• 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

一个涉及 Spa2 SHD 结构域的正反馈环有助于焦点极化。

A positive feedback loop involving the Spa2 SHD domain contributes to focal polarization.

机构信息

Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, United States of America.

Department of Computer Science, University of North Carolina Asheville, Asheville, NC, United States of America.

出版信息

PLoS One. 2022 Feb 8;17(2):e0263347. doi: 10.1371/journal.pone.0263347. eCollection 2022.

DOI:10.1371/journal.pone.0263347
PMID:35134079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8824340/
Abstract

Focal polarization is necessary for finely arranged cell-cell interactions. The yeast mating projection, with its punctate polarisome, is a good model system for this process. We explored the critical role of the polarisome scaffold protein Spa2 during yeast mating with a hypothesis motivated by mathematical modeling and tested by in vivo experiments. Our simulations predicted that two positive feedback loops generate focal polarization, including a novel feedback pathway involving the N-terminal domain of Spa2. We characterized the latter using loss-of-function and gain-of-function mutants. The N-terminal region contains a Spa2 Homology Domain (SHD) which is conserved from yeast to humans, and when mutated largely reproduced the spa2Δ phenotype. Our work together with published data show that the SHD domain recruits Msb3/4 that stimulates Sec4-mediated transport of Bud6 to the polarisome. There, Bud6 activates Bni1-catalyzed actin cable formation, recruiting more Spa2 and completing the positive feedback loop. We demonstrate that disrupting this loop at any point results in morphological defects. Gain-of-function perturbations partially restored focal polarization in a spa2 loss-of-function mutant without restoring localization of upstream components, thus supporting the pathway order. Thus, we have collected data consistent with a novel positive feedback loop that contributes to focal polarization during pheromone-induced polarization in yeast.

摘要

焦点极化对于细胞间精细排列的相互作用是必要的。酵母交配突起,带有点状极化体,是研究这一过程的良好模型系统。我们通过数学建模提出假设,并通过体内实验进行检验,探索了极化体支架蛋白 Spa2 在酵母交配过程中的关键作用。我们的模拟预测,两个正反馈回路会产生焦点极化,包括一个涉及 Spa2 N 端结构域的新反馈途径。我们使用功能丧失和功能获得突变体对后者进行了表征。N 端区域包含一个从酵母到人类都保守的 Spa2 同源结构域 (SHD),当突变时,很大程度上再现了 spa2Δ 表型。我们的工作与已发表的数据一起表明,SHD 结构域招募 Msb3/4,刺激 Sec4 介导的 Bud6 向极化体的运输。在那里,Bud6 激活 Bni1 催化的肌动蛋白电缆形成,募集更多的 Spa2,并完成正反馈回路。我们证明,在任何一点破坏这个循环都会导致形态缺陷。功能获得扰动部分恢复了 spa2 功能丧失突变体中的焦点极化,而没有恢复上游成分的定位,从而支持了途径的顺序。因此,我们收集的数据与一个新的正反馈回路一致,该回路有助于在酵母中诱导极化的交配突起过程中的焦点极化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/dacfad7ce153/pone.0263347.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/f97fbd113704/pone.0263347.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/da781a673f3c/pone.0263347.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/211e23219b17/pone.0263347.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/76540106e8c0/pone.0263347.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/0626f49d5f65/pone.0263347.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/fe0d05fbfae8/pone.0263347.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/738c1740ff13/pone.0263347.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/0c02810d651b/pone.0263347.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/fcafff53625d/pone.0263347.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/dacfad7ce153/pone.0263347.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/f97fbd113704/pone.0263347.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/da781a673f3c/pone.0263347.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/211e23219b17/pone.0263347.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/76540106e8c0/pone.0263347.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/0626f49d5f65/pone.0263347.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/fe0d05fbfae8/pone.0263347.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/738c1740ff13/pone.0263347.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/0c02810d651b/pone.0263347.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/fcafff53625d/pone.0263347.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ca/8824340/dacfad7ce153/pone.0263347.g010.jpg

