Kameshita Isamu, Yamada Yusuke, Nishida Tetsuyuki, Sugiyama Yasunori, Sueyoshi Noriyuki, Watanabe Akira, Asada Yasuhiko
Department of Life Sciences, Faculty of Agriculture, Kagawa University, Ikenobe 2393, Miki-cho, Kagawa 761-0795, Japan.
Biochim Biophys Acta. 2007 Sep;1770(9):1395-403. doi: 10.1016/j.bbagen.2007.05.008. Epub 2007 Jun 8.
Although multifunctional Ca(2+)/calmodulin-dependent protein kinases (CaM-kinases) are widely distributed in animal cells, the occurrence of CaM-kinases in the basidiomycetous mushroom has not previously been documented. When the extracts from various developmental stages from mycelia to the mature fruiting body of Coprinus cinereus were analyzed by Western blotting using Multi-PK antibodies, which had been generated to detect a wide variety of protein serine/threonine kinases (Ser/Thr kinases), a variety of stage-specific Ser/Thr kinases was detected. Calmodulin (CaM) overlay assay using digoxigenin-labeled CaM detected protein bands of 65 kDa, 58 kDa, 46 kDa, 42 kDa, and 38 kDa only in the presence of CaCl(2), suggesting that these bands were CaM-binding proteins. When the CaM-binding fraction was prepared from mycelial extract of C. cinereus by CaM-Sepharose and analyzed with Multi-PK antibodies, two major immunoreactive bands corresponding to 65 kDa and 46 kDa were detected. CaM-binding fraction, thus obtained, exhibited Ca(2+)/CaM-dependent protein kinase activity toward protein substrates such as histones. These CaM-kinases were found to be highly expressed in the actively growing mycelia, but not in the resting mycelial cells. Mycelial growth was enhanced by the addition of CaCl(2) in the culture media, but inhibited by the addition of EGTA or trifluoperazine, a potent CaM inhibitor. This suggested that CaM-dependent enzymes including CaM-kinases play crucial roles in mycelial growth of basidiomycete C. cinereus.
尽管多功能钙调蛋白依赖性蛋白激酶(CaM激酶)广泛分布于动物细胞中,但此前尚未有文献记载其在担子菌蘑菇中的存在情况。当使用为检测多种蛋白丝氨酸/苏氨酸激酶(Ser/Thr激酶)而制备的多PK抗体,通过蛋白质印迹法分析灰盖鬼伞从菌丝体到成熟子实体各个发育阶段的提取物时,检测到了多种阶段特异性的Ser/Thr激酶。使用地高辛标记的钙调蛋白(CaM)进行的CaM覆盖分析仅在存在氯化钙(CaCl₂)的情况下检测到了65 kDa、58 kDa、46 kDa、42 kDa和38 kDa的蛋白条带,这表明这些条带是CaM结合蛋白。当通过CaM - 琼脂糖从灰盖鬼伞的菌丝体提取物中制备CaM结合组分并用多PK抗体进行分析时,检测到了对应于65 kDa和46 kDa的两个主要免疫反应条带。由此获得的CaM结合组分对诸如组蛋白等蛋白质底物表现出钙(Ca²⁺)/钙调蛋白依赖性蛋白激酶活性。这些CaM激酶在活跃生长的菌丝体中高度表达,但在静止的菌丝体细胞中不表达。在培养基中添加氯化钙可促进菌丝体生长,但添加乙二醇双乙醚二胺四乙酸(EGTA)或强效CaM抑制剂三氟拉嗪则会抑制菌丝体生长。这表明包括CaM激酶在内的CaM依赖性酶在担子菌灰盖鬼伞的菌丝体生长中起着关键作用。