Kann Marie-Louise, Soues Sylvie, Levilliers Nicolette, Fouquet Jean-Pierre
Laboratoire de Biologie Cellulaire, EA 2508 MENRT, Université Paris V, UFR Biomedicale, 45 rue des Saintes-Pères, 75270 Paris cedex 06, France.
Cell Motil Cytoskeleton. 2003 May;55(1):14-25. doi: 10.1002/cm.10107.
Glutamylation of alpha and beta tubulin isotypes is a major posttranslational modification giving rise to diversified isoforms occurring mainly in neurotubules, centrioles, and axonemes. Monoglutamylated tubulin isoforms can be differentially recognized by two mAbs, B3 and GT335, which both recognize either polyglutamylated isoforms. In the present study, immunoelectron microscopy and immunofluorescence analyses were performed with these two mAbs to determine the expression and distribution of glutamylated tubulin isoforms in selected biological models whose tubulin isotypes are characterized. In mouse spermatozoa, microtubules of the flagellum contain polyglutamylated isoforms except in the tip where only monoglutamylated isoforms are detected. In spermatids, only a subset of manchette microtubules contain monoglutamylated tubulin isoforms. Cytoplasmic microtubules of Sertoli cells are monoglutamylated. Mitotic and meiotic spindles of germ cells are monoglutamylated whereas the HeLa cell mitotic spindle is polyglutamylated. Three models of axonemes are demonstrated as a function of the degree and extent of tubulin glutamylation. In lung ciliated cells, axonemes are uniformly polyglutamylated. In sea urchin sperm and Chlamydomonas, flagellar microtubules are polyglutamylated in their proximal part and monoglutamylated in their distal part. In Paramecium, cilia are bi- or monoglutamylated only at their base. In all cells, centrioles or basal bodies are polyglutamylated. These new data emphasize the importance of glutamylation in all types of microtubules and strengthen the hypothesis of its role in the regulation of the intracellular traffic and flagellar motility.
α和β微管蛋白亚型的谷氨酰化是一种主要的翻译后修饰,可产生主要存在于神经微管、中心粒和轴丝中的多种亚型。单谷氨酰化微管蛋白亚型可被两种单克隆抗体B3和GT335特异性识别,这两种抗体也都能识别多谷氨酰化亚型。在本研究中,使用这两种单克隆抗体进行免疫电子显微镜和免疫荧光分析,以确定在其微管蛋白亚型已明确的特定生物学模型中谷氨酰化微管蛋白亚型的表达和分布。在小鼠精子中,鞭毛的微管含有多谷氨酰化亚型,但在顶端仅检测到单谷氨酰化亚型。在精子细胞中,只有一部分袖套微管含有单谷氨酰化微管蛋白亚型。支持细胞的细胞质微管是单谷氨酰化的。生殖细胞的有丝分裂和减数分裂纺锤体是单谷氨酰化的,而HeLa细胞有丝分裂纺锤体是多谷氨酰化的。根据微管蛋白谷氨酰化的程度和范围展示了三种轴丝模型。在肺纤毛细胞中,轴丝均匀地多谷氨酰化。在海胆精子和衣藻中,鞭毛微管在近端部分多谷氨酰化,在远端部分单谷氨酰化。在草履虫中,纤毛仅在基部双谷氨酰化或单谷氨酰化。在所有细胞中,中心粒或基体都是多谷氨酰化的。这些新数据强调了谷氨酰化在所有类型微管中的重要性,并强化了其在调节细胞内运输和鞭毛运动中作用的假说。