• 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

在芽殖酵母细胞周期中,转录本、蛋白质和代谢物的丰度揭示了脂质代谢的协调控制。

Abundances of transcripts, proteins, and metabolites in the cell cycle of budding yeast reveal coordinate control of lipid metabolism.

机构信息

Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843.

Center for Systems and Synthetic Biology, University of Texas at Austin, Austin, TX 78712.

出版信息

Mol Biol Cell. 2020 May 1;31(10):1069-1084. doi: 10.1091/mbc.E19-12-0708. Epub 2020 Mar 4.

DOI:10.1091/mbc.E19-12-0708
PMID:32129706
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7346729/
Abstract

Establishing the pattern of abundance of molecules of interest during cell division has been a long-standing goal of cell cycle studies. Here, for the first time in any system, we present experiment-matched datasets of the levels of RNAs, proteins, metabolites, and lipids from unarrested, growing, and synchronously dividing yeast cells. Overall, transcript and protein levels were correlated, but specific processes that appeared to change at the RNA level (e.g., ribosome biogenesis) did not do so at the protein level, and vice versa. We also found no significant changes in codon usage or the ribosome content during the cell cycle. We describe an unexpected mitotic peak in the abundance of ergosterol and thiamine biosynthesis enzymes. Although the levels of several metabolites changed in the cell cycle, by far the most significant changes were in the lipid repertoire, with phospholipids and triglycerides peaking strongly late in the cell cycle. Our findings provide an integrated view of the abundance of biomolecules in the eukaryotic cell cycle and point to a coordinate mitotic control of lipid metabolism.

摘要

在细胞分裂过程中建立感兴趣分子的丰度模式一直是细胞周期研究的长期目标。在这里,我们首次在任何系统中展示了未经阻滞、生长和同步分裂酵母细胞的 RNA、蛋白质、代谢物和脂质水平的实验匹配数据集。总的来说,转录本和蛋白质水平是相关的,但在 RNA 水平上似乎发生变化的特定过程(例如核糖体生物发生)在蛋白质水平上没有发生,反之亦然。我们还发现,在细胞周期中,密码子使用或核糖体含量没有显著变化。我们描述了固醇和硫胺素生物合成酶丰度在有丝分裂中的意外峰。尽管细胞周期中几种代谢物的水平发生了变化,但到目前为止,脂质库的变化最为显著,磷脂和三酰甘油在细胞周期后期强烈增加。我们的研究结果提供了真核细胞周期中生物分子丰度的综合视图,并指出了脂质代谢的协调有丝分裂控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/3d970d2b46ed/mbc-31-1069-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/6918ff98c8b2/mbc-31-1069-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/1da25ea704c7/mbc-31-1069-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/08ce35bb9a69/mbc-31-1069-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/68364071d600/mbc-31-1069-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/36f5986d338d/mbc-31-1069-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/3d970d2b46ed/mbc-31-1069-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/6918ff98c8b2/mbc-31-1069-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/1da25ea704c7/mbc-31-1069-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/08ce35bb9a69/mbc-31-1069-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/68364071d600/mbc-31-1069-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/36f5986d338d/mbc-31-1069-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3449/7346729/3d970d2b46ed/mbc-31-1069-g006.jpg

