Solnica-Krezel L, Dove W F, Burland T G
McArdle Laboratory for Cancer Research, University of Wisconsin, Madison 53706.
J Gen Microbiol. 1988 May;134(5):1323-31. doi: 10.1099/00221287-134-5-1323.
Uninucleate amoebae of Physarum polycephalum strain CL undergo apogamic development to form multinucleate plasmodia via an intermediate stage of large, uninucleate cells irreversibly committed to plasmodial development. This amoebal-plasmodial transition involves major changes in tubulin gene expression and the organization of microtubular structures. We analysed the expression of the betC locus, which encodes the plasmodial-specific beta 2-tubulin, during plasmodial development. A key question addressed was the timing of expression of betC in relation to the last open mitosis of the amoeba and the first closed mitosis of the plasmodium during the transition. Culture conditions were improved to yield partly synchronous differentiating cultures containing 50-60% committed cells, in order to facilitate biochemical analysis of development. Northern blotting indicated that betC RNA was virtually absent from amoebae and from early differentiating cultures. However, betC transcripts could already be detected in differentiating cultures containing only 0.1% of committed cells; the relative amount of betC transcripts increased as the percentage of committed cells in differentiating cultures increased. In fully developed plasmodia, there was at least a 330-fold increase in the betC transcript level compared to that in amoebae. We conclude that betC is activated during the amoebal-plasmodial transition immediately before or during the commitment event. Small amounts of beta 2-tubulin polypeptide could first be detected by Western blotting around the stage of the first closed mitosis. Thus beta 2-tubulin may participate in the first closed mitosis that committed cells undergo during their development into plasmodia.
多头绒泡菌CL菌株的单核变形虫通过一个不可逆地进入原质团发育的大型单核细胞中间阶段进行无融合生殖发育,形成多核原质团。这种变形虫 - 原质团转变涉及微管蛋白基因表达和微管结构组织的重大变化。我们分析了在原质团发育过程中编码原质团特异性β2 - 微管蛋白的betC基因座的表达。一个关键问题是betC在转变过程中相对于变形虫的最后一次开放有丝分裂和原质团的第一次封闭有丝分裂的表达时间。改善了培养条件以产生部分同步分化的培养物,其中含有50 - 60%的定向细胞,以便于对发育进行生化分析。Northern印迹表明,betC RNA在变形虫和早期分化培养物中几乎不存在。然而,在仅含有0.1%定向细胞的分化培养物中已经可以检测到betC转录本;随着分化培养物中定向细胞百分比的增加,betC转录本的相对量增加。在完全发育的原质团中,与变形虫相比,betC转录本水平至少增加了330倍。我们得出结论,betC在变形虫 - 原质团转变过程中紧接在定向事件之前或期间被激活。通过蛋白质印迹法在第一次封闭有丝分裂阶段左右首次可以检测到少量的β2 - 微管蛋白多肽。因此,β2 - 微管蛋白可能参与定向细胞在发育成原质团过程中经历的第一次封闭有丝分裂。