Department of Biology, Graduate School of Science, Osaka City University, Osaka, Japan.
PLoS One. 2013 Jul 16;8(7):e69491. doi: 10.1371/journal.pone.0069491. Print 2013.
Mating pheromone signaling is essential for conjugation between haploid cells of P-type (P-cells) and haploid cells of M-type (M-cells) in Schizosaccharomyces pombe. A peptide pheromone, M-factor, produced by M-cells is recognized by the receptor of P-cells. An M-factor-less mutant, in which the M-factor-encoding genes are deleted, is completely sterile. In liquid culture, sexual agglutination was not observed in the mutant, but it could be recovered by adding exogenous synthetic M-factor, which stimulated expression of the P-type-specific cell adhesion protein, Map4. Exogenous M-factor, however, failed to recover the cell fusion defect in the M-factor-less mutant. When M-factor-less cells were added to a mixture of wild-type P- and M-cells, marked cell aggregates were formed. Notably, M-factor-less mutant cells were also incorporated in these aggregates. In this mixed culture, P-cells conjugated preferentially with M-cells secreting M-factor, and rarely with M-factor-less M-cells. The kinetics of mating parameters in liquid culture revealed that polarized growth commenced from the contact region of opposite mating-type cells. Taken together, these findings indicate that M-factor at a low concentration induces adhesin expression, leading to initial cell-cell adhesion in a type of "distal pheromone action", but M-factor that is secreted directly in the proximity of the adhered P-cells may be necessary for cell fusion in a type of "proximal pheromone action".
交配信息素信号对于 P 型(P 细胞)和 M 型(M 细胞)单倍体细胞之间的接合是至关重要的。M 细胞产生的肽信息素 M 因子被 P 细胞的受体识别。一种 M 因子缺失突变体,其中编码 M 因子的基因被删除,完全不育。在液体培养中,突变体中没有观察到性聚集,但是可以通过添加外源合成的 M 因子来恢复,M 因子刺激 P 型特异性细胞粘附蛋白 Map4 的表达。然而,外源性 M 因子未能恢复 M 因子缺失突变体中的细胞融合缺陷。当 M 因子缺失细胞被添加到野生型 P 和 M 细胞的混合物中时,形成了标记的细胞聚集体。值得注意的是,M 因子缺失突变体细胞也被包含在这些聚集体中。在这种混合培养中,P 细胞优先与分泌 M 因子的 M 细胞接合,而很少与 M 因子缺失的 M 细胞接合。液体培养中交配参数的动力学表明,极化生长始于相反交配型细胞的接触区域。综上所述,这些发现表明,低浓度的 M 因子诱导粘附素的表达,导致初始的细胞间粘附在一种“远端信息素作用”中,但在附着的 P 细胞附近直接分泌的 M 因子可能是细胞融合所必需的在一种“近端信息素作用”中。