Acetylated alpha-tubulin in the pollen tube microtubules.

Cell biology international reports Pub Date : 1992-09-01
H Aström
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引用次数: 0

Abstract

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.

花粉管微管中的乙酰化α-微管蛋白
三种单克隆α-微管蛋白抗体 YL 1/2(Kilmartin 等人,1982 年)、6-11B-1(Piperno 和 Fuller,1985 年)和 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)显微镜检查。大多数花粉管 MT 含有被 YL 1/2 识别的酪氨酸化α-微管蛋白。生成细胞分裂过程中,在生成细胞、动心轴纤维、极性纺锤体区域和膈细胞的细胞板中检测到由 6-11B-1 揭示的乙酰化α-微管蛋白。此外,在紫杉醇培养基上生长的花粉管较老部分也能看到乙酰化微管的小碎片。花粉管 MT 与 mAb 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 MT 阵列密切相关。
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