Lechtreck K F, Geimer S
Institut Curie, UMR 144 du CNRS, Paris, France.
Cell Motil Cytoskeleton. 2000 Nov;47(3):219-35. doi: 10.1002/1097-0169(200011)47:3<219::AID-CM5>3.0.CO;2-Q.
Polyglutamylation is a widely distributed posttranslational modification of tubulin that can be demonstrated either by biochemical analysis or by the use of specific antibodies like GT335. Western blotting using GT335 demonstrated that polyglutamylated tubulin is enriched in isolated basal apparatus of Spermatozopsis similis. Single- and double-labeling experiments, using indirect immunofluorescence and immunogold electron microscopy of isolated cytoskeletons of S. similis and Chlamydomonas reinhardtii, revealed that polyglutamylated tubulin was predominately present in the basal bodies and the proximal part of the axonemes. Using immunogold labeling of whole mounts of Spermatozopsis cytoskeletons, we obtained evidence for a predominant occurrence of polyglutamylated tubulin in the B-tubule of the axonemal doublets. Polyglutamylation occurs early during premitotic basal body assembly in S. similis, whereas the probasal bodies of Chlamydomonas, which are present through interphase, showed a reduced staining with GT335 indicating that polyglutamylation is involved in basal body maturation. During flagella regeneration of C. reinhardtii, polyglutamylation preceded detyrosination and became visible shortly after the onset of flagellar regeneration. In C. reinhardtii and S. similis polyglutamylated tubulin was absent or highly reduced in the flagellar transition region, a specialized part of the flagellum linking the basal body to the axoneme. Furthermore, the transition region and the neighboring part of the axoneme showed reduced staining with L3, an antibody directed against detyrosinated tubulin. The results indicate that differences in the modification pattern can occur in a confined area of individual microtubules. The deficiency of polyglutamylated and detyrosinated tubulin in the transition region could have functional implications for flagellar turnover or excision.
多聚谷氨酰胺化是一种广泛分布的微管蛋白翻译后修饰,可通过生化分析或使用如GT335等特异性抗体来证实。使用GT335进行的蛋白质免疫印迹分析表明,多聚谷氨酰胺化的微管蛋白在分离出的相似精子藻基部装置中富集。通过对相似精子藻和莱茵衣藻分离出的细胞骨架进行间接免疫荧光和免疫金电子显微镜的单标记和双标记实验,发现多聚谷氨酰胺化的微管蛋白主要存在于基体和轴丝的近端部分。通过对精子藻细胞骨架整装标本进行免疫金标记,我们获得证据表明多聚谷氨酰胺化的微管蛋白主要存在于轴丝双联体的B微管中。多聚谷氨酰胺化在相似精子藻有丝分裂前基体组装的早期阶段发生,而莱茵衣藻在间期存在的原基体用GT335染色减弱,表明多聚谷氨酰胺化参与基体成熟。在莱茵衣藻鞭毛再生过程中,多聚谷氨酰胺化先于去酪氨酸化,并且在鞭毛再生开始后不久就可见。在莱茵衣藻和相似精子藻中,鞭毛过渡区(连接基体和轴丝的鞭毛特化部分)不存在或高度减少多聚谷氨酰胺化的微管蛋白。此外,过渡区和轴丝的相邻部分用L3(一种针对去酪氨酸化微管蛋白的抗体)染色减弱。结果表明,修饰模式的差异可能发生在单个微管的特定区域。过渡区多聚谷氨酰胺化和去酪氨酸化微管蛋白的缺乏可能对鞭毛更新或切除具有功能意义。