Brock Debra A, Hatton R Diane, Giurgiutiu Dan-Victor, Scott Brenton, Jang Wonhee, Ammann Robin, Gomer Richard H
Howard Hughes Medical Institute, Rice University, Houston, Texas 77005-1892, USA.
Eukaryot Cell. 2003 Aug;2(4):788-97. doi: 10.1128/EC.2.4.788-797.2003.
Developing Dictyostelium cells aggregate to form fruiting bodies containing typically 2 x 10(4) cells. To prevent the formation of an excessively large fruiting body, streams of aggregating cells break up into groups if there are too many cells. The breakup is regulated by a secreted complex of polypeptides called counting factor (CF). Countin and CF50 are two of the components of CF. Disrupting the expression of either of these proteins results in cells secreting very little detectable CF activity, and as a result, aggregation streams remain intact and form large fruiting bodies, which invariably collapse. We find that disrupting the gene encoding a third protein present in crude CF, CF45-1, also results in the formation of large groups when cells are grown with bacteria on agar plates and then starve. However, unlike countin(-) and cf50(-) cells, cf45-1(-) cells sometimes form smaller groups than wild-type cells when the cells are starved on filter pads. The predicted amino acid sequence of CF45-1 has some similarity to that of lysozyme, but recombinant CF45-1 has no detectable lysozyme activity. In the exudates from starved cells, CF45-1 is present in a approximately 450-kDa fraction that also contains countin and CF50, suggesting that it is part of a complex. Recombinant CF45-1 decreases group size in colonies of cf45-1(-) cells with a 50% effective concentration (EC(50)) of approximately 8 ng/ml and in colonies of wild-type and cf50(-) cells with an EC(50) of approximately 40 ng/ml. Like countin(-) and cf50(-) cells, cf45-1(-) cells have high levels of cytosolic glucose, high cell-cell adhesion, and low cell motility. Together, the data suggest that CF45-1 participates in group size regulation in Dictyostelium.
发育中的盘基网柄菌细胞聚集形成通常含有2×10⁴个细胞的子实体。为防止形成过大的子实体,如果细胞过多,聚集细胞流会分裂成多个群体。这种分裂由一种名为计数因子(CF)的分泌型多肽复合物调节。计数蛋白和CF50是CF的两个组成成分。破坏这两种蛋白质中任何一种的表达都会导致细胞分泌的可检测到的CF活性极少,结果,聚集流保持完整并形成大的子实体,而这些子实体总是会坍塌。我们发现,破坏编码粗制CF中存在的第三种蛋白质CF45-1的基因,当细胞在琼脂平板上与细菌一起生长然后饥饿时,也会导致形成大的群体。然而,与计数蛋白缺失型(countin⁻)和CF50缺失型(cf50⁻)细胞不同,当细胞在滤垫上饥饿时,CF45-1缺失型(cf45-1⁻)细胞有时形成的群体比野生型细胞小。CF45-1的预测氨基酸序列与溶菌酶的序列有一些相似性,但重组CF45-1没有可检测到的溶菌酶活性。在饥饿细胞的渗出物中,CF45-1存在于一个约450 kDa的组分中,该组分也含有计数蛋白和CF50,这表明它是一个复合物的一部分。重组CF45-1可减小CF45-1缺失型细胞菌落中的群体大小,其50%有效浓度(EC₅₀)约为8 ng/ml,在野生型和CF50缺失型细胞菌落中的EC₅₀约为40 ng/ml。与计数蛋白缺失型和CF50缺失型细胞一样,CF45-1缺失型细胞具有高水平的胞质葡萄糖、高细胞间粘附性和低细胞运动性。这些数据共同表明,CF45-1参与了盘基网柄菌中群体大小的调节。