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本文引用的文献

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Protein O-mannosylation.蛋白质O-甘露糖基化。
Biochim Biophys Acta. 1999 Jan 6;1426(2):297-307. doi: 10.1016/s0304-4165(98)00131-7.
2
A screen for upstream components of the yeast protein kinase C signal transduction pathway identifies the product of the SLG1 gene.一项针对酵母蛋白激酶C信号转导途径上游组分的筛选鉴定出了SLG1基因的产物。
Mol Gen Genet. 1998 Apr;258(1-2):148-55. doi: 10.1007/s004380050717.
3
Temperature-induced expression of yeast FKS2 is under the dual control of protein kinase C and calcineurin.温度诱导的酵母FKS2表达受蛋白激酶C和钙调神经磷酸酶的双重调控。
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4
A family of genes required for maintenance of cell wall integrity and for the stress response in Saccharomyces cerevisiae.酿酒酵母中维持细胞壁完整性和应激反应所需的一个基因家族。
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5
Coordination of the mating and cell integrity mitogen-activated protein kinase pathways in Saccharomyces cerevisiae.酿酒酵母中交配与细胞完整性促分裂原活化蛋白激酶途径的协调。
Mol Cell Biol. 1997 Nov;17(11):6517-25. doi: 10.1128/MCB.17.11.6517.
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A role for the Pkc1 MAP kinase pathway of Saccharomyces cerevisiae in bud emergence and identification of a putative upstream regulator.酿酒酵母的Pkc1丝裂原活化蛋白激酶途径在芽出现中的作用及一个假定上游调节因子的鉴定。
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7
Saccharomyces cerevisiae Mpt5p interacts with Sst2p and plays roles in pheromone sensitivity and recovery from pheromone arrest.酿酒酵母Mpt5p与Sst2p相互作用,并在信息素敏感性及从信息素阻滞中恢复过程中发挥作用。
Mol Cell Biol. 1997 Jun;17(6):3429-39. doi: 10.1128/MCB.17.6.3429.
8
A downstream target of RHO1 small GTP-binding protein is PKC1, a homolog of protein kinase C, which leads to activation of the MAP kinase cascade in Saccharomyces cerevisiae.RHO1小GTP结合蛋白的一个下游靶点是PKC1,它是蛋白激酶C的同源物,可导致酿酒酵母中MAP激酶级联反应的激活。
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9
Activation of yeast protein kinase C by Rho1 GTPase.Rho1 GTP酶对酵母蛋白激酶C的激活作用。
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Dynamics and organization of MAP kinase signal pathways.丝裂原活化蛋白激酶信号通路的动力学与组织架构
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Mid2是酿酒酵母中细胞完整性信号传导的一种假定传感器。

Mid2 is a putative sensor for cell integrity signaling in Saccharomyces cerevisiae.

作者信息

Rajavel M, Philip B, Buehrer B M, Errede B, Levin D E

机构信息

Department of Biochemistry, School of Public Health, The Johns Hopkins University, Baltimore, Maryland 21205, USA.

出版信息

Mol Cell Biol. 1999 Jun;19(6):3969-76. doi: 10.1128/MCB.19.6.3969.

DOI:10.1128/MCB.19.6.3969
PMID:10330137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC104356/
Abstract

Hcs77 is a putative cell surface sensor for cell integrity signaling in Saccharomyces cerevisiae. Its loss of function results in cell lysis during growth at elevated temperatures (e.g., 39 degrees C) and impaired signaling to the Mpk1 mitogen-activated protein kinase in response to mild heat shock. We isolated the MID2 gene as a dosage suppressor of the cell lysis defect of an hcs77 null mutant. MID2 encodes a putative membrane protein whose function is required for survival of pheromone treatment. Mid2 possesses properties similar to those of Hcs77, including a single transmembrane domain and a long region that is rich in seryl and threonyl residues. We demonstrate that Mid2 is required for cell integrity signaling in response to pheromone. Additionally, we show that Mid2 and Hcs77 serve a redundant but essential function as cell surface sensors for cell integrity signaling during vegetative growth. Both proteins are uniformly distributed through the plasma membrane and are highly O-mannosylated on their extracellular domains. Finally, we identified a yeast homolog of MID2, designated MTL1, which provides a partially redundant function with MID2 for cell integrity signaling during vegetative growth at elevated temperature but not for survival of pheromone treatment. We conclude that Hcs77 is dedicated to signaling cell wall stress during vegetative growth and that Mid2 participates in this signaling, but its primary role is in signaling wall stress during pheromone-induced morphogenesis.

摘要

Hcs77是酿酒酵母中一种假定的用于细胞完整性信号传导的细胞表面传感器。其功能丧失会导致在高温(如39摄氏度)下生长时细胞裂解,并削弱在轻度热休克反应中向Mpk1丝裂原活化蛋白激酶的信号传导。我们分离出MID2基因作为hcs77缺失突变体细胞裂解缺陷的剂量抑制因子。MID2编码一种假定的膜蛋白,其功能是信息素处理存活所必需的。Mid2具有与Hcs77相似的特性,包括一个单一的跨膜结构域和一个富含丝氨酸和苏氨酸残基的长区域。我们证明Mid2是信息素诱导的细胞完整性信号传导所必需的。此外,我们表明Mid2和Hcs77在营养生长期间作为细胞完整性信号传导的细胞表面传感器发挥冗余但必不可少的功能。这两种蛋白质均匀分布在质膜中,并且在其细胞外结构域上高度O-甘露糖基化。最后,我们鉴定出MID2的酵母同源物,命名为MTL1,它在高温下营养生长期间为细胞完整性信号传导提供与MID2部分冗余的功能,但对信息素处理的存活不是必需的。我们得出结论,Hcs77在营养生长期间专门用于信号传导细胞壁应激,而Mid2参与这种信号传导,但其主要作用是在信息素诱导的形态发生过程中信号传导细胞壁应激。