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粗糙脉孢菌plc-1、splA2和cpe-1在调节胞质游离钙、类胡萝卜素积累、应激反应和耐热性获得中的多种细胞作用。

Multiple cellular roles of Neurospora crassa plc-1, splA2, and cpe-1 in regulation of cytosolic free calcium, carotenoid accumulation, stress responses, and acquisition of thermotolerance.

作者信息

Barman Ananya, Tamuli Ranjan

机构信息

Department of Biotechnology, Indian Institute of Technology Guwahati, Guwahati, 781 039, India.

出版信息

J Microbiol. 2015 Apr;53(4):226-35. doi: 10.1007/s12275-015-4465-1. Epub 2015 Jan 31.

Abstract

Phospholipase C1 (PLC1), secretory phospholipase A2 (sPLA2) and Ca(2+)/H(+) exchanger proteins regulate calcium signaling and homeostasis in eukaryotes. In this study, we investigate functions for phospholipase C1 (plc-1), sPLA2 (splA2) and a Ca(2+)/H(+) exchanger (cpe-1) in the filamentous fungus Neurospora crassa. The Δplc-1, ΔsplA2, and Δcpe-1 mutants exhibited a growth defect on medium supplemented with the divalent ionophore A23187, suggesting that these genes might play a role in regulation of cytosolic free Ca(2+) concentration (Ca(2+)) in N. crassa. The strains lacking plc-1, splA2, and cpe-1 possessed higher carotenoid content than wild type at 8°C, 22°C, and 30°C, and showed increased ultraviolet (UV)-survival under conditions that induced carotenoid accumulation. Moreover, Δplc-1, ΔsplA2, and Δcpe-1 mutants showed reduced survival rate under hydrogen peroxide-induced oxidative stress and induced thermotolerance after exposure to heat shock temperatures. Thus, this study revealed multiple cellular roles for plc-1, splA2, and cpe-1 genes in regulation of Ca(2+), carotenoid accumulation, survival under stress conditions, and acquisition of thermotolerance induced by heat shock.

摘要

磷脂酶C1(PLC1)、分泌型磷脂酶A2(sPLA2)和Ca(2+)/H(+)交换蛋白调节真核生物中的钙信号传导和体内平衡。在本研究中,我们研究了丝状真菌粗糙脉孢菌中磷脂酶C1(plc-1)、sPLA2(splA2)和Ca(2+)/H(+)交换蛋白(cpe-1)的功能。Δplc-1、ΔsplA2和Δcpe-1突变体在添加二价离子载体A23187的培养基上表现出生长缺陷,这表明这些基因可能在粗糙脉孢菌胞质游离Ca(2+)浓度([Ca(2+)]c)的调节中发挥作用。在8°C、22°C和30°C时,缺乏plc-1、splA2和cpe-1的菌株比野生型具有更高的类胡萝卜素含量,并且在诱导类胡萝卜素积累的条件下表现出紫外线(UV)存活率增加。此外,Δplc-1、ΔsplA2和Δcpe-1突变体在过氧化氢诱导的氧化应激下存活率降低,在暴露于热休克温度后诱导耐热性增加。因此,本研究揭示了plc-1、splA2和cpe-1基因在[Ca(2+)]c调节、类胡萝卜素积累、应激条件下的存活以及热休克诱导的耐热性获得中的多种细胞作用。

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