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本文引用的文献

1
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.
2
Nitrogen availability and TOR regulate the Snf1 protein kinase in Saccharomyces cerevisiae.氮素有效性和雷帕霉素靶蛋白(TOR)调节酿酒酵母中的Snf1蛋白激酶。
Eukaryot Cell. 2006 Nov;5(11):1831-7. doi: 10.1128/EC.00110-06. Epub 2006 Sep 15.
3
Feedback control of morphogenesis in fungi by aromatic alcohols.芳香醇对真菌形态发生的反馈控制
Genes Dev. 2006 May 1;20(9):1150-61. doi: 10.1101/gad.1411806. Epub 2006 Apr 17.
4
Ammonium permease-based sensing mechanism for rapid ammonium activation of the protein kinase A pathway in yeast.基于铵通透酶的传感机制,用于酵母中蛋白激酶A途径的快速铵激活。
Mol Microbiol. 2006 Mar;59(5):1485-505. doi: 10.1111/j.1365-2958.2005.05043.x.
5
Glucose and sucrose act as agonist and mannose as antagonist ligands of the G protein-coupled receptor Gpr1 in the yeast Saccharomyces cerevisiae.在酿酒酵母中,葡萄糖和蔗糖作为激动剂,而甘露糖作为G蛋白偶联受体Gpr1的拮抗剂配体。
Mol Cell. 2004 Oct 22;16(2):293-9. doi: 10.1016/j.molcel.2004.10.004.
6
Ras and Gpa2 mediate one branch of a redundant glucose signaling pathway in yeast.Ras和Gpa2介导酵母中一条冗余葡萄糖信号通路的一个分支。
PLoS Biol. 2004 May;2(5):E128. doi: 10.1371/journal.pbio.0020128. Epub 2004 May 11.
7
Genetic and epigenetic regulation of the FLO gene family generates cell-surface variation in yeast.FLO基因家族的遗传和表观遗传调控在酵母中产生细胞表面变异。
Cell. 2004 Feb 6;116(3):405-15. doi: 10.1016/s0092-8674(04)00118-7.
8
Sip2, an N-myristoylated beta subunit of Snf1 kinase, regulates aging in Saccharomyces cerevisiae by affecting cellular histone kinase activity, recombination at rDNA loci, and silencing.Sip2是Snf1激酶的一个N-肉豆蔻酰化β亚基,它通过影响细胞组蛋白激酶活性、rDNA位点的重组和基因沉默来调节酿酒酵母的衰老。
J Biol Chem. 2003 Apr 11;278(15):13390-7. doi: 10.1074/jbc.M212818200. Epub 2003 Jan 31.
9
Snf1 protein kinase and the repressors Nrg1 and Nrg2 regulate FLO11, haploid invasive growth, and diploid pseudohyphal differentiation.Snf1蛋白激酶以及阻遏物Nrg1和Nrg2调节FLO11、单倍体侵袭性生长和二倍体假菌丝分化。
Mol Cell Biol. 2002 Jun;22(12):3994-4000. doi: 10.1128/MCB.22.12.3994-4000.2002.
10
Snf1--a histone kinase that works in concert with the histone acetyltransferase Gcn5 to regulate transcription.Snf1——一种组蛋白激酶,与组蛋白乙酰转移酶Gcn5协同作用以调节转录。
Science. 2001 Aug 10;293(5532):1142-6. doi: 10.1126/science.1062322.

环磷酸腺苷 - 蛋白激酶A和Snf1信号传导机制是蔗糖在酿酒酵母中诱导菌丝形成时具有更高效力的基础。

Cyclic AMP-protein kinase A and Snf1 signaling mechanisms underlie the superior potency of sucrose for induction of filamentation in Saccharomyces cerevisiae.

作者信息

Van de Velde Sam, Thevelein Johan M

机构信息

Laboratory of Molecular Cell Biology, Institute of Botany and Microbiology, Katholieke Universiteit Leuven, and Department ofMolecular Microbiology, VIB, Kasteelpark Arenberg 31, B-3001 Leuven-Heverlee, Flanders, Belgium.

