• 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

MSGP:哺乳动物应激颗粒中蛋白质成分的首个数据库。

MSGP: the first database of the protein components of the mammalian stress granules.

机构信息

Department of Biomedical Sciences and Medicine, University of Algarve, Faro, Portugal.

Centre for Biomedical Research, University of Algarve, Faro, Portugal.

出版信息

Database (Oxford). 2019 Jan 1;2019. doi: 10.1093/database/baz031.

DOI:10.1093/database/baz031
PMID:30820574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6395795/
Abstract

In response to different stress stimuli, cells transiently form stress granules (SGs) in order to protect themselves and re-establish homeostasis. Besides these important cellular functions, SGs are now being implicated in different human diseases, such as neurodegenerative disorders and cancer. SGs are ribonucleoprotein granules, constituted by a variety of different types of proteins, RNAs, factors involved in translation and signaling molecules, being capable of regulating mRNA translation to facilitate stress response. However, until now a complete list of the SG components has not been available. Therefore, we aimer at identifying and linting in an open access database all the proteins described so far as components of SGs. The identification was made through an exhaustive search of studies listed in PubMed and double checked. Moreover, for each identified protein several details were also gathered from public databases, such as the molecular function, the cell types in which they were detected, the type of stress stimuli used to induce SG formation and the reference of the study describing the recruitment of the component to SGs. Expression levels in the context of different neurodegenerative diseases were also obtained and are also described in the database. The Mammalian Stress Granules Proteome is available at https://msgp.pt/, being a new and unique open access online database, the first to list all the protein components of the SGs identified so far. The database constitutes an important and valuable tool for researchers in this research area of growing interest.

摘要

为了应对不同的应激刺激,细胞会短暂地形成应激颗粒(SGs),以保护自身并重新建立平衡。除了这些重要的细胞功能外,SGs 现在还与人类的许多疾病有关,如神经退行性疾病和癌症。SGs 是核糖核蛋白颗粒,由多种不同类型的蛋白质、RNA、参与翻译和信号转导的因子组成,能够调节 mRNA 翻译以促进应激反应。然而,到目前为止,还没有一份完整的 SG 成分清单。因此,我们旨在通过在开放获取数据库中搜索已发表的研究,鉴定并列出迄今为止被描述为 SG 成分的所有蛋白质。通过对 PubMed 中列出的研究进行全面搜索,并进行双重检查,实现了鉴定。此外,对于每个鉴定出的蛋白质,还从公共数据库中收集了一些详细信息,如分子功能、检测到的细胞类型、用于诱导 SG 形成的应激刺激类型以及描述该成分招募到 SGs 的研究的参考信息。还在数据库中描述了在不同神经退行性疾病背景下的表达水平。哺乳动物应激颗粒蛋白组学可在 https://msgp.pt/ 获得,它是一个新的、独特的开放获取在线数据库,是第一个列出迄今为止鉴定出的 SG 所有蛋白成分的数据库。该数据库是该研究领域中日益增长的兴趣的研究人员的重要而有价值的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/dc2b076078ad/baz031f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/491a73cd3844/baz031f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/19d995ed6d20/baz031f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/be54aa6a9afa/baz031f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/ace2e7534280/baz031f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/dc2b076078ad/baz031f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/491a73cd3844/baz031f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/19d995ed6d20/baz031f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/be54aa6a9afa/baz031f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/ace2e7534280/baz031f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/6395795/dc2b076078ad/baz031f5.jpg

