• 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

相似文献

1
Co-inhibition of Plasmodium falciparum S-adenosylmethionine decarboxylase/ornithine decarboxylase reveals perturbation-specific compensatory mechanisms by transcriptome, proteome, and metabolome analyses.恶性疟原虫S-腺苷甲硫氨酸脱羧酶/鸟氨酸脱羧酶的共同抑制通过转录组、蛋白质组和代谢组分析揭示了扰动特异性补偿机制。
J Biol Chem. 2009 Feb 13;284(7):4635-46. doi: 10.1074/jbc.M807085200. Epub 2008 Dec 10.
2
In the human malaria parasite Plasmodium falciparum, polyamines are synthesized by a bifunctional ornithine decarboxylase, S-adenosylmethionine decarboxylase.在人类疟原虫恶性疟原虫中,多胺由双功能鸟氨酸脱羧酶——S-腺苷甲硫氨酸脱羧酶合成。
J Biol Chem. 2000 Mar 17;275(11):8097-102. doi: 10.1074/jbc.275.11.8097.
3
Plasmodium falciparum spermidine synthase inhibition results in unique perturbation-specific effects observed on transcript, protein and metabolite levels.恶性疟原虫精脒合酶抑制导致转录本、蛋白质和代谢物水平出现独特的、受扰动影响的变化。
BMC Genomics. 2010 Apr 12;11:235. doi: 10.1186/1471-2164-11-235.
4
Adjustment of polyamine contents in Escherichia coli.大肠杆菌中多胺含量的调节
J Bacteriol. 1988 Jul;170(7):3131-5. doi: 10.1128/jb.170.7.3131-3135.1988.
5
Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis.利用阶段特异性代谢网络分析筛选恶性疟原虫中的潜在靶点
Mol Divers. 2015 Nov;19(4):991-1002. doi: 10.1007/s11030-015-9632-0. Epub 2015 Aug 25.
6
Assessing the polyamine metabolism of Plasmodium falciparum as chemotherapeutic target.评估恶性疟原虫的多胺代谢作为化疗靶点。
Mol Biochem Parasitol. 2008 Jul;160(1):1-7. doi: 10.1016/j.molbiopara.2008.03.008. Epub 2008 Mar 25.
7
The Plasmodium falciparum bifunctional ornithine decarboxylase, S-adenosyl-L-methionine decarboxylase, enables a well balanced polyamine synthesis without domain-domain interaction.恶性疟原虫双功能鸟氨酸脱羧酶(S-腺苷-L-甲硫氨酸脱羧酶)能够实现平衡良好的多胺合成,且无需结构域-结构域相互作用。
J Biol Chem. 2001 Aug 10;276(32):29651-6. doi: 10.1074/jbc.M100578200. Epub 2001 Jun 4.
8
Transcriptional responses of Plasmodium falciparum to alpha-difluoromethylornithine-induced polyamine depletion.恶性疟原虫对α-二氟甲基鸟氨酸诱导的多胺耗竭的转录反应。
Biol Chem. 2008 Feb;389(2):111-25. doi: 10.1515/BC.2008.014.
9
Tumour promoter mediated altered expression and regulation of ornithine decarboxylase and S-adenosylmethionine decarboxylase in H-ras-transformed fibrosarcoma cell lines.肿瘤启动子介导的H-ras转化的纤维肉瘤细胞系中鸟氨酸脱羧酶和S-腺苷甲硫氨酸脱羧酶的表达及调控改变
Biochem Cell Biol. 2001;79(1):69-81.
10
The ornithine decarboxylase domain of the bifunctional ornithine decarboxylase/S-adenosylmethionine decarboxylase of Plasmodium falciparum: recombinant expression and catalytic properties of two different constructs.恶性疟原虫双功能鸟氨酸脱羧酶/ S-腺苷甲硫氨酸脱羧酶的鸟氨酸脱羧酶结构域:两种不同构建体的重组表达及催化特性
Biochem J. 2000 Dec 1;352 Pt 2(Pt 2):287-92.