相似文献

1
Abundances of transcripts, proteins, and metabolites in the cell cycle of budding yeast reveal coordinate control of lipid metabolism.在芽殖酵母细胞周期中,转录本、蛋白质和代谢物的丰度揭示了脂质代谢的协调控制。
Mol Biol Cell. 2020 May 1;31(10):1069-1084. doi: 10.1091/mbc.E19-12-0708. Epub 2020 Mar 4.
2
Ribosome synthesis meets the cell cycle.核糖体合成与细胞周期相遇。
Curr Opin Microbiol. 2004 Dec;7(6):631-7. doi: 10.1016/j.mib.2004.10.007.
3
Mapping condition-dependent regulation of lipid metabolism in Saccharomyces cerevisiae.绘制酿酒酵母中脂质代谢条件依赖性调控图谱。
G3 (Bethesda). 2013 Nov 6;3(11):1979-95. doi: 10.1534/g3.113.006601.
4
Single-cell proteomic analysis of S. cerevisiae reveals the architecture of biological noise.酿酒酵母的单细胞蛋白质组学分析揭示了生物噪声的结构。
Nature. 2006 Jun 15;441(7095):840-6. doi: 10.1038/nature04785. Epub 2006 May 14.
5
Lipid particles/droplets of the yeast Saccharomyces cerevisiae revisited: lipidome meets proteome.重新审视酿酒酵母的脂质颗粒/液滴:脂质组与蛋白质组的相遇
Biochim Biophys Acta. 2011 Dec;1811(12):1165-76. doi: 10.1016/j.bbalip.2011.07.015. Epub 2011 Jul 26.
6
Cell size is regulated by phospholipids and not by storage lipids in Saccharomyces cerevisiae.在酿酒酵母中,细胞大小由磷脂调节,而非由储存脂质调节。
Curr Genet. 2018 Oct;64(5):1071-1087. doi: 10.1007/s00294-018-0821-0. Epub 2018 Mar 13.
7
Yeast ribosomes: variety is the spice of life.酵母核糖体:多样是生活的调味品。
Cell. 2007 Nov 2;131(3):450-1. doi: 10.1016/j.cell.2007.10.028.
8
Genetic regulation mediated by thiamin pyrophosphate-binding motif in Saccharomyces cerevisiae.酿酒酵母中硫胺素焦磷酸结合基序介导的基因调控。
Mol Microbiol. 2005 Oct;58(2):467-79. doi: 10.1111/j.1365-2958.2005.04835.x.
9
The protein expression landscape of mitosis and meiosis in diploid budding yeast.二倍体芽殖酵母有丝分裂和减数分裂过程中的蛋白质表达图谱。
J Proteomics. 2017 Mar 6;156:5-19. doi: 10.1016/j.jprot.2016.12.016. Epub 2017 Jan 3.
10
Quantitative proteomic analysis of ribosomal protein L35b mutant of Saccharomyces cerevisiae.酿酒酵母核糖体蛋白L35b突变体的定量蛋白质组学分析。
Biochim Biophys Acta. 2010 Apr;1804(4):676-83. doi: 10.1016/j.bbapap.2009.10.014. Epub 2009 Oct 29.

引用本文的文献

1
Dynamic multi-omics and mechanistic modeling approach uncovers novel mechanisms of kidney fibrosis progression.动态多组学与机制建模方法揭示了肾纤维化进展的新机制。
Mol Syst Biol. 2025 Jun 5. doi: 10.1038/s44320-025-00116-2.
2
Regulation of transcription elongation anticipates alternative gene expression strategies across the cell cycle.转录延伸的调控预示着整个细胞周期中不同的基因表达策略。
PLoS One. 2025 May 7;20(5):e0317650. doi: 10.1371/journal.pone.0317650. eCollection 2025.
3
Temporal oscillation of phospholipids promotes metabolic efficiency.