相似文献

1
MSGP: the first database of the protein components of the mammalian stress granules.MSGP:哺乳动物应激颗粒中蛋白质成分的首个数据库。
Database (Oxford). 2019 Jan 1;2019. doi: 10.1093/database/baz031.
2
Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules.将细胞质病灶分类为哺乳动物应激颗粒的方法。
J Vis Exp. 2017 May 12(123):55656. doi: 10.3791/55656.
3
Newcastle disease virus induces stable formation of stress granules to facilitate viral replication through manipulating host protein translation.新城疫病毒通过操纵宿主蛋白质翻译诱导应激颗粒的稳定形成,以促进病毒复制。
FASEB J. 2017 Apr;31(4):1337-1353. doi: 10.1096/fj.201600980R. Epub 2016 Dec 23.
4
Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases.应激颗粒、氧化应激与神经退行性疾病之间的关系
Oxid Med Cell Longev. 2017;2017:1809592. doi: 10.1155/2017/1809592. Epub 2017 Jan 18.
5
The HTLV-1 Tax protein inhibits formation of stress granules by interacting with histone deacetylase 6.HTLV-1 Tax 蛋白通过与组蛋白去乙酰化酶 6 相互作用抑制应激颗粒的形成。
Oncogene. 2011 Sep 22;30(38):4050-62. doi: 10.1038/onc.2011.120. Epub 2011 May 2.
6
Stress granules in neurodegeneration--lessons learnt from TAR DNA binding protein of 43 kDa and fused in sarcoma.神经退行性变中的应激颗粒——从 TAR DNA 结合蛋白 43kDa 和肉瘤融合蛋白中学到的教训。
FEBS J. 2013 Sep;280(18):4348-70. doi: 10.1111/febs.12287. Epub 2013 May 9.
7
Changing faces of stress: Impact of heat and arsenite treatment on the composition of stress granules.应激的变化面貌:热和亚砷酸盐处理对应激颗粒组成的影响
Wiley Interdiscip Rev RNA. 2020 Nov;11(6):e1596. doi: 10.1002/wrna.1596. Epub 2020 May 3.
8
Stress granules, RNA-binding proteins and polyglutamine diseases: too much aggregation?应激颗粒、RNA 结合蛋白与多聚谷氨酰胺疾病:聚集过度?
Cell Death Dis. 2021 Jun 8;12(6):592. doi: 10.1038/s41419-021-03873-8.
9
Ebola Virus Does Not Induce Stress Granule Formation during Infection and Sequesters Stress Granule Proteins within Viral Inclusions.埃博拉病毒在感染过程中不诱导应激颗粒形成,并将应激颗粒蛋白隔离在病毒包涵体内。
J Virol. 2016 Jul 27;90(16):7268-7284. doi: 10.1128/JVI.00459-16. Print 2016 Aug 15.
10
Relation Between Stress Granules and Cytoplasmic Protein Aggregates Linked to Neurodegenerative Diseases.应激颗粒与神经退行性疾病相关的细胞质蛋白聚集体之间的关系。
Curr Neurol Neurosci Rep. 2018 Nov 8;18(12):107. doi: 10.1007/s11910-018-0914-7.

引用本文的文献

1
DNA-damage-associated protein co-expression network in cardiomyocytes informs on tolerance to genetic variation and disease.心肌细胞中与DNA损伤相关的蛋白质共表达网络揭示了对基因变异和疾病的耐受性。
iScience. 2025 Apr 18;28(5):112474. doi: 10.1016/j.isci.2025.112474. eCollection 2025 May 16.
2
Stress granules: emerging players in neurodegenerative diseases.应激颗粒:神经退行性疾病中的新角色。
Transl Neurodegener. 2025 May 12;14(1):22. doi: 10.1186/s40035-025-00482-9.
3
irCLIP-RNP and Re-CLIP reveal patterns of dynamic protein assemblies on RNA.