引用本文的文献

1
Transcriptome and Metabolome Analyses Reveal High-Altitude Adaptation in the Qinghai Toad-Headed Lizard .转录组和代谢组分析揭示青海沙蜥的高海拔适应性
Biology (Basel). 2025 Apr 24;14(5):459. doi: 10.3390/biology14050459.
2
A Candidate Bacterial-Type Amino Acid Decarboxylase Is Essential for Male Gamete Exflagellation and Mosquito Transmission of the Malaria Parasite.候选细菌型氨基酸脱羧酶对疟原虫雄性配子的出芽和蚊子传播是必需的。
Infect Immun. 2023 Jul 18;91(7):e0016723. doi: 10.1128/iai.00167-23. Epub 2023 Jun 1.
3
The human malaria parasite can sense environmental changes and respond by antigenic switching.人类疟疾寄生虫能够感知环境变化,并通过抗原转换做出响应。
Proc Natl Acad Sci U S A. 2023 Apr 25;120(17):e2302152120. doi: 10.1073/pnas.2302152120. Epub 2023 Apr 17.
4
Cripowellins Pause Intraerythrocytic Development at the Ring Stage.疟原虫在环状体期的内液泡发育暂停。
Molecules. 2023 Mar 13;28(6):2600. doi: 10.3390/molecules28062600.
5
An Undefined Interaction between Polyamines and Heat Shock Proteins Leads to Cellular Protection in and Proliferating Cells in Various Organisms.多胺和热休克蛋白之间的未定义相互作用导致各种生物中的细胞和增殖细胞的细胞保护。
Molecules. 2023 Feb 10;28(4):1686. doi: 10.3390/molecules28041686.
6
A non-canonical sensing pathway mediates Plasmodium adaptation to amino acid deficiency.非经典感应途径介导疟原虫适应氨基酸缺乏。
Commun Biol. 2023 Feb 21;6(1):205. doi: 10.1038/s42003-023-04566-y.
7
Current and emerging target identification methods for novel antimalarials.新型抗疟药物的现有和新兴靶标鉴定方法。
Int J Parasitol Drugs Drug Resist. 2022 Dec;20:135-144. doi: 10.1016/j.ijpddr.2022.11.001. Epub 2022 Nov 11.
8
S-Adenosylmethionine Synthetase Is Essential for Parasite Survival through a Complex Interaction Network with Cytoplasmic and Nuclear Proteins.S-腺苷甲硫氨酸合成酶通过与细胞质和核蛋白的复杂相互作用网络对寄生虫的存活至关重要。
Microorganisms. 2022 Jul 14;10(7):1419. doi: 10.3390/microorganisms10071419.
9
Machine Learning Uses Chemo-Transcriptomic Profiles to Stratify Antimalarial Compounds With Similar Mode of Action.机器学习利用化转录组特征对作用模式相似的抗疟化合物进行分层。
Front Cell Infect Microbiol. 2021 Jun 29;11:688256. doi: 10.3389/fcimb.2021.688256. eCollection 2021.
10
6'-β-Fluoro-Homoaristeromycin and 6'-Fluoro-Homoneplanocin A Are Potent Inhibitors of Chikungunya Virus Replication through Their Direct Effect on Viral Nonstructural Protein 1.6'-β-氟霍巴他汀和 6'-氟霍巴他霉素是通过直接作用于病毒非结构蛋白 1 而对基孔肯雅病毒复制具有强大抑制作用的药物。
Antimicrob Agents Chemother. 2020 Mar 24;64(4). doi: 10.1128/AAC.02532-19.

本文引用的文献

1
Metabolite profiling of the intraerythrocytic malaria parasite Plasmodium falciparum by (1)H NMR spectroscopy.采用¹H核磁共振波谱法对恶性疟原虫红细胞内期进行代谢物谱分析。
NMR Biomed. 2009 Apr;22(3):292-302. doi: 10.1002/nbm.1323.
2
Dynamic RNA profiling in Plasmodium falciparum synchronized blood stages exposed to lethal doses of artesunate.在暴露于致死剂量青蒿琥酯的恶性疟原虫同步化血液阶段中的动态RNA分析。
BMC Genomics. 2008 Aug 18;9:388. doi: 10.1186/1471-2164-9-388.
3
Specific DNA-binding by apicomplexan AP2 transcription factors.顶复门AP2转录因子的特异性DNA结合
Proc Natl Acad Sci U S A. 2008 Jun 17;105(24):8393-8. doi: 10.1073/pnas.0801993105. Epub 2008 Jun 9.
4
Histone acetyltransferase inhibitor anacardic acid causes changes in global gene expression during in vitro Plasmodium falciparum development.组蛋白乙酰转移酶抑制剂漆树酸在体外恶性疟原虫发育过程中引起全基因组基因表达变化。
Eukaryot Cell. 2008 Jul;7(7):1200-10. doi: 10.1128/EC.00063-08. Epub 2008 May 16.
5
Assessing the polyamine metabolism of Plasmodium falciparum as chemotherapeutic target.评估恶性疟原虫的多胺代谢作为化疗靶点。
Mol Biochem Parasitol. 2008 Jul;160(1):1-7. doi: 10.1016/j.molbiopara.2008.03.008. Epub 2008 Mar 25.
6
Transcriptional responses of Plasmodium falciparum to alpha-difluoromethylornithine-induced polyamine depletion.恶性疟原虫对α-二氟甲基鸟氨酸诱导的多胺耗竭的转录反应。
Biol Chem. 2008 Feb;389(2):111-25. doi: 10.1515/BC.2008.014.
7
Exploring functional genomics for drug target and therapeutics discovery in Plasmodia.探索疟原虫中药物靶点和治疗方法发现的功能基因组学。
Acta Trop. 2008 Feb;105(2):113-23. doi: 10.1016/j.actatropica.2007.10.013. Epub 2007 Nov 12.
8
Mechanisms of gene regulation in Plasmodium.疟原虫中的基因调控机制。
Am J Trop Med Hyg. 2007 Aug;77(2):201-8.
9
Whole-genome analysis of mRNA decay in Plasmodium falciparum reveals a global lengthening of mRNA half-life during the intra-erythrocytic development cycle.恶性疟原虫mRNA降解的全基因组分析揭示了红细胞内发育周期中mRNA半衰期的整体延长。
Genome Biol. 2007;8(7):R134. doi: 10.1186/gb-2007-8-7-r134.
10
Plasmodium falciparum: genome wide perturbations in transcript profiles among mixed stage cultures after chloroquine treatment.恶性疟原虫:氯喹治疗后混合阶段培养物中转录谱的全基因组扰动。
Exp Parasitol. 2007 Sep;117(1):87-92. doi: 10.1016/j.exppara.2007.03.001. Epub 2007 Mar 14.

