• 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

蛋白质组学分析揭示了 MoPer1 调控 的发育和致病性的分子机制。

Proteomics Analysis Reveals the Molecular Mechanism of MoPer1 Regulating the Development and Pathogenicity of .

机构信息

State Key Laboratory of Hybrid Rice and Institute of Plant Protection, Hunan Academy of Agricultural Sciences, Changsha, China.

Long Ping Branch, Graduate School of Hunan University, Changsha, China.

出版信息

Front Cell Infect Microbiol. 2022 Jun 24;12:926771. doi: 10.3389/fcimb.2022.926771. eCollection 2022.

DOI:10.3389/fcimb.2022.926771
PMID:35811686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9269092/
Abstract

Glycosylphosphatidylinositol (GPI) anchoring the protein GPI modification post-transcriptionally is commonly seen. In our previous study, MoPer1, a GPI anchoring essential factor, has a critical effect on growth, pathogenicity, and conidiogenesis, but its molecular mechanism is not clear. Here, we extracted the glycoproteins from the Δ mutant and wild-type Guy11 to analyze their differential levels by quantitative proteomic analysis of TMT markers. After background subtraction, a total of 431 proteins, with significant changes in expression, were successfully identified, and these differential proteins were involved in biological regulation, as well as cellular process and metabolic process, binding, catalytic activity, and other aspects. Moreover, we found that MoPer1 regulates the expression of 14 proteins involved in growth, development, and pathogenicity of . The above findings shed light on MoPer1's underlying mechanism in regulating growth, development, and pathogenicity of .

摘要

糖基磷脂酰肌醇(GPI)锚定蛋白的 GPI 修饰是常见的转录后修饰。在我们之前的研究中,GPI 锚定必需因子 MoPer1 对 生长、致病性和分生孢子形成有重要影响,但它的分子机制尚不清楚。在这里,我们从Δ突变体和野生型 Guy11 中提取糖蛋白,通过 TMT 标记的定量蛋白质组学分析来分析它们的差异水平。扣除背景后,成功鉴定出 431 个表达有显著变化的蛋白质,这些差异蛋白参与了生物调节、细胞过程和代谢过程、结合、催化活性等方面。此外,我们发现 MoPer1 调节 14 个与生长、发育和致病性相关蛋白的表达。上述发现为 MoPer1 调节 生长、发育和致病性的潜在机制提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/7585214a4d69/fcimb-12-926771-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/9725522e7b10/fcimb-12-926771-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/6a46fc06fb7a/fcimb-12-926771-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/dfcf17c352ad/fcimb-12-926771-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/a08d2252235c/fcimb-12-926771-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/3a699bd58c53/fcimb-12-926771-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/7585214a4d69/fcimb-12-926771-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/9725522e7b10/fcimb-12-926771-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/6a46fc06fb7a/fcimb-12-926771-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/dfcf17c352ad/fcimb-12-926771-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/a08d2252235c/fcimb-12-926771-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/3a699bd58c53/fcimb-12-926771-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f54/9269092/7585214a4d69/fcimb-12-926771-g006.jpg

相似文献

1
Proteomics Analysis Reveals the Molecular Mechanism of MoPer1 Regulating the Development and Pathogenicity of .蛋白质组学分析揭示了 MoPer1 调控 的发育和致病性的分子机制。
Front Cell Infect Microbiol. 2022 Jun 24;12:926771. doi: 10.3389/fcimb.2022.926771. eCollection 2022.
2
MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae.稻瘟病菌的生长、分生孢子形成及致病性需要MoPer1。
Rice (N Y). 2018 Dec 22;11(1):64. doi: 10.1186/s12284-018-0255-9.
3
The LAMMER Kinase MoKns1 Regulates Growth, Conidiation and Pathogenicity in .LAMMER 激酶 MoKns1 调控. 的生长、产孢和致病性。
Int J Mol Sci. 2022 Jul 22;23(15):8104. doi: 10.3390/ijms23158104.
4
Pleiotropic roles of O-mannosyltransferase MoPmt4 in development and pathogenicity of Magnaporthe oryzae.甘露糖基转移酶 MoPmt4 在稻瘟病菌发育和致病性中的多效作用。
Curr Genet. 2019 Feb;65(1):223-239. doi: 10.1007/s00294-018-0864-2. Epub 2018 Jun 26.
5
Synergistic deletion of RGS1 and COS1 may reduce the pathogenicity of Magnaporthe oryzae.协同缺失 RGS1 和 COS1 可能降低稻瘟病菌的致病性。
Arch Microbiol. 2019 Aug;201(6):807-816. doi: 10.1007/s00203-019-01646-8. Epub 2019 Mar 14.
6
The putative Gγ subunit gene MGG1 is required for conidiation, appressorium formation, mating and pathogenicity in Magnaporthe oryzae.假定的Gγ亚基基因MGG1是稻瘟病菌分生孢子形成、附着胞形成、交配和致病性所必需的。
Curr Genet. 2015 Nov;61(4):641-51. doi: 10.1007/s00294-015-0490-1. Epub 2015 May 6.
7
A Histone Deacetylase, Magnaporthe oryzae RPD3, Regulates Reproduction and Pathogenic Development in the Rice Blast Fungus.一个组蛋白去乙酰化酶,稻瘟病菌 RPD3,调控水稻稻瘟病菌的繁殖和致病性发育。
mBio. 2021 Dec 21;12(6):e0260021. doi: 10.1128/mBio.02600-21. Epub 2021 Nov 16.
8
Is Essential for Morphogenesis and Pathogenicity of Magnaporthe oryzae.对于稻瘟病菌的形态发生和致病性来说是必需的。
mSphere. 2019 Sep 4;4(5):e00309-19. doi: 10.1128/mSphere.00309-19.
9
A putative PKA phosphorylation site S227 in MoSom1 is essential for infection-related morphogenesis and pathogenicity in Magnaporthe oryzae.假定的 MoSom1 中的 PKA 磷酸化位点 S227 对于稻瘟病菌中的感染相关形态发生和致病性是必需的。
Cell Microbiol. 2021 Oct;23(10):e13370. doi: 10.1111/cmi.13370. Epub 2021 Jul 16.
10
MoYcp4 is required for growth, conidiogenesis and pathogenicity in Magnaporthe oryzae.稻瘟病菌的生长、分生孢子形成及致病性需要MoYcp4。
Mol Plant Pathol. 2017 Sep;18(7):1001-1011. doi: 10.1111/mpp.12455. Epub 2016 Aug 28.

