Aström H
Department of Botany, University of Helsinki, Finland.
Cell Biol Int Rep. 1992 Sep;16(9):871-81.
Three monoclonal alpha-tubulin antibodies YL 1/2 (Kilmartin et al., 1982), 6-11B-1 (Piperno and Fuller, 1985) and DM1A (Blose et al., 1984) were used in indirect immunofluorescence (IIF) microscopy of the microtubule (MT) cytoskeleton in tobacco (Nicotiana tabacum) pollen tubes. The majority of pollen tube MTs contain tyrosinated alpha-tubulin recognized by YL 1/2. Acetylated alpha-tubulin revealed by 6-11B-1 was detected in the generative cell and in the kinetochore fibers, in polar spindle regions, and in the cell plate of the phragmoplast during generative cell division. In addition, small fragments of acetylated microtubules were seen in the older parts of the pollen tube grown on a taxol medium. The interaction of pollen tube MTs with mAb 6-11B-1 suggested that acetylation of alpha-tubulin correlates well with the putative arrays of stable MTs.
三种抗α-微管蛋白单克隆抗体YL 1/2(Kilmartin等人,1982年)、6-11B-1(Piperno和Fuller,1985年)以及DM1A(Blose等人,1984年)被用于烟草(Nicotiana tabacum)花粉管微管(MT)细胞骨架的间接免疫荧光(IIF)显微镜观察。大多数花粉管微管含有可被YL 1/2识别的酪氨酸化α-微管蛋白。6-11B-1所显示的乙酰化α-微管蛋白在生殖细胞、动粒纤维、极性纺锤体区域以及生殖细胞分裂期间成膜体的细胞板中被检测到。此外,在紫杉醇培养基上生长的花粉管较老部分可见乙酰化微管的小片段。花粉管微管与单克隆抗体6-11B-1的相互作用表明,α-微管蛋白的乙酰化与假定的稳定微管阵列密切相关。