恶性疟原虫S-腺苷甲硫氨酸脱羧酶/鸟氨酸脱羧酶的共同抑制通过转录组、蛋白质组和代谢组分析揭示了扰动特异性补偿机制。

Co-inhibition of Plasmodium falciparum S-adenosylmethionine decarboxylase/ornithine decarboxylase reveals perturbation-specific compensatory mechanisms by transcriptome, proteome, and metabolome analyses.

作者信息

van Brummelen Anna C, Olszewski Kellen L, Wilinski Daniel, Llinás Manuel, Louw Abraham I, Birkholtz Lyn-Marie

机构信息

Department of Biochemistry, University of Pretoria, Pretoria, Gauteng 0002, South Africa.

出版信息

J Biol Chem. 2009 Feb 13;284(7):4635-46. doi: 10.1074/jbc.M807085200. Epub 2008 Dec 10.

DOI:10.1074/jbc.M807085200
PMID:19073607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3783055/
Abstract

Polyamines are ubiquitous components of all living cells, and their depletion usually causes cytostasis, a strategy employed for treatment of West African trypanosomiasis. To evaluate polyamine depletion as an anti-malarial strategy, cytostasis caused by the co-inhibition of S-adenosylmethionine decarboxylase/ornithine decarboxylase in Plasmodium falciparum was studied with a comprehensive transcriptome, proteome, and metabolome investigation. Highly synchronized cultures were sampled just before and during cytostasis, and a novel zero time point definition was used to enable interpretation of results in lieu of the developmentally regulated control of gene expression in P. falciparum. Transcriptome analysis revealed the occurrence of a generalized transcriptional arrest just prior to the growth arrest due to polyamine depletion. However, the abundance of 538 transcripts was differentially affected and included three perturbation-specific compensatory transcriptional responses as follows: the increased abundance of the transcripts for lysine decarboxylase and ornithine aminotransferase and the decreased abundance of that for S-adenosylmethionine synthetase. Moreover, the latter two compensatory mechanisms were confirmed on both protein and metabolite levels confirming their biological relevance. In contrast with previous reports, the results provide evidence that P. falciparum responds to alleviate the detrimental effects of polyamine depletion via regulation of its transcriptome and subsequently the proteome and metabolome.

摘要

多胺是所有活细胞中普遍存在的成分,其消耗通常会导致细胞停滞,这是一种用于治疗西非锥虫病的策略。为了评估多胺消耗作为一种抗疟疾策略,通过全面的转录组、蛋白质组和代谢组研究,对恶性疟原虫中S-腺苷甲硫氨酸脱羧酶/鸟氨酸脱羧酶的共同抑制所引起的细胞停滞进行了研究。在细胞停滞之前和期间对高度同步化的培养物进行采样,并使用一种新的零时间点定义来解释结果,以代替恶性疟原虫中基因表达的发育调控控制。转录组分析显示,由于多胺消耗导致生长停滞之前出现了普遍的转录停滞。然而,538个转录本的丰度受到不同影响,包括三种特定于扰动的补偿性转录反应,如下所示:赖氨酸脱羧酶和鸟氨酸转氨酶转录本的丰度增加,而S-腺苷甲硫氨酸合成酶转录本的丰度降低。此外,后两种补偿机制在蛋白质和代谢物水平上均得到证实,确认了它们的生物学相关性。与先前的报道相反,这些结果提供了证据,表明恶性疟原虫通过调节其转录组以及随后的蛋白质组和代谢组来应对,以减轻多胺消耗的有害影响。