Jin Feng Jie, Takahashi Tadashi, Matsushima Ken-ichiro, Hara Seiichi, Shinohara Yasutomo, Maruyama Jun-ichi, Kitamoto Katsuhiko, Koyama Yasuji
Noda Institute for Scientific Research, 399 Noda, Noda City, Japan.
Eukaryot Cell. 2011 Jul;10(7):945-55. doi: 10.1128/EC.00013-11. Epub 2011 May 6.
Most known basic-region helix-loop-helix (bHLH) proteins belong to a superfamily of transcription factors often involved in the control of growth and differentiation. Therefore, inappropriate expression of genes encoding bHLH proteins is frequently associated with developmental dysfunction. In our previously reported study, a novel bHLH protein-encoding gene (AO090011000215) of Aspergillus oryzae was identified. The gene-disrupted strain was found to produce dense conidia, but sparse sclerotia, relative to the parent strain. Here, to further analyze its function, we generated an overexpressing strain using the A. oryzae amyB gene promoter. Genetic overexpression led to a large number of initial hyphal aggregations and then the formation of mature sclerotia; it was therefore designated sclR (sclerotium regulator). At the same time, the sclR-overexpressing strain also displayed both delayed and decreased conidiation. Scanning electron microscopy indicated that the aerial hyphae of the sclR-overexpressing strain were extremely branched and intertwined with each other. In the generation of the SclR-enhanced green fluorescent protein (EGFP) expression strain, the SclR-EGFP protein fusion was conditionally detected in the nuclei. In addition, the loss of sclR function led to rapid protein degradation and cell lysis in dextrin-polypeptone-yeast extract liquid medium. Taken together, these observations indicate that SclR plays an important role in hyphal morphology, asexual conidiospore formation, and the promotion of sclerotial production, even retaining normal cell function, at least in submerged liquid culture.
大多数已知的碱性区域螺旋-环-螺旋(bHLH)蛋白属于一个转录因子超家族,常参与生长和分化的调控。因此,编码bHLH蛋白的基因表达异常常常与发育功能障碍相关。在我们之前报道的研究中,鉴定出了米曲霉的一个新的编码bHLH蛋白的基因(AO090011000215)。相对于亲本菌株,发现该基因敲除菌株产生密集的分生孢子,但菌核稀疏。在此,为了进一步分析其功能,我们使用米曲霉amyB基因启动子构建了一个过表达菌株。基因过表达导致大量初始菌丝聚集,随后形成成熟菌核;因此将其命名为sclR(菌核调节因子)。同时,sclR过表达菌株的分生孢子形成也出现延迟且数量减少。扫描电子显微镜显示,sclR过表达菌株的气生菌丝极度分支且相互缠绕。在构建SclR-增强绿色荧光蛋白(EGFP)表达菌株时,在细胞核中可检测到SclR-EGFP蛋白融合体。此外,在糊精-蛋白胨-酵母提取物液体培养基中,sclR功能缺失导致蛋白质快速降解和细胞裂解。综上所述,这些观察结果表明,SclR在菌丝形态、无性分生孢子形成以及菌核产生的促进过程中发挥重要作用,至少在深层液体培养中能维持正常细胞功能。