• 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

一个扩展的无 DNA 核内隔室组织疟原虫中的中心体微管。

An extended DNA-free intranuclear compartment organizes centrosome microtubules in malaria parasites.

机构信息

Centre for Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.

Electron Microscopy Core Facility, Heidelberg University, Heidelberg, Germany.

出版信息

Life Sci Alliance. 2021 Sep 17;4(11). doi: 10.26508/lsa.202101199. Print 2021 Nov.

DOI:10.26508/lsa.202101199
PMID:34535568
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8473725/
Abstract

Proliferation of in red blood cells is the cause of malaria and is underpinned by an unconventional cell division mode, called schizogony. Contrary to model organisms, replicates by multiple rounds of nuclear divisions that are not interrupted by cytokinesis. Organization and dynamics of critical nuclear division factors remain poorly understood. Centriolar plaques, the centrosomes of , serve as microtubule organizing centers and have an acentriolar, amorphous structure. The small size of parasite nuclei has precluded detailed analysis of intranuclear microtubule organization by classical fluorescence microscopy. We apply recently developed super-resolution and time-lapse imaging protocols to describe microtubule reconfiguration during schizogony. Analysis of centrin, nuclear pore, and microtubule positioning reveals two distinct compartments of the centriolar plaque. Whereas centrin is extranuclear, we confirm by correlative light and electron tomography that microtubules are nucleated in a previously unknown and extended intranuclear compartment, which is devoid of chromatin but protein-dense. This study generates a working model for an unconventional centrosome and enables a better understanding about the diversity of eukaryotic cell division.

摘要

疟原虫在红细胞中的增殖是疟疾的病因,它依赖于一种非常规的细胞分裂模式,称为裂殖生殖。与模式生物不同,疟原虫通过多次核分裂而不是胞质分裂进行复制。关键核分裂因子的组织和动态仍知之甚少。中心粒斑, 的中心体,充当微管组织中心,具有无中心体的、无定形的结构。寄生虫核的小尺寸使得通过经典荧光显微镜对核内微管组织进行详细分析变得困难。我们应用最近开发的超分辨率和延时成像方案来描述裂殖生殖过程中的微管重排。对中心体蛋白、核孔和微管定位的分析揭示了中心粒斑的两个不同区域。虽然中心体蛋白位于核外,但我们通过共聚焦和电子断层扫描关联确认,微管是在一个以前未知的、扩展的核内区域中被引发的,该区域不含染色质,但富含蛋白质。这项研究为一种非常规的中心体生成了一个工作模型,并使我们更好地理解了真核细胞分裂的多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/00a4f49dbde2/LSA-2021-01199_FigS8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/836cd3fc70d8/LSA-2021-01199_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/fad8823b7044/LSA-2021-01199_FigS1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/37b36dd621b1/LSA-2021-01199_FigS2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/b1e10fd64107/LSA-2021-01199_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/ec21278c3605/LSA-2021-01199_FigS3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/d4404f10070b/LSA-2021-01199_FigS4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/ecd254a51a63/LSA-2021-01199_FigS5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/d505e583ca61/LSA-2021-01199_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/b466e48337fe/LSA-2021-01199_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/cd630774c491/LSA-2021-01199_FigS6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/8c736b1234fb/LSA-2021-01199_FigS7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/00a4f49dbde2/LSA-2021-01199_FigS8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/836cd3fc70d8/LSA-2021-01199_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/fad8823b7044/LSA-2021-01199_FigS1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/37b36dd621b1/LSA-2021-01199_FigS2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/b1e10fd64107/LSA-2021-01199_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/ec21278c3605/LSA-2021-01199_FigS3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/d4404f10070b/LSA-2021-01199_FigS4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/ecd254a51a63/LSA-2021-01199_FigS5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/d505e583ca61/LSA-2021-01199_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/b466e48337fe/LSA-2021-01199_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/cd630774c491/LSA-2021-01199_FigS6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/8c736b1234fb/LSA-2021-01199_FigS7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4368/8473725/00a4f49dbde2/LSA-2021-01199_FigS8.jpg

