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钙调神经磷酸酶,一种Ca2+/钙调蛋白依赖性蛋白磷酸酶,在具有细胞完整性缺陷的酵母突变体以及缺乏功能性液泡H(+)-ATP酶的突变体中至关重要。

Calcineurin, the Ca2+/calmodulin-dependent protein phosphatase, is essential in yeast mutants with cell integrity defects and in mutants that lack a functional vacuolar H(+)-ATPase.

作者信息

Garrett-Engele P, Moilanen B, Cyert M S

机构信息

Department of Biological Sciences, Stanford University, California 94305-5020.

出版信息

Mol Cell Biol. 1995 Aug;15(8):4103-14. doi: 10.1128/MCB.15.8.4103.

Abstract

Calcineurin is a conserved Ca2+/calmodulin-dependent protein phosphatase that plays a critical role in Ca(2+)-mediated signaling in many cells. Yeast cells lacking functional calcineurin (cna1 cna2 or cnb1 mutants) display growth defects under specific environmental conditions, for example, in the presence of high concentrations of Na+, Li+, Mn2+, or OH- but are indistinguishable from wild-type cells under standard culture conditions. To characterize regulatory pathways that may overlap with calcineurin, we performed a synthetic lethal screen to identify mutants that require calcineurin on standard growth media. The characterization of one such mutant, cnd1-8, is presented. The CND1 gene was cloned, and sequence analysis predicts that it encodes a novel protein 1,876 amino acids in length with multiple membrane-spanning domains. CND1 is identical to the gene identified previously as FKS1, ETG1, and CWH53, cnd1 mutants are sensitive to FK506 and cyclosporin A and exhibit slow growth that is improved by the addition of osmotic stabilizing agents. This osmotic agent-remedial growth defect and microscopic evidence of spontaneous cell lysis in cnd1 cultures suggest that cell integrity is compromised in these mutants. Mutations in the genes for yeast protein kinase C (pkc1) and a MAP kinase (mpk1/slt2) disrupt a Ca(2+)-dependent signaling pathway required to maintain a normal cell wall and cell integrity. We show that pkc1 and mpk1/slt2 growth defects are more severe in the absence of calcineurin function and less severe in the presence of a constitutively active form of calcineurin. These observations suggest that calcineurin and protein kinase C perform independent but physiologically related functions in yeast cells. We show that several mutants that lack a functional vacuolar H(+)-ATPase (vma) require calcineurin for vegetative growth. We discuss possible roles for calcineurin in regulating intracellular ion homeostasis and in maintaining cell integrity.

摘要

钙调神经磷酸酶是一种保守的Ca2+/钙调蛋白依赖性蛋白磷酸酶,在许多细胞的Ca(2+)介导的信号传导中起关键作用。缺乏功能性钙调神经磷酸酶的酵母细胞(cna1 cna2或cnb1突变体)在特定环境条件下表现出生长缺陷,例如,在高浓度的Na+、Li+、Mn2+或OH-存在的情况下,但在标准培养条件下与野生型细胞没有区别。为了表征可能与钙调神经磷酸酶重叠的调控途径,我们进行了一项合成致死筛选,以鉴定在标准生长培养基上需要钙调神经磷酸酶的突变体。本文介绍了其中一个这样的突变体cnd1-8的表征。CND1基因被克隆,序列分析预测它编码一种长度为1876个氨基酸的新型蛋白质,具有多个跨膜结构域。CND1与先前鉴定为FKS1、ETG1和CWH53的基因相同,cnd1突变体对FK506和环孢菌素A敏感,并且生长缓慢,添加渗透稳定剂可改善这种情况。这种渗透剂纠正的生长缺陷以及cnd1培养物中自发细胞裂解的显微镜证据表明,这些突变体的细胞完整性受到损害。酵母蛋白激酶C(pkc1)和丝裂原活化蛋白激酶(mpk1/slt2)基因的突变破坏了维持正常细胞壁和细胞完整性所需的Ca(2+)依赖性信号通路。我们表明,在没有钙调神经磷酸酶功能的情况下,pkc1和mpk1/slt2的生长缺陷更严重,而在存在组成型活性形式的钙调神经磷酸酶的情况下则不太严重。这些观察结果表明,钙调神经磷酸酶和蛋白激酶C在酵母细胞中执行独立但生理相关的功能。我们表明,几个缺乏功能性液泡H(+)-ATP酶(vma)的突变体在营养生长中需要钙调神经磷酸酶。我们讨论了钙调神经磷酸酶在调节细胞内离子稳态和维持细胞完整性方面的可能作用。

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