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A basic-region helix-loop-helix protein-encoding gene (devR) involved in the development of Aspergillus nidulans

机译:一个基础区域螺旋-环-螺旋蛋白编码基因(devR)参与构巢曲霉的发展

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Basic-region helix-loop-helix (bHLH) proteins form an interesting class of eukaryotic transcription factors often involved in developmental processes. Here, a so far unknown bHLH protein-encoding gene of the filamentous ascomycete Aspergillus nidulans was isolated and designated devR for regulator of development. Deletion of devR revealed that the gene is non-essential for vegetative growth. However, the deletion mutant produced wrinkled colonies, a yellow pigment and did not form conidia on minimal agar plates. Conidiophore development was initiated normally, and colonies produced conidiophores with metulae and phialides. However, the phialides continued to grow filamentously and produced a second conidiophore with a vesicle at its end. The addition of KCl (0.6 M) to the medium suppressed the knock-out phenotype. The DeltadevR phenotype resembled that of a mutation in the tcsA gene encoding a histidine kinase domain and a response regulator domain. Here, we generated a tcsA deletion mutant. In a DeltatcsA strain, a DevR-Egfp protein fusion was detected in the cytoplasm, whereas in the wild type, the protein fusion was exclusively located in the nuclei, indicating that TcsA is required for nuclear localization of DevR. devR mRNA steady-state levels were similar in sporulating and vegetatively growing mycelia, and independent of a functional brlA gene. Moreover, under all conditions tested, self-crossing of the DeltadevR mutant strain was never observed. Taken together, devR encodes a bHLH regulatory protein that is part of the tcsA signal transduction network and required for development under standard growth conditions. [References: 64]
机译:基本区域螺旋-环-螺旋(bHLH)蛋白形成一类有趣的真核转录因子,通常参与发育过程。在此,分离出迄今未知的丝状囊孢菌nidulans的bHLH蛋白编码基因,并将其指定为发育调节剂devR。 devR的删除表明该基因对于营养生长不是必需的。但是,缺失突变体产生了皱纹的菌落,黄色颜料,并且在最小的琼脂平板上没有形成分生孢子。分生孢子的发育正常开始,菌落产生了带有metulae和phialides的分生孢子。但是,phialides继续长丝状生长,并产生了第二个分生孢子体,其末端有一个囊泡。向培养基中添加KCl(0.6 M)会抑制敲除表型。 DeltadevR表型类似于编码组氨酸激酶域和响应调节域的tcsA基因突变。在这里,我们生成了一个tcsA缺失突变体。在DeltatcsA菌株中,在细胞质中检测到DevR-Egfp蛋白融合体,而在野生型中,蛋白融合体仅位于细胞核中,表明TcsA是DevR的核定位所必需。 devR mRNA稳态水平在孢子形成和营养生长菌丝体中相似,并且独立于功能性brlA基因。此外,在所有测试条件下,从未观察到DeltadevR突变株的自交。总之,devR编码bHLH调节蛋白,该蛋白是tcsA信号转导网络的一部分,并且是在标准生长条件下发育所必需的。 [参考:64]

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