• 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

整合蛋白质组学和转录组学分析揭示了参与集胞藻 PCC 6803 盐胁迫响应的新基因和调控机制。

Integrated proteomic and transcriptomic analysis reveals novel genes and regulatory mechanisms involved in salt stress responses in Synechocystis sp. PCC 6803.

机构信息

School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072, People's Republic of China.

出版信息

Appl Microbiol Biotechnol. 2013 Sep;97(18):8253-64. doi: 10.1007/s00253-013-5139-8. Epub 2013 Aug 8.

DOI:10.1007/s00253-013-5139-8
PMID:23925534
Abstract

Salt stress is a common stress that limits growth and productivity of photosynthetic microbes in natural environments. Although cellular responses of a model cyanobacterium Synechocystis sp. PCC6803 to high and changing salt concentration have been studied, it remains undefined of the gene components and their regulation in the long-term salt acclimation networks. In this study, we performed an integrated study coupling a quantitative iTRAQ-LC-MS/MS proteomics and a next-generation sequencing-based RNA-seq transcriptomics on Synechocystis under salt stress for an extended period of time. Comparative quantification of protein abundances led to the identification of 68 and 108 proteins differentially regulated by salt treatment at 24 and 48 h, respectively. RNA-seq transcriptomic analysis showed that genes involved in energy metabolism and protein synthesis, and genes encoding hypothetical proteins responded to salt stress in a phase-dependent pattern. Notably, a gene encoding CO2-uptake-related protein (CupA) and three genes encoding hypothetical proteins were induced significantly at either transcript or protein level after long-term salt stress. Gene knockout and comparative growth analysis demonstrated that these four genes were involved in salt tolerance in Synechocystis. In addition, a complementary proteome and transcriptome analysis showed that concordance between protein abundances and their corresponding mRNAs varied significantly between various gene-protein pairs, indicating divergent regulation of transcriptional and post-transcriptional processes during salt stress adaptation in Synechocystis. The study provided new insights on genes and regulatory mechanism involved in salt stress response in Synechocystis.

摘要

盐胁迫是限制光合微生物在自然环境中生长和生产力的常见胁迫。尽管已经研究了模式蓝藻集胞藻 PCC6803 对高盐和变化盐浓度的细胞反应,但长期盐适应网络中的基因组成及其调控仍未确定。在这项研究中,我们对盐胁迫下的集胞藻进行了一项整合研究,结合了定量 iTRAQ-LC-MS/MS 蛋白质组学和基于下一代测序的 RNA-seq 转录组学。蛋白质丰度的比较定量导致分别在 24 和 48 小时的盐处理下鉴定出 68 和 108 个差异调节的蛋白质。RNA-seq 转录组分析表明,与能量代谢和蛋白质合成相关的基因以及编码假设蛋白的基因以相位依赖的模式对盐胁迫作出响应。值得注意的是,在长期盐胁迫后,一个编码 CO2 摄取相关蛋白 (CupA) 的基因和三个编码假设蛋白的基因在转录或蛋白质水平上均显著诱导。基因敲除和比较生长分析表明,这四个基因参与集胞藻的耐盐性。此外,互补的蛋白质组和转录组分析表明,蛋白质丰度与其相应 mRNA 之间的一致性在各种基因-蛋白对之间差异很大,表明在集胞藻适应盐胁迫过程中,转录和转录后过程的调控存在分歧。该研究为集胞藻中盐胁迫反应涉及的基因和调控机制提供了新的见解。

