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Cellular and subcellular distribution of a cAMP-regulated prestalk protein and prespore protein in Dictyostelium discoideum: a study on the ontogeny of prestalk and prespore cells

机译:盘基网柄菌中cAMP调节的茎前蛋白和芽孢前蛋白在细胞和亚细胞中的分布:茎前细胞和芽前细胞的个体发育研究

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摘要

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.
机译:我们已经分析了一种来自盘基网柄菌的发育和空间调节的茎前特异性基因和芽孢前特异性基因。前茎基因pst-cathepsin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Crambin具有某些同源性的蛋白质。使用lambda gtll系统,我们制备了针对pst-cathepsin编码的一部分蛋白质的多克隆抗体,以及针对beejin蛋白的其他抗体。两种抗体均在Western印迹上染色单条带。通过免疫荧光和蛋白质印迹,在发育的最初约10小时内,营养细胞或发育细胞中不存在pst组织蛋白酶。然后它在发育中的细胞子集中出现点状分布。仅在发育约15小时后,在一个细胞亚群中也检测到Beejin。 Pst-cathepsin分布在迁移的前约1/10以及and的外围后表面。 Beejin分布在的后部。 pst-cathepsin和beejin的表达均可通过条件培养基和细胞外cAMP结合编码这些蛋白的mRNA的调控而在分离的培养细胞亚群中诱导。我们已使用抗体作为细胞类型的标记物来检查整个多细胞发育过程中茎和芽孢细胞的发育和空间分布。我们的发现表明,前茎细胞的分化与聚集物中的位置无关,并且多细胞聚集物中前茎细胞的空间定位是由前茎细胞诱导后的排序产生的。我们还发现了正在发育的聚集体中的一类细胞,既不包含前茎也不包含前孢子标记。

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