Reyes Guadalupe, Romans Angela, Nguyen C Kim, May Gregory S
Division of Pathology and Laboratory Medicine, Unit 54, the University of Texas M D Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.
Eukaryot Cell. 2006 Nov;5(11):1934-40. doi: 10.1128/EC.00178-06. Epub 2006 Sep 22.
The genome of Aspergillus fumigatus has four genes that encode mitogen-activated protein kinases (MAPKs), sakA/hogA, mpkA, mpkB, and mpkC. The functions of the MpkB and MpkC MAPKs are unknown for A. fumigatus and the closely related and genetically amenable species Aspergillus nidulans. mpkC deletion mutants of A. fumigatus were made and their phenotypes characterized. The mpkC deletion mutants were viable and had normal conidial germination and hyphal growth on minimal or complete media. This is in contrast to deletion mutants with deletions in the closely related MAPK gene sakA/hogA that we previously reported had a nitrogen source-dependent germination phenotype. Similarly, the growth of the mpkC deletion mutants was wild type on high-osmolarity medium. Consistent with these two MAP kinase genes regulating different cellular responses, we determined that the mpkC deletion mutants were unable to grow on minimal medium with sorbitol or mannitol as the sole carbon source. This result implicates MpkC signaling in carbon source utilization. Changes in mRNA levels for sakA and mpkC were measured in response to hypertonic stress, oxidative stress, and a shift from glucose to sorbitol to determine if there was overlap in the SakA and MpkC signaling pathways. These studies demonstrated that SakA- and MpkC-dependent patterns of change in mRNA levels are distinct and have minimal overlap in response to these environmental stresses.
烟曲霉的基因组中有四个基因编码丝裂原活化蛋白激酶(MAPK),即sakA/hogA、mpkA、mpkB和mpkC。对于烟曲霉以及与之密切相关且易于进行基因操作的构巢曲霉而言,MpkB和MpkC MAPK的功能尚不清楚。构建了烟曲霉的mpkC缺失突变体并对其表型进行了表征。mpkC缺失突变体能够存活,在基本培养基或完全培养基上具有正常的分生孢子萌发和菌丝生长。这与我们之前报道的在密切相关的MAPK基因sakA/hogA中存在缺失的缺失突变体形成对比,后者具有氮源依赖性萌发表型。同样,mpkC缺失突变体在高渗培养基上的生长为野生型。鉴于这两个MAP激酶基因调节不同的细胞反应,我们确定mpkC缺失突变体无法在以山梨醇或甘露醇作为唯一碳源的基本培养基上生长。这一结果表明MpkC信号传导参与碳源利用。测定了sakA和mpkC的mRNA水平在高渗应激、氧化应激以及从葡萄糖转换为山梨醇时的变化,以确定SakA和MpkC信号通路是否存在重叠。这些研究表明,SakA和MpkC依赖性的mRNA水平变化模式是不同的,在对这些环境应激的反应中重叠极少。