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A novel connection between the Cell Wall Integrity and the PKA pathways regulates cell wall stress response in yeast

机译:细胞壁完整性和PKA途径之间的新型联系调节酵母细胞壁的应激反应

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摘要

Fungal cells trigger adaptive mechanisms to survive in situations that compromise cell wall integrity. We show here that the global transcriptional response elicited by inhibition of the synthesis of β-1,3-glucan by caspofungin, encompasses a set of genes that are dependent on Slt2, the MAPK of the Cell Wall Integrity (CWI) pathway, and a broad group of genes regulated independently of Slt2. Genes negatively regulated by the cyclic AMP/Protein Kinase A (PKA) signaling pathway were overrepresented in the latter group. Moreover, cell wall stress mediated by inhibition of β-1,3-glucan synthesis, but not by other cell wall interfering compounds, negatively regulated PKA signaling as indicated by the nuclear localisation of Msn2, cellular glycogen accumulation, a decrease of intracellular cAMP levels and a severe decrease in both the activation of the small GTPase Ras2 and the phosphorylation of known substrates of PKA. All these effects relied on the plasma membrane-spanning sensor of the CWI pathway Wsc1. In addition, caspofungin induced a reduction in the cytosolic pH, which was dependent on the extracellular region of Wsc1. Therefore, alterations of the β-1,3-glucan network in the fungal cell wall, induce, through Wsc1, the activation of the CWI pathway and parallel inhibition of PKA signaling.
机译:真菌细胞触发适应性机制,以在损害细胞壁完整性的情况下存活。我们在这里显示,通过卡泊芬净抑制β-1,3-葡聚糖的合成引起的全球转录反应,包括一组依赖于Slt2的基因,细胞壁完整性(CWI)途径的MAPK和不受Slt2调控的广泛基因。在后一组中,由环状AMP /蛋白激酶A(PKA)信号通路负调控的基因过高。而且,通过抑制β-1,3-葡聚糖合成而不是其他细胞壁干扰化合物介导的细胞壁应激,负调节了PKA信号,如Msn2的核定位,细胞糖原积累,细胞内cAMP水平降低并且小GTPase Ras2的激活和已知PKA底物的磷酸化都大大降低。所有这些作用都依赖于CWI通路Wsc1的质膜跨度传感器。此外,卡泊芬净引起的细胞质pH降低,这取决于Wsc1的细胞外区域。因此,真菌细胞壁中β-1,3-葡聚糖网络的改变通过Wsc1诱导了CWI途径的激活和对PKA信号的平行抑制。

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