Burland T G, Paul E C, Oetliker M, Dove W F
McArdle Laboratory for Cancer Research, University of Wisconsin, Madison 53706.
Mol Cell Biol. 1988 Mar;8(3):1275-81. doi: 10.1128/mcb.8.3.1275-1281.1988.
The multinucleate plasmodium of Physarum polycephalum is unusual among eucaryotic cells in that it uses tubulins only in mitotic-spindle microtubules; cytoskeletal, flagellar, and centriolar microtubules are absent in this cell type. We have identified a beta-tubulin cDNA clone, beta 105, which is shown to correspond to the transcript of the betC beta-tubulin locus and to encode beta 2 tubulin, the beta tubulin expressed specifically in the plasmodium and used exclusively in the mitotic spindle. Physarum amoebae utilize tubulins in the cytoskeleton, centrioles, and flagella, in addition to the mitotic spindle. Sequence analysis shows that beta 2 tubulin is only 83% identical to the two beta tubulins expressed in amoebae. This compares with 70 to 83% identity between Physarum beta 2 tubulin and the beta tubulins of yeasts, fungi, alga, trypanosome, fruit fly, chicken, and mouse. On the other hand, Physarum beta 2 tubulin is no more similar to, for example, Aspergillus beta tubulins than it is to those of Drosophila melanogaster or mammals. Several eucaryotes express at least one widely diverged beta tubulin as well as one or more beta tubulins that conform more closely to a consensus beta-tubulin sequence. We suggest that beta-tubulins diverge more when their expression pattern is restricted, especially when this restriction results in their use in fewer functions. This divergence among beta tubulins could have resulted through neutral drift. For example, exclusive use of Physarum beta 2 tubulin in the spindle may have allowed more amino acid substitutions than would be functionally tolerable in the beta tubulins that are utilized in multiple microtubular organelles. Alternatively, restricted use of beta tubulins may allow positive selection to operate more freely to refine beta-tubulin function.
多头绒泡菌的多核原生质团在真核细胞中很不寻常,因为它仅在有丝分裂纺锤体微管中使用微管蛋白;这种细胞类型中不存在细胞骨架、鞭毛和中心粒微管。我们鉴定出一个β-微管蛋白cDNA克隆β105,它对应于betCβ-微管蛋白基因座的转录本,并编码β2微管蛋白,β2微管蛋白是在原生质团中特异性表达且仅用于有丝分裂纺锤体的β-微管蛋白。多头绒泡菌变形虫除了在有丝分裂纺锤体中使用微管蛋白外,还在细胞骨架、中心粒和鞭毛中使用微管蛋白。序列分析表明,β2微管蛋白与变形虫中表达的两种β-微管蛋白的同一性仅为83%。相比之下,多头绒泡菌β2微管蛋白与酵母、真菌、藻类、锥虫、果蝇、鸡和小鼠的β-微管蛋白的同一性为70%至83%。另一方面,多头绒泡菌β2微管蛋白与例如曲霉β-微管蛋白的相似性并不比与黑腹果蝇或哺乳动物的β-微管蛋白的相似性更高。几种真核生物表达至少一种差异较大的β-微管蛋白以及一种或多种更符合β-微管蛋白共有序列的β-微管蛋白。我们认为,当β-微管蛋白的表达模式受到限制时,尤其是当这种限制导致其功能使用减少时,它们的差异会更大。β-微管蛋白之间的这种差异可能是通过中性漂变产生的。例如,在纺锤体中仅使用多头绒泡菌β2微管蛋白可能允许比在多种微管细胞器中使用的β-微管蛋白在功能上可容忍的更多氨基酸替代。或者,β-微管蛋白的有限使用可能使正选择更自由地发挥作用以优化β-微管蛋白的功能。