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The function of the three phosphoribosyl pyrophosphate synthetase (Prs) genes in hyphal growth and conidiation in Aspergillus nidulans

机译:构巢曲霉中三个磷酸核糖焦磷酸合成酶(Prs)基因在菌丝生长和分生中的功能

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Phosphoribosyl pyrophosphate synthetase, which is encoded by the Prs gene, catalyses the reaction of ribose-5-phosphate and adenine ribonucleotide triphosphate (ATP) and has central importance in cellular metabolism. However, knowledge about how Prs family members function and contribute to total 5-phosphoribosyl-α-1-pyrophosphate (PRPP) synthetase activity is limited. In this study, we identified that the filamentous fungus Aspergillus nidulans genome contains three PRPP synthase-homologous genes (AnprsA, AnprsB and AnprsC), among which AnprsB and AnprsC but not AnprsA are auxotrophic genes. Transcriptional expression profiles revealed that the mRNA levels of AnprsA, AnprsB and AnprsC are dynamic during germination, hyphal growth and sporulation and that they all showed abundant expression during the vigorous hyphal growth time point. Inhibiting the expression of AnprsB or AnprsC in conditional strains produced more effects on the total PRPP synthetase activity than did inhibiting AnprsA, thus indicating that different AnPrs proteins are unequal in their contributions to Prs enzyme activity. In addition, the constitutive overexpression of AnprsA or AnprsC could significantly rescue the defective phenotype of the AnprsB-absent strain, suggesting that the function of AnprsB is not a specific consequence of this auxotrophic gene but instead comes from the contribution of Prs proteins to PRPP synthetase activity.
机译:由Prs基因编码的磷酸核糖焦磷酸合成酶催化5核糖核糖和三磷酸腺嘌呤核糖核苷酸(ATP)的反应,在细胞代谢中具有重要意义。但是,关于Prs家族成员如何发挥功能并促进总5-磷酸核糖基-α-1-焦磷酸(PRPP)合成酶活性的知识是有限的。在这项研究中,我们确定丝状真菌构巢曲霉基因组包含三个PRPP合酶同源基因(AnprsA,AnprsB和AnprsC),其中AnprsB和AnprsC但不是AnprsA是营养缺陷型基因。转录表达谱显示AnprsA,AnprsB和AnprsC的mRNA水平在发芽,菌丝生长和孢子形成过程中是动态的,并且在有力的菌丝生长时间点均显示出丰富的表达。与抑制AnprsA相比,在条件菌株中抑制AnprsB或AnprsC的表达对总PRPP合成酶活性的影响更大,因此表明不同的AnPrs蛋白对Prs酶活性的贡献是不相等的。另外,AnprsA或AnprsC的组成型过表达可以显着挽救AnprsB缺失菌株的缺陷表型,表明AnprsB的功能不是该营养缺陷型基因的特定结果,而是来自Prs蛋白对PRPP合成酶的贡献活动。

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