出版信息

Eukaryot Cell. 2008 Feb;7(2):286-93. doi: 10.1128/EC.00276-07. Epub 2007 Sep 21.

DOI:10.1128/EC.00276-07
PMID:17890371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2238163/
Abstract

Under specific environmental conditions, the yeast Saccharomyces cerevisiae can undergo a morphological switch to a pseudohyphal growth pattern. Pseudohyphal differentiation is generally studied upon induction by nitrogen limitation in the presence of glucose. It is known to be controlled by several signaling pathways, including mitogen-activated protein kinase, cyclic AMP-protein kinase A (cAMP-PKA), and Snf1 kinase pathways. We show that the alpha-glucoside sugars maltose and maltotriose, and especially sucrose, are more potent inducers of filamentation than glucose. Sucrose even induces filamentation in nitrogen-rich media and in the mep2Delta/mep2Delta ammonium permease mutant on ammonium-limiting medium. We demonstrate that glucose also inhibits filamentation by means of a pathway parallel to the cAMP-PKA pathway. Deletion of HXK2 shifted the pseudohyphal growth pattern on glucose to that of sucrose, while deletion of SNF4 abrogated filamentation on both sugars, indicating a negative role of glucose repression and a positive role for Snf1 activity in the control of filamentation. In all strains and in all media, sucrose induction of filamentation is greatly diminished by deletion of the sucrose/glucose-sensing G-protein-coupled receptor Gpr1, whereas it has no effect on induction by maltose and maltotriose. The competence of alpha-glucoside sugars to induce filamentation is reflected in the increased expression of the cell surface flocculin gene FLO11. In addition, sucrose is the only alpha-glucoside sugar capable of rapidly inducing FLO11 expression in a Gpr1-dependent manner, reflecting the sensitivity of Gpr1 for this sugar and its involvement in rapid sucrose signaling. Our study identifies sucrose as the most potent nutrient inducer of pseudohyphal growth and shows that glucose inactivation of Snf1 kinase signaling is responsible for the lower potency of glucose.

摘要

在特定环境条件下,酿酒酵母可经历形态转变,形成假菌丝生长模式。假菌丝分化通常在葡萄糖存在下通过氮限制诱导进行研究。已知其受多种信号通路控制,包括丝裂原活化蛋白激酶、环磷酸腺苷 - 蛋白激酶A(cAMP - PKA)和Snf1激酶通路。我们发现,α - 葡糖苷糖麦芽糖和麦芽三糖,尤其是蔗糖,比葡萄糖更能有效诱导丝状化。蔗糖甚至能在富氮培养基中以及在铵限制培养基上的mep2Delta/mep2Delta铵通透酶突变体中诱导丝状化。我们证明,葡萄糖还通过一条与cAMP - PKA通路平行的途径抑制丝状化。HXK2基因的缺失将葡萄糖上的假菌丝生长模式转变为蔗糖上的模式,而SNF4基因的缺失则消除了两种糖上的丝状化,表明葡萄糖阻遏起负作用,而Snf1活性在丝状化控制中起正作用。在所有菌株和所有培养基中,蔗糖诱导的丝状化因蔗糖/葡萄糖传感G蛋白偶联受体Gpr1的缺失而大大减弱,而对麦芽糖和麦芽三糖诱导无影响。α - 葡糖苷糖诱导丝状化的能力反映在细胞表面絮凝蛋白基因FLO11表达的增加上。此外,蔗糖是唯一能够以Gpr1依赖方式快速诱导FLO11表达的α - 葡糖苷糖,这反映了Gpr1对这种糖的敏感性及其参与快速蔗糖信号传导。我们的研究确定蔗糖是假菌丝生长最有效的营养诱导物,并表明Snf1激酶信号传导的葡萄糖失活是葡萄糖效力较低的原因。