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Starvation stress modulates the expression of the Aspergillus nidulans brlA regulatory gene

机译:饥饿胁迫调节Aspergillus Nidulans Brla调节基因的表达

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SUMMARY: Expression of the Aspergillus nidulans brlA gene plays a fundamental role in the switch from vegetative growth to asexual reproduction. Using a media-shifting protocol to induce submerged sporulation and brlA-lacZ as an expression marker, it was shown that carbon and nitrogen starvation stress induced brlA transcription to different degrees. Glucose starvation induced brlA rapidly to high levels and resulted in spore formation on reduced conidiophores, whereas nitrogen starvation induced brlA gradually to lower levels and sporulation occurred to a lesser extent but from more complex conidiophores. β-Galactosidase activity paralleled brlAα and brlAβ mRNA. No clear qualitative differences between the two brlA transcripts were found in these starvation conditions, suggesting that the different patterns of sporulation could be explained by quantitative expression differences. Since brlA mRNA did not accumulate in the presence of a high glucose concentration, we investigated the role of other carbon sources on brlA expression. Non-repressing carbon sources such as glycerol, acetate and arabinose were as effective as glucose in preventing brlA mRNA accumulation, suggesting that the glucose effects on brlA expression could be explained as a response to nutrient starvation, rather than by carbon catabolite repression. Despite similar low levels of brlA transcripts being detected during growth in glucose or non-repressing carbon sources, conidiophores were formed only in medium containing glycerol, acetate or arabinose. When mycelia were not shifted to starvation conditions, sporulation was not observed in standard minimal medium even after glucose was exhausted, unless the medium was buffered. This and other results suggest that strong deviation from external neutral pH partially prevented full induction and/or function of brlA.
机译:发明内容:Aspergillus Nidulans Brla基因的表达在从营养生长到无性繁殖的切换中发挥着重要作用。使用介质转移方案诱导浸没的孢子率和BRLA-LACZ作为表达标记,结果表明碳和氮饥饿应激诱导BR1A转录到不同程度。葡萄糖饥饿迅速诱导BRLA以迅速达到高水平,并导致孢子形成在降低的卵细胞上,而氮饥饿诱导BRLA逐渐降低到较小程度上,但从更复杂的分子中发生较低。 β-半乳糖苷酶活性平行的Brlaα和BrlaβmRNA。在这些饥饿条件下发现两个BR1A转录物之间没有明确的定性差异,表明可以通过定量表达差异来解释不同的孢子模式。由于BRLA mRNA在存在高葡萄糖浓度的情况下没有积累,因此我们研究了其他碳源对BRLA表达的作用。非抑制碳源如甘油,乙酸盐和阿拉伯糖在预防Brla mRNA积累时与葡萄糖有效,这表明可以将对BR1A表达的葡萄糖作用作为对营养饥饿的反应,而不是通过碳分解代谢物抑制来解释。尽管在葡萄糖或非抑制碳源的生长期间检测到类似的BR1A转录物的相似性,但仅在含有甘油,乙酸盐或阿拉伯糖中的培养基中形成分枝体。当菌丝体未移位到饥饿条件时,否则在葡萄糖耗尽后,甚至在标准最小培养基中未观察到孢子,除非培养基被缓冲。其它结果表明,与外中性pH的强烈偏差部分地阻止了BRLA的完全感应和/或功能。

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