本文引用的文献

1
The R package Rsubread is easier, faster, cheaper and better for alignment and quantification of RNA sequencing reads.Rsubread 软件包在 RNA 测序reads 的比对和定量方面,具有更简单、更快、更便宜和更好的优势。
Nucleic Acids Res. 2019 May 7;47(8):e47. doi: 10.1093/nar/gkz114.
2
Perturbations of Transcription and Gene Expression-Associated Processes Alter Distribution of Cell Size Values in .转录和基因表达相关过程的扰动会改变. 中细胞大小值的分布。
G3 (Bethesda). 2019 Jan 9;9(1):239-250. doi: 10.1534/g3.118.200854.
3
Identification of Novel Protein Lysine Acetyltransferases in Escherichia coli.
磷脂的时间振荡促进代谢效率。
Nat Chem Biol. 2025 Apr 14. doi: 10.1038/s41589-025-01885-5.
4
AUP1 transcriptionally activated by KDM5B reprograms lipid metabolism to promote the malignant progression of cervical cancer.AUP1 通过 KDM5B 转录激活重编程脂质代谢,促进宫颈癌的恶性进展。
Int J Oncol. 2024 Nov;65(5). doi: 10.3892/ijo.2024.5695. Epub 2024 Sep 27.
5
Patterns of protein synthesis in the budding yeast cell cycle: variable or constant?出芽酵母细胞周期中的蛋白质合成模式:可变还是恒定?
Microb Cell. 2024 Aug 20;11:321-327. doi: 10.15698/mic2024.08.835. eCollection 2024.
6
Eukaryotic cell size regulation and its implications for cellular function and dysfunction.真核细胞大小的调节及其对细胞功能和功能障碍的影响。
Physiol Rev. 2024 Oct 1;104(4):1679-1717. doi: 10.1152/physrev.00046.2023. Epub 2024 Jun 20.
7
Translational control of MPS1 links protein synthesis with the initiation of cell division and spindle pole body duplication in Saccharomyces cerevisiae.在酿酒酵母中,MPS1 的翻译调控将蛋白质合成与细胞分裂的起始和纺锤体极体复制联系起来。
Genetics. 2024 Jul 8;227(3). doi: 10.1093/genetics/iyae069.
8
Proteome-scale movements and compartment connectivity during the eukaryotic cell cycle.真核细胞周期中的蛋白质组规模运动和隔室连接性。
Cell. 2024 Mar 14;187(6):1490-1507.e21. doi: 10.1016/j.cell.2024.02.014. Epub 2024 Mar 6.
9
Targeting APEX2 to the mRNA encoding fatty acid synthase β in yeast identifies interacting proteins that control its abundance in the cell cycle.靶向酵母中编码脂肪酸合酶β的 mRNA 的 APEX2 可鉴定出在细胞周期中控制其丰度的相互作用蛋白。
Mol Biol Cell. 2023 Dec 1;34(13):br20. doi: 10.1091/mbc.E23-05-0166. Epub 2023 Oct 4.
10
α-tubulin regulation by 5' introns in Saccharomyces cerevisiae.α-微管蛋白在酿酒酵母中的 5' 内含子调控。
Genetics. 2023 Dec 6;225(4). doi: 10.1093/genetics/iyad163.
大肠杆菌中新型蛋白质赖氨酸乙酰转移酶的鉴定
mBio. 2018 Oct 23;9(5):e01905-18. doi: 10.1128/mBio.01905-18.
4
Cells alter their tRNA abundance to selectively regulate protein synthesis during stress conditions.细胞改变其 tRNA 丰度以选择性地调节应激条件下的蛋白质合成。
Sci Signal. 2018 Sep 4;11(546):eaat6409. doi: 10.1126/scisignal.aat6409.
5
HTRA1-Dependent Cell Cycle Proteomics.HTRA1 依赖性细胞周期蛋白质组学。
J Proteome Res. 2018 Aug 3;17(8):2679-2694. doi: 10.1021/acs.jproteome.8b00129. Epub 2018 Jul 13.
6
Pervasive Protein Thermal Stability Variation during the Cell Cycle.细胞周期中普遍存在的蛋白质热稳定性变化。
Cell. 2018 May 31;173(6):1495-1507.e18. doi: 10.1016/j.cell.2018.03.053. Epub 2018 Apr 26.
7
Modulation of Protein-Interaction States through the Cell Cycle.通过细胞周期调节蛋白质相互作用状态。
Cell. 2018 May 31;173(6):1481-1494.e13. doi: 10.1016/j.cell.2018.03.065. Epub 2018 Apr 26.
8
A Lipid Transfer Protein Signaling Axis Exerts Dual Control of Cell-Cycle and Membrane Trafficking Systems.脂质转移蛋白信号轴对细胞周期和膜运输系统进行双重控制。
Dev Cell. 2018 Feb 5;44(3):378-391.e5. doi: 10.1016/j.devcel.2017.12.026. Epub 2018 Jan 27.
9
Unification of Protein Abundance Datasets Yields a Quantitative Saccharomyces cerevisiae Proteome.蛋白质丰度数据集的统一产生了一个定量的酿酒酵母蛋白质组。
Cell Syst. 2018 Feb 28;6(2):192-205.e3. doi: 10.1016/j.cels.2017.12.004. Epub 2018 Jan 17.
10
Temporal fluxomics reveals oscillations in TCA cycle flux throughout the mammalian cell cycle.时变通量组学揭示了整个哺乳动物细胞周期中 TCA 循环通量的振荡。
Mol Syst Biol. 2017 Nov 6;13(11):953. doi: 10.15252/msb.20177763.