Suppr超能文献

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.

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.
Mol Cell Biol. 2010 Dec;30(23):5514-30. doi: 10.1128/MCB.00390-10. Epub 2010 Sep 27.
3
Bipartite structure of an early meiotic upstream activation sequence from Saccharomyces cerevisiae.
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.
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.
7
The Ras/cAMP pathway and the CDK-like kinase Ime2 regulate the MAPK Smk1 and spore morphogenesis in Saccharomyces cerevisiae.
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.
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.
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.
Mol Cell Biol. 1995 Oct;15(10):5279-87. doi: 10.1128/MCB.15.10.5279.

引用本文的文献

4
Protein Kinase Ime2 Is Required for Mycelial Growth, Conidiation, Osmoregulation, and Pathogenicity in Nematode-Trapping Fungus .
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.
Genes (Basel). 2019 Oct 21;10(10):831. doi: 10.3390/genes10100831.
6
An Evolutionary Perspective on Yeast Mating-Type Switching.
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.
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.
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.
Genetics. 2015 Feb;199(2):435-53. doi: 10.1534/genetics.114.172841. Epub 2014 Dec 1.

本文引用的文献

4
UME6, a novel filament-specific regulator of Candida albicans hyphal extension and virulence.
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.
Mol Cell. 2007 Sep 21;27(6):951-61. doi: 10.1016/j.molcel.2007.08.019.
7
Faithful modeling of transient expression and its application to elucidating negative feedback regulation.
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.
Genetics. 1955 Jul;40(4):511-8. doi: 10.1093/genetics/40.4.511.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验