相似文献

1
A positive feedback loop involving the Spa2 SHD domain contributes to focal polarization.一个涉及 Spa2 SHD 结构域的正反馈环有助于焦点极化。
PLoS One. 2022 Feb 8;17(2):e0263347. doi: 10.1371/journal.pone.0263347. eCollection 2022.
2
Regulation of cell polarity by interactions of Msb3 and Msb4 with Cdc42 and polarisome components.通过Msb3和Msb4与Cdc42及极化体组件的相互作用对细胞极性进行调控。
Mol Cell Biol. 2005 Oct;25(19):8567-80. doi: 10.1128/MCB.25.19.8567-8580.2005.
3
Polarisome scaffolder Spa2-mediated macromolecular condensation of Aip5 for actin polymerization.极性蛋白复合物支架蛋白 Spa2 介导的 Aip5 大分子凝聚促进肌动蛋白聚合。
Nat Commun. 2019 Nov 7;10(1):5078. doi: 10.1038/s41467-019-13125-1.
4
The roles of yeast formins and their regulators Bud6 and Bil2 in the pheromone response.酵母formin 及其调控因子 Bud6 和 Bil2 在交配型信息素反应中的作用。
Mol Biol Cell. 2024 Jun 1;35(6):ar85. doi: 10.1091/mbc.E23-11-0459. Epub 2024 Apr 24.
5
Polarized morphogenesis regulator Spa2 is required for the function of putative stretch-activated Ca2+-permeable channel component Mid1 in Saccharomyces cerevisiae.极化形态发生调节因子Spa2是酿酒酵母中假定的牵张激活的Ca2+通透通道成分Mid1发挥功能所必需的。
Eukaryot Cell. 2005 Aug;4(8):1353-63. doi: 10.1128/EC.4.8.1353-1363.2005.
6
Quantitative proteomics reveals a Gα/MAPK signaling hub that controls pheromone-induced cellular polarization in yeast.定量蛋白质组学揭示了一个 Gα/MAPK 信号枢纽,它控制酵母中信息素诱导的细胞极化。
J Proteomics. 2019 Sep 15;207:103467. doi: 10.1016/j.jprot.2019.103467. Epub 2019 Jul 24.
7
Differential activities and regulation of Saccharomyces cerevisiae formin proteins Bni1 and Bnr1 by Bud6.Bud6对酿酒酵母formin蛋白Bni1和Bnr1的差异活性及调控
J Biol Chem. 2005 Jul 29;280(30):28023-33. doi: 10.1074/jbc.M503094200. Epub 2005 May 27.
8
CDK phosphorylates the polarisome scaffold Spa2 to maintain its localization at the site of cell growth.细胞周期蛋白依赖性激酶(CDK)使极化体支架蛋白Spa2磷酸化,以维持其在细胞生长部位的定位。
Mol Microbiol. 2016 Jul;101(2):250-64. doi: 10.1111/mmi.13386. Epub 2016 Apr 20.
9
Spa2p interacts with cell polarity proteins and signaling components involved in yeast cell morphogenesis.Spa2p与参与酵母细胞形态发生的细胞极性蛋白和信号成分相互作用。
Mol Cell Biol. 1998 Jul;18(7):4053-69. doi: 10.1128/MCB.18.7.4053.
10
The role of GYP-3 in cellular morphogenesis of Neurospora crassa: Analyzing its relationship with the polarisome.GYP-3 在粗糙脉孢菌细胞形态发生中的作用:分析其与极体的关系。
Fungal Genet Biol. 2019 Jul;128:49-59. doi: 10.1016/j.fgb.2019.04.003. Epub 2019 Apr 5.

引用本文的文献

1
The roles of yeast formins and their regulators Bud6 and Bil2 in the pheromone response.酵母formin 及其调控因子 Bud6 和 Bil2 在交配型信息素反应中的作用。
Mol Biol Cell. 2024 Jun 1;35(6):ar85. doi: 10.1091/mbc.E23-11-0459. Epub 2024 Apr 24.

本文引用的文献

1
Type V myosin focuses the polarisome and shapes the tip of yeast cells.V型肌球蛋白使极性体聚集并塑造酵母细胞的尖端。
J Cell Biol. 2021 May 3;220(5). doi: 10.1083/jcb.202006193.
2
Mechanistic insights into actin-driven polarity site movement in yeast.肌动蛋白驱动酵母极性位点运动的机制见解。
Mol Biol Cell. 2020 May 1;31(10):1085-1102. doi: 10.1091/mbc.E20-01-0040. Epub 2020 Mar 18.
3
The cell polarity proteins Boi1 and Boi2 direct an actin nucleation complex to sites of exocytosis in .细胞极性蛋白 Boi1 和 Boi2 将肌动蛋白成核复合物靶向到. 的胞吐部位。
J Cell Sci. 2020 Feb 13;133(3):jcs237982. doi: 10.1242/jcs.237982.
4
Polarisome scaffolder Spa2-mediated macromolecular condensation of Aip5 for actin polymerization.极性蛋白复合物支架蛋白 Spa2 介导的 Aip5 大分子凝聚促进肌动蛋白聚合。
Nat Commun. 2019 Nov 7;10(1):5078. doi: 10.1038/s41467-019-13125-1.
5
Mating yeast cells use an intrinsic polarity site to assemble a pheromone-gradient tracking machine.交配酵母细胞利用内在的极性位点来组装一个信息素梯度跟踪机器。
J Cell Biol. 2019 Nov 4;218(11):3730-3752. doi: 10.1083/jcb.201901155. Epub 2019 Sep 30.
6
Cell fusion in yeast is negatively regulated by components of the cell wall integrity pathway.酵母中的细胞融合受到细胞壁完整性途径成分的负调控。
Mol Biol Cell. 2019 Feb 15;30(4):441-452. doi: 10.1091/mbc.E18-04-0236. Epub 2018 Dec 26.
7
Rab5 GTPases are required for optimal TORC2 function.Rab5 GTPases 对于 TORC2 功能的最佳发挥是必需的。
J Cell Biol. 2019 Mar 4;218(3):961-976. doi: 10.1083/jcb.201807154. Epub 2018 Dec 21.
8
Cortical forces and CDC-42 control clustering of PAR proteins for Caenorhabditis elegans embryonic polarization.皮层力和 CDC-42 控制 PAR 蛋白在秀丽隐杆线虫胚胎极性中的聚类。
Nat Cell Biol. 2017 Aug;19(8):988-995. doi: 10.1038/ncb3577. Epub 2017 Jul 24.
9
Role of Polarized G Protein Signaling in Tracking Pheromone Gradients.极化G蛋白信号传导在追踪信息素梯度中的作用。
Dev Cell. 2015 Nov 23;35(4):471-82. doi: 10.1016/j.devcel.2015.10.024.
10
Tracking individual secretory vesicles during exocytosis reveals an ordered and regulated process.在胞吐作用过程中追踪单个分泌囊泡揭示了一个有序且受调控的过程。
J Cell Biol. 2015 Jul 20;210(2):181-9. doi: 10.1083/jcb.201501118. Epub 2015 Jul 13.