相似文献

1
An extended DNA-free intranuclear compartment organizes centrosome microtubules in malaria parasites.一个扩展的无 DNA 核内隔室组织疟原虫中的中心体微管。
Life Sci Alliance. 2021 Sep 17;4(11). doi: 10.26508/lsa.202101199. Print 2021 Nov.
2
An Sfi1-like centrin-interacting centriolar plaque protein affects nuclear microtubule homeostasis.一种类似 Sfi1 的中心体蛋白与中心粒相关蛋白相互作用,影响核微管的动态平衡。
PLoS Pathog. 2023 May 2;19(5):e1011325. doi: 10.1371/journal.ppat.1011325. eCollection 2023 May.
3
Depletion of the mini-chromosome maintenance complex binding protein allows the progression of cytokinesis despite abnormal karyokinesis during the asexual development of Plasmodium falciparum.尽管疟原虫无性发育过程中核分异常,但通过耗尽微染色体维持复合物结合蛋白,允许胞质分裂的进行。
Cell Microbiol. 2021 Mar;23(3):e13284. doi: 10.1111/cmi.13284. Epub 2020 Nov 18.
4
Tissue-specific degradation of essential centrosome components reveals distinct microtubule populations at microtubule organizing centers.组织特异性降解必需的中心体成分揭示了微管组织中心处不同的微管种群。
PLoS Biol. 2018 Aug 6;16(8):e2005189. doi: 10.1371/journal.pbio.2005189. eCollection 2018 Aug.
5
Regulated expression of the centrosomal protein DdCP224 affects microtubule dynamics and reveals mechanisms for the control of supernumerary centrosome number.中心体蛋白DdCP224的调控表达影响微管动力学,并揭示了控制多余中心体数量的机制。
Mol Biol Cell. 2003 Oct;14(10):4067-74. doi: 10.1091/mbc.e03-04-0242. Epub 2003 Jun 13.
6
Disruption of microtubules uncouples budding and nuclear division in Toxoplasma gondii.微管的破坏使刚地弓形虫的出芽与核分裂解偶联。
J Cell Sci. 2002 Mar 1;115(Pt 5):1017-25. doi: 10.1242/jcs.115.5.1017.
7
CRK4 links early mitotic events to the onset of S-phase during schizogony.CRK4 将早期有丝分裂事件与裂殖生殖期间 S 期的开始联系起来。
mBio. 2023 Aug 31;14(4):e0077923. doi: 10.1128/mbio.00779-23. Epub 2023 Jun 22.
8
Centrins, cell cycle regulation proteins in human malaria parasite Plasmodium falciparum.中心蛋白,人类疟原虫恶性疟原虫中的细胞周期调节蛋白。
J Biol Chem. 2008 Nov 14;283(46):31871-83. doi: 10.1074/jbc.M800028200. Epub 2008 Aug 8.
9
Remodeling of centrosomes in intraspecies and interspecies nuclear transfer porcine embryos.种内和种间核移植猪胚胎中心体的重塑
Cell Cycle. 2007 Jun 15;6(12):1510-20. Epub 2007 Apr 16.
10
Separate To Operate: the Centriole-Free Inner Core of the Centrosome Regulates the Assembly of the Intranuclear Spindle in .单独操作:中心体无中心粒的内核心调节核内纺锤体的组装。
mBio. 2022 Oct 26;13(5):e0185922. doi: 10.1128/mbio.01859-22. Epub 2022 Sep 7.

引用本文的文献

1
A dynamic barrier: remodeling of the nuclear envelope during closed mitosis in malaria parasites.动态屏障:疟原虫封闭有丝分裂期间核膜的重塑
mSphere. 2025 Jul 29;10(7):e0099924. doi: 10.1128/msphere.00999-24. Epub 2025 Jun 9.
2
mSphere of Influence: The ever-expanding universe of parasite cell biology.影响范围:寄生虫细胞生物学不断扩展的领域。
mSphere. 2025 Mar 25;10(3):e0004325. doi: 10.1128/msphere.00043-25. Epub 2025 Mar 4.
3
DNA replication dynamics are associated with genome composition in Plasmodium species.疟原虫物种中的DNA复制动态与基因组组成相关。