引用本文的文献

1
Proteomic lung analysis revealed hyper-activation of neutrophil extracellular trap formation in cases of fatal COVID-19.蛋白质组学肺部分析显示,在致命的新冠病毒疾病(COVID-19)病例中,中性粒细胞胞外诱捕网形成过度激活。
Heliyon. 2024 May 24;10(11):e31878. doi: 10.1016/j.heliyon.2024.e31878. eCollection 2024 Jun 15.

本文引用的文献

1
A self-balancing circuit centered on MoOsm1 kinase governs adaptive responses to host-derived ROS in .一个以 MoOsm1 激酶为中心的自衡电路,调控对宿主来源 ROS 的适应性反应。
Elife. 2020 Dec 4;9:e61605. doi: 10.7554/eLife.61605.
2
Microenvironmental Interplay Predominated by Beneficial Abates Fungal Pathogen Incidence in Paddy Environment.微环境相互作用占主导地位可减少稻田环境中真菌病原体的发生。
Environ Sci Technol. 2019 Nov 19;53(22):13042-13052. doi: 10.1021/acs.est.9b04616. Epub 2019 Nov 4.
3
MoPer1 is required for growth, conidiogenesis, and pathogenicity in Magnaporthe oryzae.
稻瘟病菌的生长、分生孢子形成及致病性需要MoPer1。
Rice (N Y). 2018 Dec 22;11(1):64. doi: 10.1186/s12284-018-0255-9.
4
A Guide to Mass Spectrometry-Based Quantitative Proteomics.基于质谱的定量蛋白质组学指南。
Methods Mol Biol. 2019;1916:3-39. doi: 10.1007/978-1-4939-8994-2_1.
5
Determination of Protein Molecular Weights on SDS-PAGE.十二烷基硫酸钠聚丙烯酰胺凝胶电泳法测定蛋白质分子量
Methods Mol Biol. 2019;1855:101-105. doi: 10.1007/978-1-4939-8793-1_10.
6
eIF4G-an integrator of mRNA metabolism?真核生物翻译起始因子4G——mRNA代谢的整合因子?
FEMS Yeast Res. 2016 Nov;16(7). doi: 10.1093/femsyr/fow087. Epub 2016 Sep 29.
7
MoARG1, MoARG5,6 and MoARG7 involved in arginine biosynthesis are essential for growth, conidiogenesis, sexual reproduction, and pathogenicity in Magnaporthe oryzae.参与精氨酸生物合成的稻瘟病菌MoARG1、MoARG5,6和MoARG7对于稻瘟病菌的生长、分生孢子形成、有性生殖及致病性至关重要。
Microbiol Res. 2015 Nov;180:11-22. doi: 10.1016/j.micres.2015.07.002. Epub 2015 Jul 20.
8
eIF3 targets cell-proliferation messenger RNAs for translational activation or repression.真核起始因子3(eIF3)靶向细胞增殖信使核糖核酸以进行翻译激活或抑制。
Nature. 2015 Jun 4;522(7554):111-4. doi: 10.1038/nature14267. Epub 2015 Apr 6.
9
An S-(hydroxymethyl)glutathione dehydrogenase is involved in conidiation and full virulence in the rice blast fungus Magnaporthe oryzae.一种S-(羟甲基)谷胱甘肽脱氢酶参与稻瘟病菌的分生孢子形成和完全致病性。
PLoS One. 2015 Mar 20;10(3):e0120627. doi: 10.1371/journal.pone.0120627. eCollection 2015.
10
Ribosomal proteins: functions beyond the ribosome.核糖体蛋白:核糖体之外的功能。
J Mol Cell Biol. 2015 Apr;7(2):92-104. doi: 10.1093/jmcb/mjv014. Epub 2015 Mar 3.