本文引用的文献

1
Context-Dependent and Disease-Specific Diversity in Protein Interactions within Stress Granules.应激颗粒内蛋白相互作用的上下文相关和疾病特异性多样性。
Cell. 2018 Jan 25;172(3):590-604.e13. doi: 10.1016/j.cell.2017.12.032.
2
Polysomes, Stress Granules, and Processing Bodies: A Dynamic Triumvirate Controlling Cytoplasmic mRNA Fate and Function.多聚核糖体、应激颗粒和处理体:控制细胞质 mRNA 命运和功能的动态三联体。
Plant Physiol. 2018 Jan;176(1):254-269. doi: 10.1104/pp.17.01468. Epub 2017 Nov 20.
3
The Stress Granule Transcriptome Reveals Principles of mRNA Accumulation in Stress Granules.
irCLIP-RNP和Re-CLIP揭示了RNA上动态蛋白质组装的模式。
Nature. 2025 May;641(8063):769-778. doi: 10.1038/s41586-025-08787-5. Epub 2025 Mar 26.
4
Human cells contain myriad excised linear intron RNAs with links to gene regulation and potential utility as biomarkers.人类细胞中含有大量被切除的线性内含子 RNA,这些 RNA 与基因调控有关,并有作为生物标志物的潜在用途。
PLoS Genet. 2024 Sep 26;20(9):e1011416. doi: 10.1371/journal.pgen.1011416. eCollection 2024 Sep.
5
DNA damage-associated protein co-expression network in cardiomyocytes informs on tolerance to genetic variation and disease.心肌细胞中与DNA损伤相关的蛋白质共表达网络揭示了对遗传变异和疾病的耐受性。
bioRxiv. 2024 Aug 14:2024.08.14.607863. doi: 10.1101/2024.08.14.607863.
6
Therapy-induced secretion of spliceosomal components mediates pro-survival crosstalk between ovarian cancer cells.治疗诱导的剪接体成分分泌介导卵巢癌细胞间的促生存串扰。
Nat Commun. 2024 Jun 19;15(1):5237. doi: 10.1038/s41467-024-49512-6.
7
The polyglutamine protein ATXN2: from its molecular functions to its involvement in disease.多聚谷氨酰胺蛋白 ATXN2:从其分子功能到其在疾病中的作用。
Cell Death Dis. 2024 Jun 14;15(6):415. doi: 10.1038/s41419-024-06812-5.
8
Searching for LINCS to Stress: Using Text Mining to Automate Reference Chemical Curation.寻找 LINCS 应激反应:利用文本挖掘技术实现参考化学物质的自动编目。
Chem Res Toxicol. 2024 Jun 17;37(6):878-893. doi: 10.1021/acs.chemrestox.3c00335. Epub 2024 May 13.
9
Luteolin Is a Potential Immunomodulating Natural Compound against Pulpal Inflammation.木犀草素是一种潜在的牙髓炎症免疫调节天然化合物。
Biomed Res Int. 2024 Jan 25;2024:8864513. doi: 10.1155/2024/8864513. eCollection 2024.
10
Establishment and Validation of a Four-stress Granule-related Gene Signature in Hepatocellular Carcinoma.肝细胞癌中四味抗纤颗粒相关基因特征的建立与验证
J Clin Transl Hepatol. 2024 Jan 28;12(1):1-14. doi: 10.14218/JCTH.2023.00019. Epub 2023 Jul 25.
应激颗粒转录组揭示了应激颗粒中mRNA积累的原理。
Mol Cell. 2017 Nov 16;68(4):808-820.e5. doi: 10.1016/j.molcel.2017.10.015. Epub 2017 Nov 9.
4
Antisense oligonucleotide therapy for spinocerebellar ataxia type 2.2型脊髓小脑共济失调的反义寡核苷酸疗法
Nature. 2017 Apr 20;544(7650):362-366. doi: 10.1038/nature22044. Epub 2017 Apr 12.
5
Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice.ataxin-2的治疗性减少可延长TDP-43小鼠的寿命并减轻病理变化。
Nature. 2017 Apr 20;544(7650):367-371. doi: 10.1038/nature22038. Epub 2017 Apr 12.
6
Unraveling the Role of Ataxin-2 in Metabolism.解析 Ataxin-2 在代谢中的作用。
Trends Endocrinol Metab. 2017 Apr;28(4):309-318. doi: 10.1016/j.tem.2016.12.006. Epub 2017 Jan 21.
7
ATtRACT-a database of RNA-binding proteins and associated motifs.ATtRACT——一个RNA结合蛋白及相关基序的数据库。
Database (Oxford). 2016 Apr 7;2016. doi: 10.1093/database/baw035. Print 2016.
8
Impairment of stress granule assembly via inhibition of the eIF2alpha phosphorylation sensitizes glioma cells to chemotherapeutic agents.通过抑制真核翻译起始因子2α(eIF2α)磷酸化来损害应激颗粒组装会使胶质瘤细胞对化疗药物敏感。
J Neurooncol. 2016 Apr;127(2):253-60. doi: 10.1007/s11060-015-2043-3. Epub 2016 Jan 5.
9
RNA-binding proteins, neural development and the addictions.RNA结合蛋白、神经发育与成瘾
Genes Brain Behav. 2016 Jan;15(1):169-86. doi: 10.1111/gbb.12273.
10
Sorafenib, a multikinase inhibitor, induces formation of stress granules in hepatocarcinoma cells.索拉非尼是一种多激酶抑制剂,可诱导肝癌细胞中应激颗粒的形成。
Oncotarget. 2015 Dec 22;6(41):43927-43. doi: 10.18632/oncotarget.5980.