Schoppmeier J, Lechtreck K-F
Botanisches Institut, Universität zu Köln, Cologne, Republic of Germany.
Protoplasma. 2002 Oct;220(1-2):29-38. doi: 10.1007/s00709-002-0031-x.
Recently, p210 was identified as a component of the flagellar basal apparatus in the green flagellate Spermatozopsis similis. In a search for potential homologues to p210, isolated cytoskeletons of several green flagellates were probed with a monoclonal antibody, BAS4.13, against p210. In Western blots, cross-reacting bands in the molecular-mass range of 210 kDa were detected only in the quadriflagellate Spermatozopsis exsultans. As described earlier for S. similis, the flagellar transition region was decorated in Chlamydomonas reinhardtii and several other green flagellates, whereas in the marine alga Dunaliella bioculata the antigen was present in the proximal part of the axoneme. Double immunofluorescence of D. bioculata with an antitubulin antibody further revealed dotlike signals at sites where the probasal bodies are located. Since most of the antigen in D. bioculata was located in the axoneme, deflagellation offered a possibility to study the kinetics of its incorporation during flagellar regeneration. The antigen was only detected after a flagellum reached a length of 3-4 microm and its integration into the growing flagellar proceeded from proximal to distal. A similar delay in the incorporation of the antigen was also observed during flagellar assembly on new basal bodies during cell division. Thus, the antigen of BAS4.13 was incorporated late and from proximal to distal into the growing flagellum. We conclude that the pace and site by which individual proteins are integrated into the flagellum differ greatly.
最近,p210被鉴定为绿藻精子藻(Spermatozopsis similis)鞭毛基部装置的一个组成部分。为了寻找p210的潜在同源物,用抗p210的单克隆抗体BAS4.13对几种绿藻分离出的细胞骨架进行检测。在蛋白质免疫印迹中,仅在四鞭毛的精子藻(Spermatozopsis exsultans)中检测到分子量在210 kDa范围内的交叉反应条带。如先前对相似精子藻(S. similis)的描述,莱茵衣藻(Chlamydomonas reinhardtii)和其他几种绿藻的鞭毛过渡区有该蛋白,而在海洋藻类杜氏盐藻(Dunaliella bioculata)中,抗原存在于轴丝的近端部分。用抗微管蛋白抗体对杜氏盐藻(D. bioculata)进行双重免疫荧光检测,进一步揭示了原基体所在位置的点状信号。由于杜氏盐藻(D. bioculata)中的大部分抗原位于轴丝中,去鞭毛作用为研究其在鞭毛再生过程中的掺入动力学提供了可能。仅在鞭毛达到3 - 4微米长后才能检测到抗原,并且其整合到生长中的鞭毛的过程是从近端向远端进行的。在细胞分裂期间新基体上的鞭毛组装过程中,也观察到抗原掺入的类似延迟。因此,BAS4.13的抗原掺入较晚,且从近端到远端整合到生长中的鞭毛中。我们得出结论,各个蛋白质整合到鞭毛中的速度和位点差异很大。