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首页> 外文期刊>Fungal Genetics and Biology >G protein-cAMP signaling pathway mediated by PGA3 plays different roles in regulating the expressions of amylases and cellulases in Penicillium decumbens
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G protein-cAMP signaling pathway mediated by PGA3 plays different roles in regulating the expressions of amylases and cellulases in Penicillium decumbens

机译:PGA3介导的G蛋白-cAMP信号通路在调节青枯菌中淀粉酶和纤维素酶的表达中发挥不同的作用

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Heterotrimeric G proteins (G proteins) have been extensively investigated for their regulatory functions in morphogenesis and development in filamentous fungi. In addition, G proteins were also shown to be involved in the regulation of cellulase expression in some fungi. Here, we report the different regulatory effects of PGA3, a group III G protein alpha subunit, on the expressions of amylases and cellulases in Penicillium decumbens. Deletion of pga3 resulted in impaired amylase production and significantly decreased transcription of the major amylase gene amy15A. Supplementation of exogenous cAMP or its analog dibutyryl-cAMP restored amylase production in Delta pga3 strain, suggesting an essential role of PGA3 in amylase synthesis via controlling cAMP level. On the other hand, the transcription of major cellulase gene cel7A-2 increased, nevertheless cellulase activity in the medium was not affected, in Delta pga3. The above regulatory effects of PGA3 are carbon source-independent, and are achieved, at least, by cAMP-mediated regulation of the expression level of transcription factor AmyR. The functions of PGA3 revealed by gene deletion were partially supported by the analysis of the mutant carrying dominantly-activated PGA3. The results provided new insights into the understanding of the physiological functions of G protein-cAMP pathway in filamentous fungi
机译:已经广泛研究了异三聚体G蛋白(G蛋白)在丝状真菌的形态发生和发育中的调控功能。另外,还显示了G蛋白参与某些真菌中纤维素酶表达的调节。在这里,我们报告PGA3,第III组G蛋白α亚基,对枯草青霉淀粉酶和纤维素酶表达的不同调节作用。 pga3的删除导致受损的淀粉酶生产和主要淀粉酶基因amy15A的转录明显减少。补充外源性cAMP或其类似物二丁酰-cAMP可恢复Delta pga3菌株中的淀粉酶生产,这表明PGA3在通过控制cAMP水平而在淀粉酶合成中具有重要作用。另一方面,在Delta pga3中,主要的纤维素酶基因cel7A-2的转录增加,但是培养基中的纤维素酶活性没有受到影响。 PGA3的上述调节作用与碳源无关,并且至少通过cAMP介导的转录因子AmyR表达水平的调节来实现。通过基因缺失揭示的PGA3的功能部分通过分析携带显性激活的PGA3的突变体得到支持。该结果为了解丝状真菌G蛋白-cAMP途径的生理功能提供了新的见解。

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