Gomer R H, Datta S, Firtel R A
J Cell Biol. 1986 Nov;103(5):1999-2015. doi: 10.1083/jcb.103.5.1999.
We have analyzed a developmentally and spatially regulated prestalk-specific gene and a prespore-specific gene from Dictyostelium. The prestalk gene, pst-cathepsin, encodes a protein highly homologous to the lysosomal cysteine proteinases cathepsin H and cathepsin B. The prespore gene encodes a protein with some homology to the anti-bacterial toxin crambin and has been designated beejin. Using the lambda gtll system, we have made polyclonal antibodies directed against a portion of the protein encoded by pst-cathepsin and other antibodies directed against the beejin protein. Both antibodies stain single bands on Western blots. By immunofluorescence and Western blots, pst-cathepsin is not present in vegetative cells or developing cells during the first approximately 10 h of development. It then appears with a punctate distribution in a subset of developing cells. Beejin is detected only after approximately 15 h of development, also in a subset of cells. Pst-cathepsin is distributed in the anterior approximately 1/10 of migrating slugs and on the peripheral posterior surfaces of slugs. Beejin is distributed in the posterior region of slugs. Expression of both pst-cathepsin and beejin can be induced in subsets of isolated cultured cells by a combination of conditioned medium and extracellular cAMP in agreement with the regulation of the mRNAs encoding these proteins. We have used the antibodies as markers for cell type to examine the ontogeny and the spatial distribution of prestalk and prespore cells throughout multicellular development. Our findings suggest that prestalk cell differentiation is independent of position within the aggregate and that the spatial localization of prestalk cells within the multicellular aggregate arises from sorting of the prestalk cells after their induction. We have also found a class of cell in developing aggregates that contains neither the prestalk nor the prespore markers.
我们分析了盘基网柄菌中一个在发育和空间上受调控的前柄特异性基因和一个前孢子特异性基因。前柄基因pst - 组织蛋白酶编码一种与溶酶体半胱氨酸蛋白酶组织蛋白酶H和组织蛋白酶B高度同源的蛋白质。前孢子基因编码一种与抗菌毒素胰凝乳蛋白酶原有些同源性的蛋白质,被命名为蜂蛋白。利用λgtll系统,我们制备了针对pst - 组织蛋白酶编码的部分蛋白质的多克隆抗体以及针对蜂蛋白的其他抗体。两种抗体在蛋白质印迹法中均能染出单一条带。通过免疫荧光和蛋白质印迹法检测发现,在发育的最初约10小时内,营养细胞或发育中的细胞中不存在pst - 组织蛋白酶。随后它出现在一部分发育细胞中,呈点状分布。蜂蛋白仅在发育约15小时后在一部分细胞中被检测到。Pst - 组织蛋白酶分布在迁移的蛞蝓前端约1/10处以及蛞蝓的外周后表面。蜂蛋白分布在蛞蝓的后部区域。与编码这些蛋白质的mRNA的调控一致,通过条件培养基和细胞外cAMP的组合,可在分离培养的细胞亚群中诱导pst - 组织蛋白酶和蜂蛋白的表达。我们使用这些抗体作为细胞类型的标志物,来研究前柄和前孢子细胞在整个多细胞发育过程中的个体发育和空间分布。我们的研究结果表明,前柄细胞的分化与聚集体内的位置无关,多细胞聚集体内前柄细胞的空间定位是在前柄细胞诱导后通过分选产生的。我们还在发育中的聚集体中发现了一类既不含有前柄也不含有前孢子标志物的细胞。