• 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

Ime1 和 Ime2 对于酿酒酵母在非发酵碳源上的假菌丝生长是必需的。

Ime1 and Ime2 are required for pseudohyphal growth of Saccharomyces cerevisiae on nonfermentable carbon sources.

机构信息

Durham University, School of Biological and Biomedical Sciences, Durham DH1 3LE, United Kingdom.

出版信息

Mol Cell Biol. 2010 Dec;30(23):5514-30. doi: 10.1128/MCB.00390-10. Epub 2010 Sep 27.

DOI:10.1128/MCB.00390-10
PMID:20876298
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2976428/
Abstract

Pseudohyphal growth and meiosis are two differentiation responses to nitrogen starvation of diploid Saccharomyces cerevisiae. Nitrogen starvation in the presence of fermentable carbon sources is thought to induce pseudohyphal growth, whereas nitrogen and sugar starvation induces meiosis. In contrast to the genetic background routinely used to study pseudohyphal growth (Σ1278b), nonfermentable carbon sources stimulate pseudohyphal growth in the efficiently sporulating strain SK1. Pseudohyphal SK1 cells can exit pseudohyphal growth to complete meiosis. Two stimulators of meiosis, Ime1 and Ime2, are required for pseudohyphal growth of SK1 cells in the presence of nonfermentable carbon sources. Epistasis analysis suggests that Ime1 and Ime2 act in the same order in pseudohyphal growth as in meiosis. The different behaviors of strains SK1 and Σ1278b are in part attributable to differences in cyclic AMP (cAMP) signaling. In contrast to Σ1278b cells, hyperactivation of cAMP signaling using constitutively active Ras2(G19V) inhibited pseudohyphal growth in SK1 cells. Our data identify the SK1 genetic background as an alternative genetic background for the study of pseudohyphal growth and suggest an overlap between signaling pathways controlling pseudohyphal growth and meiosis. Based on these findings, we propose to include exit from pseudohyphal growth and entry into meiosis in the life cycle of S. cerevisiae.

摘要

假菌丝生长和减数分裂是二倍体酿酒酵母氮饥饿时的两种分化反应。在可发酵碳源存在的氮饥饿被认为诱导假菌丝生长,而氮和糖饥饿诱导减数分裂。与通常用于研究假菌丝生长的遗传背景(Σ1278b)不同,不可发酵碳源刺激高效产孢菌株 SK1 的假菌丝生长。假菌丝 SK1 细胞可以退出假菌丝生长以完成减数分裂。两种减数分裂的刺激物 Ime1 和 Ime2,是 SK1 细胞在不可发酵碳源存在下进行假菌丝生长所必需的。上位性分析表明,Ime1 和 Ime2 在假菌丝生长中的作用顺序与减数分裂相同。菌株 SK1 和 Σ1278b 的不同行为部分归因于环腺苷酸 (cAMP) 信号的差异。与 Σ1278b 细胞相反,使用组成性激活 Ras2(G19V) 过度激活 cAMP 信号抑制了 SK1 细胞的假菌丝生长。我们的数据确定了 SK1 遗传背景作为研究假菌丝生长的替代遗传背景,并表明控制假菌丝生长和减数分裂的信号通路之间存在重叠。基于这些发现,我们建议将假菌丝生长的退出和进入减数分裂纳入酿酒酵母的生命周期。

