Triviños-Lagos L, Ohmachi T, Albrightson C, Burns R G, Ennis H L, Chisholm R L
Department of Cell, Molecular and Structural Biology, Northwestern University Medical School, Chicago, IL 60611.
J Cell Sci. 1993 Aug;105 ( Pt 4):903-11. doi: 10.1242/jcs.105.4.903.
As a step in the characterization of the microtubule system of Dictyostelium discoideum, we have isolated and sequenced full-length cDNA clones that encode the Dictyostelium alpha- and beta-tubulins, as well as the Dictyostelium alpha-tubulin gene. Southern blot analysis suggests that Dictyostelium is unusual in that its genome contains single alpha- and beta-tubulin genes, rather than the multi-gene family common in most eukaryotic organisms. The complete alpha-tubulin cDNA contains 1558 nucleotides, with an open reading frame, that encode a protein of 457 amino acids. The complete beta-tubulin cDNA contains 1572 nucleotides and encodes a protein of 456 amino acids. Analysis of the deduced protein sequences indicates that while there is a significant degree of sequence similarity between the Dictyostelium tubulins and other known tubulins, the Dictyostelium alpha-tubulin displays the greatest sequence divergence yet described. Single alpha- and beta-tubulin transcripts are detected by northern blot analysis during all stages of Dictyostelium development. The highest levels of message accumulate late in germinating spores and vegetative amoebae. Despite changes in alpha- and beta-tubulin mRNA levels, protein levels remain constant throughout development. We have expressed the carboxy-terminal two-thirds of the alpha- and beta-tubulins as trpE fusions in Escherichia coli and used this protein to produce polyclonal antisera specific for the Dictyostelium alpha- and beta-tubulins. These antisera recognize one alpha- and two beta-tubulin spots on western blots of 2-D gels and, by indirect immunofluorescence, both recognize the interphase and mitotic microtubule arrays in vegetative amoebae.
作为对盘基网柄菌微管系统进行特征描述的一个步骤,我们已分离并测序了编码盘基网柄菌α-和β-微管蛋白以及α-微管蛋白基因的全长cDNA克隆。Southern印迹分析表明,盘基网柄菌不同寻常之处在于其基因组含有单个α-和β-微管蛋白基因,而非大多数真核生物中常见的多基因家族。完整的α-微管蛋白cDNA包含1558个核苷酸,有一个开放阅读框,编码一个457个氨基酸的蛋白质。完整的β-微管蛋白cDNA包含1572个核苷酸,编码一个456个氨基酸的蛋白质。对推导的蛋白质序列分析表明,虽然盘基网柄菌微管蛋白与其他已知微管蛋白之间存在显著程度的序列相似性,但盘基网柄菌α-微管蛋白显示出迄今所描述的最大序列差异。在盘基网柄菌发育的所有阶段,通过Northern印迹分析检测到单个α-和β-微管蛋白转录本。最高水平的信息在萌发孢子后期和营养性变形虫中积累。尽管α-和β-微管蛋白mRNA水平发生变化,但蛋白质水平在整个发育过程中保持恒定。我们已在大肠杆菌中表达了α-和β-微管蛋白羧基末端的三分之二作为trpE融合蛋白,并使用该蛋白产生了针对盘基网柄菌α-和β-微管蛋白的多克隆抗血清。这些抗血清在二维凝胶的western印迹上识别一个α-微管蛋白斑点和两个β-微管蛋白斑点,并且通过间接免疫荧光,两者都识别营养性变形虫中的间期和有丝分裂微管阵列。