Temperli E, Roos U P, Hohl H R
Institute of Plant Biology, University of Zürich, Switzerland.
Eur J Cell Biol. 1990 Oct;53(1):75-88.
Actin and tubulins of Phytophthora infestans germlings were detected with monoclonal antibodies on Western blots of crude extracts separated by one-dimensional sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The Mr of actin was approximately 43,000, whereas alpha- and beta-tubulin, which migrated as a single band, had an Mr of 53,000. Rhodamine-phalloin revealed peripheral patches of actin in ungerminated cysts. In young germlings, actin fibers were visible in the conversion zone between cyst and germ tube and as connections between actin patches and the incipient germ tube. Actin patches also occurred throughout the peripheral cytoplasm of longer germ tubes, except for the hyphal apex, which commonly contained actin fibers, but actin patches only exceptionally. Associations between patches and fibers were frequent. A monoclonal antibody specific for actin also stained fibers, but in addition it revealed diffuse staining of the apex and fine granular structures, indicative of the presence of G-actin or of single actin filaments. Cysts incubated with a monoclonal antibody against tubulin contained an array of cytoplasmic microtubules (MTs) that arise from a nucleus-associated center. Some of these MTs circumflexed the nucleus, whereas others extended to the cyst periphery. In germ tubes, axially oriented MT bundles extended from the nucleus-associated center into the proximal and distal cytoplasm. Their density was highest near the nucleus, and their number decreased towards the tip, with only a few remaining at the extreme apex. Bundles of MTs were continuous from the nucleus to the subapical region, reaching lengths of up to 20 microns. Ultrastructurally the bundles consisted of as many as 10 MTs. The architecture of the actin and tubulin cytoskeletons in germ tubes of P. infestans bolsters the hypothesis that they maintain the spatial organization of the hyphal protoplast and support or accomplish intrahyphal movements.
利用单克隆抗体,通过一维十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)对致病疫霉萌发管的粗提物进行分离,并在蛋白质免疫印迹上检测肌动蛋白和微管蛋白。肌动蛋白的相对分子质量(Mr)约为43,000,而α-和β-微管蛋白迁移为一条带,其Mr为53,000。罗丹明鬼笔环肽显示未萌发的孢囊中肌动蛋白呈周边斑块状。在幼嫩的萌发管中,肌动蛋白纤维在孢囊和芽管之间的转化区可见,并且作为肌动蛋白斑块与初始芽管之间的连接。肌动蛋白斑块也出现在较长芽管的整个周边细胞质中,但菌丝顶端通常含有肌动蛋白纤维,只有偶尔出现肌动蛋白斑块。斑块与纤维之间的关联很常见。一种对肌动蛋白特异的单克隆抗体也能使纤维染色,但此外它还显示顶端有弥散性染色以及精细的颗粒结构,表明存在G-肌动蛋白或单条肌动蛋白丝。用抗微管蛋白的单克隆抗体孵育的孢囊含有一系列从与细胞核相关的中心发出的细胞质微管(MTs)。其中一些微管环绕细胞核,而其他微管则延伸到孢囊周边。在芽管中,轴向排列的微管束从与细胞核相关的中心延伸到近端和远端细胞质。它们的密度在细胞核附近最高,数量向顶端减少,在极端顶端仅剩下少数。微管束从细胞核到亚顶端区域是连续的,长度可达20微米。超微结构上,这些微管束由多达10条微管组成。致病疫霉芽管中肌动蛋白和微管蛋白细胞骨架的结构支持了这样的假说,即它们维持菌丝原生质体的空间组织,并支持或完成菌丝内的运动。