Department of Life Science, Chonbuk National University, Chonju 561-756, Republic of Korea.
Fungal Genet Biol. 2013 Dec;61:42-9. doi: 10.1016/j.fgb.2013.09.010. Epub 2013 Oct 22.
The mpkB gene of Aspergillus nidulans encodes a MAP kinase homologous to Fus3p of Saccharomyces cerevisiae which is involved in conjugation process. MpkB is required for completing the sexual development at the anastomosis and post-karyogamy stages. The mpkB deletion strain could produce conidia under the repression condition of conidiation such as sealing and even in the submerged culture concomitant with persistent brlA expression, implying that MpkB might have a role in timely regulation of brlA expression. The submerged culture of the deletion strain showed typical autolytic phenotypes including decrease in dry cell mass (DCM), disorganization of mycelial balls, and fragmentation of hyphae. The chiB, engA and pepJ genes which are encoding cell wall hydrolytic enzymes were transcribed highly in the submerged culture. Also, we observed that the enzyme activity of chitinase and glucanase in the submerged culture of mpkB deletion strain was much higher than that of wild type. The deletion of mpkB also caused a precocious germination of conidia and reduction of spore viability. The expression of the vosA gene, a member of velvet gene family, was not observed in the mpkB deletion strain. These results suggest that MpkB should have multiple roles in germination and viability of conidia, conidiation and autolysis through regulating the expression of vosA and brlA.
粗糙脉孢菌的 mpkB 基因编码一种与酿酒酵母的 Fus3p 同源的 MAP 激酶,该激酶参与了接合过程。MpkB 对于在吻合和核后阶段完成有性发育是必需的。mpkB 缺失株可以在孢子形成的抑制条件下产生分生孢子,例如密封,甚至在伴随持续 brlA 表达的浸没培养中,这表明 MpkB 可能在 brlA 表达的适时调节中发挥作用。缺失株的浸没培养表现出典型的自溶表型,包括干细胞质量(DCM)减少、菌丝球结构紊乱和菌丝断裂。chiB、engA 和 pepJ 基因,编码细胞壁水解酶,在浸没培养中高度转录。此外,我们观察到,mpkB 缺失株的浸没培养中的几丁质酶和葡聚糖酶的酶活性比野生型高得多。mpkB 的缺失也导致分生孢子的早熟萌发和孢子活力的降低。在 mpkB 缺失株中没有观察到 velvet 基因家族成员 vosA 基因的表达。这些结果表明,MpkB 通过调节 vosA 和 brlA 的表达,应该在分生孢子的萌发和活力、孢子形成和自溶方面发挥多种作用。