Johnson K A, Rosenbaum J L
Department of Biology, Yale University, New Haven, Connecticut 06511.
J Cell Biol. 1992 Dec;119(6):1605-11. doi: 10.1083/jcb.119.6.1605.
During mating of the alga Chlamydomonas, two biflagellate cells fuse to form a single quadriflagellate cell that contains two nuclei and a common cytoplasm. We have used this cell fusion during mating to transfer unassembled flagellar components from the cytoplasm of one Chlamydomonas cell into that of another in order to study in vivo the polarity of flagellar assembly. In the first series of experiments, sites of tubulin addition onto elongating flagellar axonemes were determined. Donor cells that had two full-length flagella and were expressing an epitope-tagged alpha-tubulin construct were mated (fused) with recipient cells that had two half-length flagella. Outgrowth of the shorter pair of flagella followed, using a common pool of precursors that now included epitope-tagged tubulin, resulting in quadriflagellates with four full-length flagella. Immunofluorescence and immunoelectron microscopy using an antiepitope antibody showed that both the outer doublet and central pair microtubules of the recipient cells' flagellar axonemes elongate solely by addition of new subunits at their distal ends. In a separate series of experiments, the polarity of assembly of a class of axonemal microtubule-associated structures, the radial spokes, was determined. Wild-type donor cells that had two full-length, motile flagella were mated with paralyzed recipient cells that had two full-length, radial spokeless flagella. Within 90 min after cell fusion, the previously paralyzed flagella became motile. Immunofluorescence microscopy using specific antiradial spoke protein antisera showed that radial spoke proteins appeared first at the tips of spokeless axonemes and gradually assembled toward the bases. Together, these results suggest that both tubulin and radial spoke proteins are transported to the tip of the flagellum before their assembly into flagellar structure.
在衣藻交配过程中,两个具双鞭毛的细胞融合形成一个单一的具四鞭毛的细胞,该细胞包含两个细胞核和一个共同的细胞质。我们利用交配过程中的这种细胞融合,将未组装的鞭毛成分从一个衣藻细胞的细胞质转移到另一个衣藻细胞的细胞质中,以便在体内研究鞭毛组装的极性。在第一系列实验中,确定了微管蛋白添加到伸长的鞭毛轴丝上的位点。将具有两条全长鞭毛并表达表位标记的α-微管蛋白构建体的供体细胞与具有两条半长鞭毛的受体细胞进行交配(融合)。随后,较短的一对鞭毛生长,利用现在包括表位标记微管蛋白的共同前体池,产生具有四条全长鞭毛的四鞭毛细胞。使用抗表位抗体的免疫荧光和免疫电子显微镜显示,受体细胞鞭毛轴丝的外双联体微管和中央对微管仅通过在其远端添加新的亚基而伸长。在另一系列实验中,确定了一类轴丝微管相关结构——径向辐条的组装极性。具有两条全长可运动鞭毛的野生型供体细胞与具有两条全长、无径向辐条的麻痹受体细胞进行交配融合。细胞融合后90分钟内,先前麻痹的鞭毛变得可运动。使用特异性抗径向辐条蛋白抗血清的免疫荧光显微镜显示,径向辐条蛋白首先出现在无辐条轴丝的尖端,并逐渐向基部组装。这些结果共同表明,微管蛋白和径向辐条蛋白在组装成鞭毛结构之前都被运输到鞭毛的尖端。