Fouquet J P, Edde B, Kann M L, Wolff A, Desbruyeres E, Denoulet P
Biologie Cellulaire, Groupe Formation et Maturation du Gamète Mâle, Université Paris, France.
Cell Motil Cytoskeleton. 1994;27(1):49-58. doi: 10.1002/cm.970270106.
The distribution of glutamylated tubulin has been analyzed in mammalian testis using the specific mAb GT335 by immunoelectron microscopy and immunoblotting. In spermatozoa of various species, immunogold labeling showed the presence of glutamylated tubulin in all of the microtubules of axoneme and centrioles, whereas the microtubule network of the spermatid manchette was unlabeled. In earlier germ cells, centriole was the only microtubule structure to be labeled. A similar distribution was observed using the anti-acetylated tubulin antibody (6-11B-1), confirming previous results of Hermo et al. [Anat. Rec. 229:31-50, 1991]. However, among testicular somatic cells, microtubules of some Sertoli cell branches were not acetylated but glutamylated. 2-D PAGE of mouse and hamster sperm extracts showed a high level of alpha and beta-tubulin heterogeneity, comparable to that found in brain. Immunoblotting with GT335 revealed a large amount of glutamylated tubulin resolved into numerous alpha as well as beta-tubulin isoforms. This suggests that the major testis-specific tubulin isotypes (m alpha 3/7 and m beta 3) are also glutamylatable. These results show a subcellular sorting of posttranslationally modified tubulin isoforms in spermatids, glutamylation being associated with the most stable microtubule structures.
利用特异性单克隆抗体GT335,通过免疫电子显微镜和免疫印迹技术,对哺乳动物睾丸中谷氨酰胺化微管蛋白的分布进行了分析。在各种物种的精子中,免疫金标记显示轴丝和中心粒的所有微管中均存在谷氨酰胺化微管蛋白,而精子细胞环的微管网络未被标记。在早期生殖细胞中,中心粒是唯一被标记的微管结构。使用抗乙酰化微管蛋白抗体(6-11B-1)观察到类似的分布,证实了Hermo等人先前的结果[《解剖学记录》229:31-50,1991]。然而,在睾丸体细胞中,一些支持细胞分支的微管未被乙酰化而是被谷氨酰胺化。对小鼠和仓鼠精子提取物进行的二维聚丙烯酰胺凝胶电泳显示,α和β微管蛋白具有高度异质性,与在大脑中发现的情况相当。用GT335进行免疫印迹显示,大量谷氨酰胺化微管蛋白可分解为众多α和β微管蛋白亚型。这表明主要的睾丸特异性微管蛋白同型(mα3/7和mβ3)也可被谷氨酰胺化。这些结果显示了精子细胞中翻译后修饰的微管蛋白同型的亚细胞分选,谷氨酰胺化与最稳定的微管结构相关。