Department of Agricultural Science, Kinki University, Nakamachi 3327-204, Nara, 631-8505, Japan.
Kyushu Research Center, Forest Products Research Institute, Kurokami 4-11-16, Kumamoto, 860-0862, Japan.
Arch Microbiol. 2022 Sep 5;204(10):602. doi: 10.1007/s00203-022-03206-z.
The cDNA library prepared from Lentinula edodes, Hokken 600 (H600), primordia was screened using cDNA expressed specifically in Dictyostelium discoideum prestalk as a probe. Twenty-one clones, Le-Dd1 ~ 21, were isolated from the L. edodes primordia cDNA library. Functional analysis of each gene was carried out by transformation into protoplast cells from L. edodes Mori 252 (M252) mycelia with the overexpression vector pLG-RasF1 of each gene because M252 protoplast cells were transformed with an 11-fold higher efficiency than H600 cells. Transformants with the overexpression vector of Le-Dd10 formed a fruiting body at almost the same time as H600, a positive control, although M252, a negative control, did not form a fruiting body under culture conditions. This suggested that Le-Dd10 is involved in the formation of fruiting bodies. Single-strand conformation polymorphism analysis revealed that Le-Dd10 is located on No. 4 linkage group of L. edodes. The properties of Le-Dd10 products were investigated by Western blotting analysis using polyclonal antibodies against GST:Le-Dd10 fusion proteins. As a result, 56-kDa, 27-kDa, and 14-kDa protein bands appeared in primordial and fruiting body stages, although the expected molecular weight of the Le-Dd10 product was 50 kDa.
利用专一地在 Dictyostelium discoideum 前柄中表达的 cDNA 作为探针,从香菇 Hokken 600(H600)原基制备的 cDNA 文库进行筛选。从香菇原基 cDNA 文库中分离出 21 个克隆,Le-Dd1~21。通过将每个基因的过表达载体 pLG-RasF1 转化到香菇 Mori 252(M252)菌丝体的原生质体细胞中,对每个基因的功能进行了分析,因为 M252 原生质体细胞的转化效率比 H600 细胞高 11 倍。在用过表达载体转化的转化体中 Le-Dd10 与阳性对照 H600 几乎同时形成子实体,尽管阴性对照 M252 在培养条件下未形成子实体。这表明 Le-Dd10 参与了子实体的形成。单链构象多态性分析表明 Le-Dd10 位于香菇第 4 号连锁群上。通过使用针对 GST:Le-Dd10 融合蛋白的多克隆抗体进行 Western 印迹分析,研究了 Le-Dd10 产物的特性。结果,在原基和子实体阶段出现了 56-kDa、27-kDa 和 14-kDa 蛋白条带,尽管 Le-Dd10 产物的预期分子量为 50 kDa。