Burland T G, Gull K, Schedl T, Boston R S, Dove W F
J Cell Biol. 1983 Dec;97(6):1852-9. doi: 10.1083/jcb.97.6.1852.
Three alpha-tubulins and two beta-tubulins have been resolved by two-dimensional gel electrophoresis of whole cell lysates of Physarum myxamoebae or plasmodia. Criteria used to identify the tubulins included migration on two-dimensional gels with myxamoebal tubulins purified by self-assembly into microtubules in vitro, peptide mapping with Staphylococcus V8 protease and with chymotrypsin, immunoprecipitation with a monoclonal antibody specific for beta-tubulin, and, finally, hybrid selection of specific mRNA by cloned tubulin DNA sequences, followed by translation in vitro. Differential expression of the Physarum tubulins was observed. The alpha 1- and beta 1-tubulins were detected in both myxamoebae and plasmodia; alpha 2 and beta 2 were detected only in plasmodia, alpha 3 was detected only in the myxamoebal phase, and may be specific to the flagellate. Observation of more tubulin species in plasmodia than in myxamoebae was remarkable; the only microtubules detected in plasmodia are those of the mitotoic spindle, whereas myxamoebae display cytoplasmic, centriolar, flagellar, and mitotic-spindle microtubules. In vitro translation of myxamoebal and plasmodial RNAs indicated that there are distinct mRNAs, and therefore probably separate genes, for the alpha 1-, alpha 2-, beta 1-, and beta 2-tubulins. Thus, the different patterns of tubulin expression in myxamoebae and plasmodia reflect differential expression of tubulin genes.
通过对多头绒泡菌变形体或原质团的全细胞裂解物进行二维凝胶电泳,已分辨出三种α - 微管蛋白和两种β - 微管蛋白。用于鉴定微管蛋白的标准包括:在二维凝胶上的迁移情况(与通过体外自组装成微管纯化的变形体微管蛋白对比)、用葡萄球菌V8蛋白酶和胰凝乳蛋白酶进行肽图谱分析、用针对β - 微管蛋白的单克隆抗体进行免疫沉淀,最后是通过克隆的微管蛋白DNA序列对特定mRNA进行杂交选择,随后进行体外翻译。观察到多头绒泡菌微管蛋白存在差异表达。α1 - 和β1 - 微管蛋白在变形体和原质团中均被检测到;α2和β2仅在原质团中被检测到,α3仅在变形体阶段被检测到,且可能是鞭毛虫特有的。原质团中检测到的微管蛋白种类比变形体中的更多,这一现象值得注意;原质团中检测到的唯一微管是有丝分裂纺锤体微管,而变形体则显示出细胞质、中心粒、鞭毛和有丝分裂纺锤体微管。对变形体和原质团RNA的体外翻译表明,α1 - 、α2 - 、β1 - 和β2 - 微管蛋白有不同的mRNA,因此可能有不同的基因。所以,变形体和原质团中微管蛋白表达的不同模式反映了微管蛋白基因的差异表达。