相似文献

1
Ime1 and Ime2 are required for pseudohyphal growth of Saccharomyces cerevisiae on nonfermentable carbon sources.Ime1 和 Ime2 对于酿酒酵母在非发酵碳源上的假菌丝生长是必需的。
Mol Cell Biol. 2010 Dec;30(23):5514-30. doi: 10.1128/MCB.00390-10. Epub 2010 Sep 27.
2
The in vivo activity of Ime1, the key transcriptional activator of meiosis-specific genes in Saccharomyces cerevisiae, is inhibited by the cyclic AMP/protein kinase A signal pathway through the glycogen synthase kinase 3-beta homolog Rim11.Ime1是酿酒酵母中减数分裂特异性基因的关键转录激活因子,其体内活性受到环磷酸腺苷/蛋白激酶A信号通路通过糖原合酶激酶3-β同源物Rim11的抑制。
Mol Cell Biol. 2004 Aug;24(16):6967-79. doi: 10.1128/MCB.24.16.6967-6979.2004.
3
Bipartite structure of an early meiotic upstream activation sequence from Saccharomyces cerevisiae.酿酒酵母早期减数分裂上游激活序列的二分结构。
Mol Cell Biol. 1993 Apr;13(4):2172-81. doi: 10.1128/mcb.13.4.2172-2181.1993.
4
The S. cerevisiae nitrogen starvation-induced Yvh1p and Ptp2p phosphatases play a role in control of sporulation.酿酒酵母氮饥饿诱导的Yvh1p和Ptp2p磷酸酶在孢子形成的控制中发挥作用。
Yeast. 1996 Sep 15;12(11):1135-51. doi: 10.1002/(sici)1097-0061(19960915)12:11<1135::aid-yea11>3.0.co;2-l.
5
Glucose and nitrogen regulate the switch from histone deacetylation to acetylation for expression of early meiosis-specific genes in budding yeast.葡萄糖和氮调节出芽酵母中早期减数分裂特异性基因表达时从组蛋白去乙酰化到乙酰化的转变。
Mol Cell Biol. 2004 Jun;24(12):5197-208. doi: 10.1128/MCB.24.12.5197-5208.2004.
6
IME1 gene encodes a transcription factor which is required to induce meiosis in Saccharomyces cerevisiae.IME1基因编码一种转录因子,该转录因子是酿酒酵母诱导减数分裂所必需的。
Dev Genet. 1994;15(2):139-47. doi: 10.1002/dvg.1020150204.
7
The Ras/cAMP pathway and the CDK-like kinase Ime2 regulate the MAPK Smk1 and spore morphogenesis in Saccharomyces cerevisiae.Ras/cAMP信号通路和类周期蛋白依赖性激酶Ime2调节酿酒酵母中的丝裂原活化蛋白激酶Smk1和孢子形态发生。
Genetics. 2009 Feb;181(2):511-23. doi: 10.1534/genetics.108.098434. Epub 2008 Dec 15.
8
Ime2, a meiosis-specific kinase in yeast, is required for destabilization of its transcriptional activator, Ime1.Ime2是酵母中一种减数分裂特异性激酶,其转录激活因子Ime1的去稳定化需要Ime2。
Mol Cell Biol. 2002 Apr;22(7):2047-56. doi: 10.1128/MCB.22.7.2047-2056.2002.
9
The Ime2 protein kinase family in fungi: more duties than just meiosis.真菌中的 Ime2 蛋白激酶家族:不仅仅在减数分裂中发挥作用。
Mol Microbiol. 2011 Apr;80(1):1-13. doi: 10.1111/j.1365-2958.2011.07575.x. Epub 2011 Mar 1.
10
Stimulation of later functions of the yeast meiotic protein kinase Ime2p by the IDS2 gene product.IDS2基因产物对酵母减数分裂蛋白激酶Ime2p后期功能的刺激作用。
Mol Cell Biol. 1995 Oct;15(10):5279-87. doi: 10.1128/MCB.15.10.5279.

引用本文的文献

1
Protein kinase Ime2 is associated with mycelial growth, conidiation, osmoregulation, and pathogenicity in Fusarium oxysporum.蛋白激酶 Ime2 与腐皮镰刀菌菌丝生长、产孢、渗透压调节和致病性有关。
Arch Microbiol. 2022 Jul 5;204(8):455. doi: 10.1007/s00203-022-02964-0.
2
Distinct requirements for the COMPASS core subunits Set1, Swd1, and Swd3 during meiosis in the budding yeast Saccharomyces cerevisiae.在酿酒酵母有丝分裂过程中,COMPASS 核心亚基 Set1、Swd1 和 Swd3 有不同的需求。
G3 (Bethesda). 2021 Oct 19;11(11). doi: 10.1093/g3journal/jkab283.
3
Investigating the Smuts: Common Cues, Signaling Pathways, and the Role of in Dimorphic Switching and Pathogenesis.探究黑粉菌:常见线索、信号通路以及(此处原文缺失成分)在双态转换和致病过程中的作用
J Fungi (Basel). 2020 Dec 16;6(4):368. doi: 10.3390/jof6040368.
4
Protein Kinase Ime2 Is Required for Mycelial Growth, Conidiation, Osmoregulation, and Pathogenicity in Nematode-Trapping Fungus .蛋白激酶Ime2是捕食线虫真菌菌丝生长、产孢、渗透调节和致病性所必需的。
Front Microbiol. 2020 Jan 14;10:3065. doi: 10.3389/fmicb.2019.03065. eCollection 2019.
5
The Mechanisms of Mating in Pathogenic Fungi-A Plastic Trait.致病真菌的交配机制——一种可塑性特征。
Genes (Basel). 2019 Oct 21;10(10):831. doi: 10.3390/genes10100831.
6
An Evolutionary Perspective on Yeast Mating-Type Switching.酵母交配型转换的进化视角
Genetics. 2017 May;206(1):9-32. doi: 10.1534/genetics.117.202036.
7
Similar environments but diverse fates: Responses of budding yeast to nutrient deprivation.相似的环境却有着不同的命运:出芽酵母对营养剥夺的反应。
Microb Cell. 2016 Aug;3(8):302-328. doi: 10.15698/mic2016.08.516.
8
Rpl22 is required for IME1 mRNA translation and meiotic induction in S. cerevisiae.Rpl22对于酿酒酵母中IME1 mRNA的翻译和减数分裂诱导是必需的。
Cell Div. 2016 Jul 29;11:10. doi: 10.1186/s13008-016-0024-3. eCollection 2016.
9
Fine-tuning of histone H3 Lys4 methylation during pseudohyphal differentiation by the CDK submodule of RNA polymerase II.RNA聚合酶II的CDK亚模块在假菌丝分化过程中对组蛋白H3赖氨酸4甲基化的微调。
Genetics. 2015 Feb;199(2):435-53. doi: 10.1534/genetics.114.172841. Epub 2014 Dec 1.
10
Diversification of a protein kinase cascade: IME-2 is involved in nonself recognition and programmed cell death in Neurospora crassa.蛋白激酶级联的多样化:IME-2 参与了粗糙脉孢菌中非己识别和程序性细胞死亡。
Genetics. 2012 Oct;192(2):467-82. doi: 10.1534/genetics.112.142612. Epub 2012 Jul 18.

