控制和肝脏阶段分化的机制》
Int J Parasitol. 2019 Jun;49(7):501-513. doi: 10.1016/j.ijpara.2019.02.007. Epub 2019 May 7.
2
Exploration of the Resistome and Druggable Genome Reveals New Mechanisms of Drug Resistance and Antimalarial Targets.抗药基因组和可药用基因组的探索揭示了抗药性新机制和抗疟靶点。
Microbiol Insights. 2018 Nov 27;11:1178636118808529. doi: 10.1177/1178636118808529. eCollection 2018.
3
Transcriptome analysis reveals a de novo DNA element that may interact with chromatin-associated proteins in Plasmodium berghei during erythrocytic development.
转录组分析揭示了一种新的DNA元件,其可能在伯氏疟原虫红细胞发育过程中与染色质相关蛋白相互作用。
Sci Rep. 2025 May 28;15(1):18621. doi: 10.1038/s41598-025-03586-4.
4
Theileria annulata Hijacks Host Signaling: Integrated Phosphoproteomics and Transcriptomics Unveils ERK1/2 as a Central Regulator of Host Transcription Factors.环形泰勒虫劫持宿主信号传导:整合磷酸化蛋白质组学和转录组学揭示ERK1/2是宿主转录因子的核心调节因子。
Mol Cell Proteomics. 2025 Jun;24(6):100992. doi: 10.1016/j.mcpro.2025.100992. Epub 2025 May 12.
5
Deletion of splicing factor Cdc5 in Toxoplasma disrupts transcriptome integrity, induces abortive bradyzoite formation, and prevents acute infection in mice.弓形虫中剪接因子Cdc5的缺失破坏了转录组完整性,诱导了流产型缓殖子的形成,并阻止了小鼠的急性感染。
Nat Commun. 2025 Apr 22;16(1):3769. doi: 10.1038/s41467-025-58805-3.
6
Role of p24δ in Regulating the Transition from Tachyzoite to Bradyzoite Development.p24δ在调节速殖子向缓殖子发育转变中的作用。
Int J Mol Sci. 2025 Apr 3;26(7):3331. doi: 10.3390/ijms26073331.
7
Molecular mechanisms of surface antigen suppression by ApiAP2 and its implications for vaccine development.ApiAP2抑制表面抗原的分子机制及其对疫苗开发的意义。
Vet Res. 2025 Mar 22;56(1):63. doi: 10.1186/s13567-025-01491-2.
8
transcription factor AP2-06B is mutated at high frequency in Southeast Asia but does not associate with drug resistance.转录因子AP2-06B在东南亚地区高频突变,但与耐药性无关。
Front Cell Infect Microbiol. 2025 Jan 6;14:1521152. doi: 10.3389/fcimb.2024.1521152. eCollection 2024.
9
Numerous rRNA molecules form the apicomplexan mitoribosome via repurposed protein and RNA elements.众多核糖体RNA分子通过重新利用的蛋白质和RNA元件形成顶复门生物的线粒体核糖体。
Nat Commun. 2025 Jan 18;16(1):817. doi: 10.1038/s41467-025-56057-9.
10
Structural characterization of the ACDC domain from ApiAP2 proteins, a potential molecular target against apicomplexan parasites.来自ApiAP2蛋白的ACDC结构域的结构表征,一种针对顶复门寄生虫的潜在分子靶点。
Acta Crystallogr D Struct Biol. 2025 Jan 1;81(Pt 1):38-48. doi: 10.1107/S2059798324012518.
Revisiting the initial steps of sexual development in the malaria parasite Plasmodium falciparum.
重新审视疟原虫恶性疟原虫性发育的初始步骤。
Nat Microbiol. 2019 Jan;4(1):144-154. doi: 10.1038/s41564-018-0291-7. Epub 2018 Nov 26.
4
Drug Resistance in .……中的耐药性
Front Microbiol. 2018 Oct 29;9:2587. doi: 10.3389/fmicb.2018.02587. eCollection 2018.
5
Inducing controlled cell cycle arrest and re-entry during asexual proliferation of Plasmodium falciparum malaria parasites.诱导疟原虫无性增殖过程中的细胞周期有丝分裂阻滞和再进入。
Sci Rep. 2018 Nov 8;8(1):16581. doi: 10.1038/s41598-018-34964-w.
6
A synthetic promoter for multi-stage expression to probe complementary functions of adhesins.用于多阶段表达的合成启动子,以探测黏附素的互补功能。
J Cell Sci. 2018 Oct 22;131(20):jcs210971. doi: 10.1242/jcs.210971.
7
Inducible developmental reprogramming redefines commitment to sexual development in the malaria parasite Plasmodium berghei.诱导性发育重编程重新定义了疟原虫伯氏疟原虫对性发育的承诺。
Nat Microbiol. 2018 Nov;3(11):1206-1213. doi: 10.1038/s41564-018-0223-6. Epub 2018 Sep 3.
8
Characterization of the accessible genome in the human malaria parasite Plasmodium falciparum.人类疟疾寄生虫疟原虫中可及基因组的特征。
Nucleic Acids Res. 2018 Oct 12;46(18):9414-9431. doi: 10.1093/nar/gky643.
9
Genome-wide real-time in vivo transcriptional dynamics during Plasmodium falciparum blood-stage development.疟原虫红内期发育过程中全基因组实时体内转录动态。
Nat Commun. 2018 Jul 9;9(1):2656. doi: 10.1038/s41467-018-04966-3.
10
Morbidity, mortality, and long-term consequences associated with diarrhoea from Cryptosporidium infection in children younger than 5 years: a meta-analyses study.儿童感染隐孢子虫腹泻的发病率、死亡率和长期后果:一项荟萃分析研究。
Lancet Glob Health. 2018 Jul;6(7):e758-e768. doi: 10.1016/S2214-109X(18)30283-3.