That T C, Rossier C, Barja F, Turian G, Roos U P
Laboratory of General Microbiology, University of Geneva, Switzerland.
Eur J Cell Biol. 1988 Apr;46(1):68-79.
The antitubulin fungicide benomyl suppressed the linear growth of Neurospora crassa wild type strain St. Lawrence 74 at micromolar concentrations. The rate of germination of macroconidia was not affected. Macroconidia exposed to 1.7 microM benomyl for 5 h formed multiple germ tubes. When germlings incubated for 4 h were exposed to 1.7 microM benomyl for 3 h, their germ tube stopped growing, swelled and emitted several branches. Normal linear growth was restored after removal of the fungicide. Linear growth of N. crassa was resistant up to 16 microM nocodazole. This drug induced multipolar germination at 8 microM, and griseofulvin only at 140 microM. The microtubule (MT) cytoskeleton of N. crassa could be revealed by indirect immunofluorescence with the monoclonal antibody YOL 1/34 directed against yeast alpha-tubulin. We detected no striking effects of the benomyl treatments on MT organization. The MT-stabilizing agents deuterium oxide (D2O) and cAMP have no antagonistic effects on the benomyl-induced multipolar germination. The positioning of nuclei and mitochondria was determined from the DAPI and Rhodamine 123 fluorescence patterns, respectively. Benomyl inhibited nuclear migration into multiple germ tubes. Quantitative scanning cytophotometry revealed a peak in the intensity of the mitochondria-associated Rhodamine 123 fluorescence near the apex of untreated germlings. This peak disappeared in multiple germ tubes. Benomyl-resistant mutant bml 511 (r), mutated in its beta-tubulin gene, germinated normally in the presence of the fungicide. This strongly suggests that multiple germ tube formation was due to the effect of benomyl on beta-tubulin. Benomyl-resistant strain 74-3, constructed by reintroducing the cloned mutant N. crassa beta-tubulin gene into the cells by transformation, displayed a partial resistance to benomyl with respect to multipolar germination. Its rate of germination was slow (50% germination reached after 4 h at 37 degrees C as compared to 2.5 h for the wild type). In contrast to N. crassa, the other ascomycete Aspergillus nidulans is nocodazole-sensitive (linear growth suppressed at 1.6 microM). It did not respond to the MT inhibitors benomyl and nocodazole with respect to the pattern of germ tube emergence. Our results suggest that microtubule or membrane beta-tubulin is involved in the maintenance of developmental polarity during germ tube emergence and growth of N. crassa.
抗微管蛋白杀菌剂苯菌灵在微摩尔浓度下可抑制粗糙脉孢菌野生型菌株圣劳伦斯74的线性生长。大分生孢子的萌发率不受影响。暴露于1.7微摩尔苯菌灵5小时的大分生孢子形成了多个芽管。将培养4小时的菌丝体暴露于1.7微摩尔苯菌灵3小时后,其芽管停止生长、肿胀并发出多个分支。去除杀菌剂后恢复了正常的线性生长。粗糙脉孢菌的线性生长对高达16微摩尔的诺考达唑具有抗性。该药物在8微摩尔时诱导多极萌发,而灰黄霉素仅在140微摩尔时诱导多极萌发。粗糙脉孢菌的微管(MT)细胞骨架可用针对酵母α-微管蛋白的单克隆抗体YOL 1/34通过间接免疫荧光法显示。我们未检测到苯菌灵处理对MT组织有显著影响。MT稳定剂氧化氘(D2O)和环磷酸腺苷(cAMP)对苯菌灵诱导的多极萌发没有拮抗作用。分别根据4,6-二脒基-2-苯基吲哚(DAPI)和罗丹明123的荧光模式确定细胞核和线粒体的定位。苯菌灵抑制细胞核向多个芽管的迁移。定量扫描细胞光度法显示,在未处理的菌丝体顶端附近,与线粒体相关的罗丹明123荧光强度有一个峰值。这个峰值在多个芽管中消失。对苯菌灵具有抗性的突变体bml 511(r),其β-微管蛋白基因发生了突变,但在杀菌剂存在的情况下仍能正常萌发。这有力地表明,多个芽管的形成是由于苯菌灵对β-微管蛋白的作用。通过转化将克隆的粗糙脉孢菌突变体β-微管蛋白基因重新导入细胞构建的对苯菌灵具有抗性的菌株74-3,在多极萌发方面对苯菌灵表现出部分抗性。其萌发率较慢(在37℃下4小时后达到50%萌发,而野生型为2.5小时)。与粗糙脉孢菌不同,另一种子囊菌烟曲霉对诺考达唑敏感(在1.6微摩尔时线性生长受到抑制)。就芽管出现模式而言,它对MT抑制剂苯菌灵和诺考达唑没有反应。我们的结果表明,微管或膜β-微管蛋白参与了粗糙脉孢菌芽管出现和生长过程中发育极性 的维持。