本文引用的文献

1
Asynchronous nuclear cycles in multinucleated facilitate rapid proliferation.多核细胞中的异步核循环有助于快速增殖。
Sci Adv. 2022 Apr;8(13):eabj5362. doi: 10.1126/sciadv.abj5362. Epub 2022 Mar 30.
2
How Many Is Enough? - Challenges of Multinucleated Cell Division in Malaria Parasites.有多少是足够的?——疟原虫多核细胞分裂的挑战。
Front Cell Infect Microbiol. 2021 May 7;11:658616. doi: 10.3389/fcimb.2021.658616. eCollection 2021.
3
Apicomplexans: A conoid ring unites them all.顶复门生物:一个圆锥形环将它们全部连接在一起。
Nucleic Acids Res. 2025 Feb 8;53(4). doi: 10.1093/nar/gkaf111.
4
PfFBXO1 is essential for inner membrane complex formation in Plasmodium falciparum during both asexual and transmission stages.PfFBXO1对于恶性疟原虫在无性繁殖和传播阶段内膜复合体的形成至关重要。
Commun Biol. 2025 Feb 7;8(1):190. doi: 10.1038/s42003-025-07619-6.
5
Nuclear pore complexes undergo Nup221 exchange during blood-stage asexual replication of parasites.在疟原虫血液阶段无性繁殖过程中,核孔复合体经历Nup221交换。
mSphere. 2024 Dec 19;9(12):e0075024. doi: 10.1128/msphere.00750-24. Epub 2024 Nov 11.
6
Detailing organelle division and segregation in Plasmodium falciparum.详述疟原虫细胞器的分裂和隔离。
J Cell Biol. 2024 Dec 2;223(12). doi: 10.1083/jcb.202406064. Epub 2024 Nov 1.
7
Plasmodium NEK1 coordinates MTOC organisation and kinetochore attachment during rapid mitosis in male gamete formation.疟原虫 NEK1 在雄性配子形成的快速有丝分裂过程中协调着微管组织中心的组织和动粒附着。
PLoS Biol. 2024 Sep 10;22(9):e3002802. doi: 10.1371/journal.pbio.3002802. eCollection 2024 Sep.
8
The three Aurora-related kinases display distinct temporal and spatial associations with mitotic structures in asexual blood stage parasites and gametocytes.三种与极光相关的激酶在无性血期寄生虫和配子体中与有丝分裂结构表现出不同的时空关联。
mSphere. 2024 Sep 25;9(9):e0046524. doi: 10.1128/msphere.00465-24. Epub 2024 Sep 5.
9
Enzymatically enhanced ultrastructure expansion microscopy unlocks expansion of cysts.酶增强超微结构膨胀显微镜可实现囊肿的膨胀。
mSphere. 2024 Sep 25;9(9):e0032224. doi: 10.1128/msphere.00322-24. Epub 2024 Aug 27.
10
Disruption of Plasmodium falciparum kinetochore proteins destabilises the nexus between the centrosome equivalent and the mitotic apparatus.疟原虫动基体蛋白的破坏会使中心体等价物和有丝分裂装置之间的连接不稳定。
Nat Commun. 2024 Jul 10;15(1):5794. doi: 10.1038/s41467-024-50167-6.
PLoS Biol. 2021 Mar 11;19(3):e3001105. doi: 10.1371/journal.pbio.3001105. eCollection 2021 Mar.
4
Expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid.扩展显微镜为了解疟疾寄生虫的细胞骨架提供了新的视角,包括锥状体的保守性。
PLoS Biol. 2021 Mar 11;19(3):e3001020. doi: 10.1371/journal.pbio.3001020. eCollection 2021 Mar.
5
The Dynamic Roles of the Inner Membrane Complex in the Multiple Stages of the Malaria Parasite.内膜复合物在疟原虫多个阶段的动态作用
Front Cell Infect Microbiol. 2021 Jan 8;10:611801. doi: 10.3389/fcimb.2020.611801. eCollection 2020.
6
Ultrastructure expansion microscopy (U-ExM).超微结构扩展显微镜(U-ExM)。
Methods Cell Biol. 2021;161:57-81. doi: 10.1016/bs.mcb.2020.05.006. Epub 2020 Jul 1.
7
Kinesin-5 Associates With the Spindle Apparatus During Cell Division and Is Important for Efficient Production of Infectious Sporozoites.在细胞分裂过程中,驱动蛋白-5 与纺锤体装置结合,对于有效产生感染性的子孢子很重要。
Front Cell Infect Microbiol. 2020 Oct 14;10:583812. doi: 10.3389/fcimb.2020.583812. eCollection 2020.
8
The structure of the γ-TuRC: a 25-years-old molecular puzzle.γ-TuRC 的结构:一个 25 岁的分子谜题。
Curr Opin Struct Biol. 2021 Feb;66:15-21. doi: 10.1016/j.sbi.2020.08.008. Epub 2020 Sep 29.
9
Fussing About Fission: Defining Variety Among Mainstream and Exotic Apicomplexan Cell Division Modes.纠结于裂变:定义主流和外来顶复门细胞分裂模式的多样性。
Front Cell Infect Microbiol. 2020 Jun 5;10:269. doi: 10.3389/fcimb.2020.00269. eCollection 2020.
10
Real-time dynamics of NDC80 reveals unusual modes of chromosome segregation during parasite proliferation.NDC80 的实时动态揭示了寄生虫增殖过程中染色体分离的异常模式。
J Cell Sci. 2020 Jun 30;134(5):jcs245753. doi: 10.1242/jcs.245753.