Suppr超能文献

酵母1,3-β-D-葡聚糖合酶两个同源亚基的差异表达与功能

Differential expression and function of two homologous subunits of yeast 1,3-beta-D-glucan synthase.

作者信息

Mazur P, Morin N, Baginsky W, el-Sherbeini M, Clemas J A, Nielsen J B, Foor F

机构信息

Merck Research Laboratories, Rahway, New Jersey 07065, USA.

出版信息

Mol Cell Biol. 1995 Oct;15(10):5671-81. doi: 10.1128/MCB.15.10.5671.

Abstract

1,3-beta-D-Glucan is a major structural polymer of yeast and fungal cell walls and is synthesized from UDP-glucose by the multisubunit enzyme 1,3-beta-D-glucan synthase. Previous work has shown that the FKS1 gene encodes a 215-kDa integral membrane protein (Fks1p) which mediates sensitivity to the echinocandin class of antifungal glucan synthase inhibitors and is a subunit of this enzyme. We have cloned and sequenced FKS2, a homolog of FKS1 encoding a 217-kDa integral membrane protein (Fks2p) which is 88% identical to Fks1p. The residual glucan synthase activity present in strains with deletions of fks1 is (i) immunodepleted by antibodies prepared against FKS2 peptides, demonstrating that Fks2p is also a component of the enzyme, and (ii) more sensitive to the echinocandin L-733,560, explaining the increased sensitivity of fks1 null mutants to this drug. Simultaneous disruption of FKS1 and FKS2 is lethal, suggesting that Fks1p and Fks2p are alternative subunits with essential overlapping function. Analysis of FKS1 and FKS2 expression reveals that transcription of FKS1 is regulated in the cell cycle and predominates during growth on glucose, while FKS2 is expressed in the absence of glucose. FKS2 is essential for sporulation, a process which occurs during nutritional starvation. FKS2 is induced by the addition of Ca2+ to the growth medium, and this induction is completely dependent on the Ca2+/calmodulin-dependent phosphoprotein phosphatase calcineurin. We have previously shown that growth of fks1 null mutants is highly sensitive to the calcineurin inhibitors FK506 and cyclosporin A. Expression of FKS2 from the heterologous ADH1 promoter results in FK506-resistant growth. Thus, the sensitivity of fks1 mutants to these drugs can be explained by the calcineurin-dependent transcription of FKS2. Moreover, FKS2 is also highly induced in response to pheromone in a calcineurin-dependent manner, suggesting that FKS2 may also play a role in the remodeling of the cell wall during the mating process.

摘要

1,3-β-D-葡聚糖是酵母和真菌细胞壁的主要结构聚合物,由多亚基酶1,3-β-D-葡聚糖合酶从UDP-葡萄糖合成。先前的研究表明,FKS1基因编码一种215 kDa的整合膜蛋白(Fks1p),它介导对棘白菌素类抗真菌葡聚糖合酶抑制剂的敏感性,并且是该酶的一个亚基。我们已经克隆并测序了FKS2,它是FKS1的同源物,编码一种217 kDa的整合膜蛋白(Fks2p),与Fks1p有88%的同一性。在fks1缺失菌株中存在的残余葡聚糖合酶活性:(i)被针对FKS2肽制备的抗体免疫耗尽,表明Fks2p也是该酶的一个组分;(ii)对棘白菌素L-733,560更敏感,这解释了fks1缺失突变体对该药物增加的敏感性。同时破坏FKS1和FKS2是致死的,表明Fks1p和Fks2p是具有基本重叠功能的替代亚基。对FKS1和FKS2表达的分析表明,FKS1的转录在细胞周期中受到调控,并且在葡萄糖上生长时占主导,而FKS2在没有葡萄糖的情况下表达。FKS2对于孢子形成是必需的,孢子形成是在营养饥饿期间发生的一个过程。FKS2通过向生长培养基中添加Ca2+而被诱导,并且这种诱导完全依赖于Ca2+/钙调蛋白依赖性磷蛋白磷酸酶钙调神经磷酸酶。我们先前已经表明,fks1缺失突变体的生长对钙调神经磷酸酶抑制剂FK5分别为06和环孢菌素A高度敏感。从异源ADH1启动子表达FKS2导致对FK506抗性的生长。因此,fks1突变体对这些药物的敏感性可以通过FKS2的钙调神经磷酸酶依赖性转录来解释。此外,FKS2也以钙调神经磷酸酶依赖性方式对信息素高度诱导,表明FKS2在交配过程中可能也在细胞壁重塑中起作用。

相似文献

引用本文的文献

8
Structure of a fungal 1,3-β-glucan synthase.真菌 1,3-β-葡聚糖合酶的结构。
Sci Adv. 2023 Sep 15;9(37):eadh7820. doi: 10.1126/sciadv.adh7820. Epub 2023 Sep 13.

本文引用的文献

8
Predicting the topology of eukaryotic membrane proteins.预测真核生物膜蛋白的拓扑结构。
Eur J Biochem. 1993 May 1;213(3):1333-40. doi: 10.1111/j.1432-1033.1993.tb17885.x.
10
Review: cell wall assembly in yeast.综述:酵母中的细胞壁组装
Yeast. 1994 Jul;10(7):851-69. doi: 10.1002/yea.320100702.

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