本文引用的文献

1
Deregulation of DSE1 gene expression results in aberrant budding within the birth scar and cell wall integrity pathway activation in Saccharomyces cerevisiae.DSE1基因表达失调导致酿酒酵母芽痕内异常出芽以及细胞壁完整性途径激活。
Eukaryot Cell. 2009 Apr;8(4):586-94. doi: 10.1128/EC.00376-08. Epub 2009 Feb 27.
2
A Mep2-dependent transcriptional profile links permease function to gene expression during pseudohyphal growth in Saccharomyces cerevisiae.一种依赖于Mep2的转录图谱将通透酶功能与酿酒酵母假菌丝生长过程中的基因表达联系起来。
Mol Biol Cell. 2008 Jul;19(7):3028-39. doi: 10.1091/mbc.e08-01-0033. Epub 2008 Apr 23.
3
The C-terminal region of the meiosis-specific protein kinase Ime2 mediates protein instability and is required for normal spore formation in budding yeast.减数分裂特异性蛋白激酶Ime2的C末端区域介导蛋白质不稳定性,并且是芽殖酵母中正常孢子形成所必需的。
J Mol Biol. 2008 Apr 18;378(1):31-43. doi: 10.1016/j.jmb.2008.02.001. Epub 2008 Feb 12.
4
UME6, a novel filament-specific regulator of Candida albicans hyphal extension and virulence.UME6,一种新型的白色念珠菌菌丝延伸和毒力的丝状特异性调节因子。
Mol Biol Cell. 2008 Apr;19(4):1354-65. doi: 10.1091/mbc.e07-11-1110. Epub 2008 Jan 23.
5
Meiosis-specific destruction of the Ume6p repressor by the Cdc20-directed APC/C.由Cdc20导向的后期促进复合物对Ume6p阻遏物进行减数分裂特异性破坏。
Mol Cell. 2007 Sep 21;27(6):951-61. doi: 10.1016/j.molcel.2007.08.019.
6
The yeast ammonium transport protein Mep2 and its positive regulator, the Npr1 kinase, play an important role in normal and pseudohyphal growth on various nitrogen media through retrieval of excreted ammonium.酵母铵转运蛋白Mep2及其正向调节因子Npr1激酶,通过回收分泌的铵,在各种氮源培养基上的正常生长和假菌丝生长中发挥重要作用。
Mol Microbiol. 2007 Apr;64(2):534-46. doi: 10.1111/j.1365-2958.2007.05681.x.
7
Faithful modeling of transient expression and its application to elucidating negative feedback regulation.瞬时表达的忠实建模及其在阐明负反馈调节中的应用。
Proc Natl Acad Sci U S A. 2007 Apr 10;104(15):6241-6. doi: 10.1073/pnas.0611168104. Epub 2007 Mar 30.
8
The Use of Linear Asci for Chromosome Mapping in Saccharomyces.线性四分体在酿酒酵母染色体作图中的应用
Genetics. 1955 Jul;40(4):511-8. doi: 10.1093/genetics/40.4.511.
9
Ordered Linear Tetrads Are Produced by the Sporulation of Newly Formed Zygotes of Saccharomyces cerevisiae.有序线性四联体是由酿酒酵母新形成的合子孢子形成产生的。
Genetics. 1987 Feb;115(2):229-32. doi: 10.1093/genetics/115.2.229.
10
Arg-Pro-X-Ser/Thr is a consensus phosphoacceptor sequence for the meiosis-specific Ime2 protein kinase in Saccharomyces cerevisiae.精氨酸-脯氨酸-X-丝氨酸/苏氨酸是酿酒酵母中减数分裂特异性Ime2蛋白激酶的共有磷酸化接受序列。
Biochemistry. 2007 Jan 9;46(1):271-8. doi: 10.1021/bi061858p.