相似文献

1
Integrated proteomic and transcriptomic analysis reveals novel genes and regulatory mechanisms involved in salt stress responses in Synechocystis sp. PCC 6803.整合蛋白质组学和转录组学分析揭示了参与集胞藻 PCC 6803 盐胁迫响应的新基因和调控机制。
Appl Microbiol Biotechnol. 2013 Sep;97(18):8253-64. doi: 10.1007/s00253-013-5139-8. Epub 2013 Aug 8.
2
Complementary iTRAQ proteomics and RNA-seq transcriptomics reveal multiple levels of regulation in response to nitrogen starvation in Synechocystis sp. PCC 6803.互补的iTRAQ蛋白质组学和RNA测序转录组学揭示了集胞藻PCC 6803对氮饥饿响应的多层次调控。
Mol Biosyst. 2013 Oct;9(10):2565-74. doi: 10.1039/c3mb70188c.
3
Systematic characterization of hypothetical proteins in Synechocystis sp. PCC 6803 reveals proteins functionally relevant to stress responses.系统分析集胞藻 PCC 6803 中的假定蛋白,揭示了与应激反应功能相关的蛋白。
Gene. 2013 Jan 1;512(1):6-15. doi: 10.1016/j.gene.2012.10.004. Epub 2012 Oct 12.
4
Proteome analysis of salt stress response in the cyanobacterium Synechocystis sp. strain PCC 6803.集胞藻PCC 6803盐胁迫应答的蛋白质组分析
Proteomics. 2006 May;6(9):2733-45. doi: 10.1002/pmic.200500538.
5
Comparative analysis of the hspA mutant and wild-type Synechocystis sp. strain PCC 6803 under salt stress: evaluation of the role of hspA in salt-stress management.盐胁迫下hspA突变型和野生型集胞藻PCC 6803菌株的比较分析:评估hspA在盐胁迫应对中的作用
Arch Microbiol. 2004 Dec;182(6):487-97. doi: 10.1007/s00203-004-0733-x. Epub 2004 Oct 12.
6
Metabolomic analysis of the salt-sensitive mutants reveals changes in amino acid and fatty acid composition important to long-term salt stress in Synechocystis sp. PCC 6803.对盐敏感突变体的代谢组学分析揭示了集胞藻PCC 6803中对长期盐胁迫至关重要的氨基酸和脂肪酸组成的变化。
Funct Integr Genomics. 2014 Jun;14(2):431-40. doi: 10.1007/s10142-014-0370-7. Epub 2014 Mar 19.
7
Proteomic study of the impact of Hik33 mutation in Synechocystis sp. PCC 6803 under normal and salt stress conditions.在正常和盐胁迫条件下突变 Hik33 对集胞藻 6803 影响的蛋白质组学研究。
J Proteome Res. 2012 Jan 1;11(1):502-14. doi: 10.1021/pr200811s. Epub 2011 Nov 16.
8
Identification of the proteomic changes in Synechocystis sp. PCC 6803 following prolonged UV-B irradiation.延长紫外线B照射后集胞藻PCC 6803蛋白质组变化的鉴定
J Exp Bot. 2009;60(4):1141-54. doi: 10.1093/jxb/ern356. Epub 2009 Mar 4.
9
A transcriptional regulator Sll0794 regulates tolerance to biofuel ethanol in photosynthetic Synechocystis sp. PCC 6803.转录调节因子Sll0794调控光合集胞藻PCC 6803对生物燃料乙醇的耐受性。
Mol Cell Proteomics. 2014 Dec;13(12):3519-32. doi: 10.1074/mcp.M113.035675. Epub 2014 Sep 19.
10
An orphan two-component response regulator Slr1588 involves salt tolerance by directly regulating synthesis of compatible solutes in photosynthetic Synechocystis sp. PCC 6803.孤儿双组分响应调节因子Slr1588通过直接调控光合集胞藻PCC 6803中相容性溶质的合成来参与耐盐性。
Mol Biosyst. 2014 Jul;10(7):1765-74. doi: 10.1039/c4mb00095a. Epub 2014 Apr 9.

引用本文的文献

1
Using Publicly Available RNA-seq Data for Expression Analysis of Genes of Interest.利用公共 RNA-seq 数据进行感兴趣基因的表达分析。
Methods Mol Biol. 2024;2792:241-250. doi: 10.1007/978-1-0716-3802-6_19.
2
Photosynthetic efficiency and transcriptome analysis of under hypersaline: a retrograde signaling mechanism in the chloroplast.高盐胁迫下[具体植物名称未给出]的光合效率及转录组分析:叶绿体中的逆行信号传导机制
Front Plant Sci. 2023 Jun 21;14:1192258. doi: 10.3389/fpls.2023.1192258. eCollection 2023.
3
Environment-driven shifts in interindividual variation and phenotypic integration within subnetworks of the mussel transcriptome and proteome.
环境驱动的贻贝转录组和蛋白质组亚网络个体间变异性和表型整合的变化。
Mol Ecol. 2022 Jun;31(11):3112-3127. doi: 10.1111/mec.16452. Epub 2022 Apr 11.
4
Integrative analysis of the salt stress response in cyanobacteria.蓝细菌盐胁迫响应的综合分析。
Biol Direct. 2021 Dec 14;16(1):26. doi: 10.1186/s13062-021-00316-4.
5
CyanoOmicsDB: an integrated omics database for functional genomic analysis of cyanobacteria.氰基组学数据库:一种综合组学数据库,用于蓝藻功能基因组分析。
Nucleic Acids Res. 2022 Jan 7;50(D1):D758-D764. doi: 10.1093/nar/gkab891.
6
Physiological and Proteomic Studies of the Cyanobacterium Anabaena sp. Acclimated to Desiccation Stress.鱼腥藻适应干旱胁迫的生理和蛋白质组学研究。
Curr Microbiol. 2021 Jun;78(6):2429-2439. doi: 10.1007/s00284-021-02504-x. Epub 2021 May 13.
7
Genetic, Genomics, and Responses to Stresses in Cyanobacteria: Biotechnological Implications.蓝藻中的遗传、基因组学和应激反应:生物技术的影响。
Genes (Basel). 2021 Mar 29;12(4):500. doi: 10.3390/genes12040500.
8
Absence of KpsM (Slr0977) Impairs the Secretion of Extracellular Polymeric Substances (EPS) and Impacts Carbon Fluxes in sp. PCC 6803.KpsM(Slr0977)缺失会影响 sp. PCC 6803 细胞外聚合物质(EPS)的分泌并影响碳通量。
mSphere. 2021 Jan 27;6(1):e00003-21. doi: 10.1128/mSphere.00003-21.
9
Recent advances in synthetic biology of cyanobacteria for improved chemicals production.蓝藻合成生物学的最新进展,用于提高化学品的生产。
Bioengineered. 2020 Dec;11(1):1208-1220. doi: 10.1080/21655979.2020.1837458.
10
Responses of Membranes and the Photosynthetic Apparatus to Salt Stress in Cyanobacteria.蓝藻中膜与光合机构对盐胁迫的响应
Front Plant Sci. 2020 Jun 5;11:713. doi: 10.3389/fpls.2020.00713. eCollection 2020.