Nakajima H, Hirata A, Ogawa Y, Yonehara T, Yoda K, Yamasaki M
Department of Agricultural Chemistry, University of Tokyo, Japan.
J Cell Biol. 1991 Apr;113(2):245-60. doi: 10.1083/jcb.113.2.245.
The Saccharomyces cerevisiae mutant strains blocked in the protein secretion pathway are not able to induce sexual aggregation. We have utilized the defect of aggregation to concentrate the secretion-deficient cells and identified a new gene which functions in the process of intracellular protein transport. The new mutant, uso1, is temperature sensitive for growth and protein secretion. At the restrictive temperature (37 degrees C), uso1 mutant accumulated the core-glycosylated precursor form of the exported protein invertase in the cells. Ultrastructural study of the mutant fixed by the freeze-substitution method revealed expansion of the nuclear envelope lumen and accumulation of the ER at the restrictive temperature. Abnormally oriented bundles of microtubules were often found in the nucleus. The USO1 gene was cloned by complementation of the uso1 temperature-sensitive growth defect. DNA sequence analysis revealed a hydrophilic protein of 1790 amino acids with a COOH-terminal 1,100-amino acid-long alpha-helical structure characteristic of the coiled-coil rod region of the cytoskeleton-related proteins. These observations suggest that Uso1 protein plays a role as a cytoskeletal component in the protein transport from the ER to the later secretory compartments.
在蛋白质分泌途径中受阻的酿酒酵母突变菌株无法诱导有性聚集。我们利用聚集缺陷来浓缩分泌缺陷细胞,并鉴定出一个在细胞内蛋白质运输过程中起作用的新基因。新的突变体uso1对生长和蛋白质分泌具有温度敏感性。在限制温度(37摄氏度)下,uso1突变体在细胞内积累了分泌型蛋白蔗糖酶的核心糖基化前体形式。通过冷冻替代法固定的突变体的超微结构研究显示,在限制温度下核膜腔扩张且内质网积累。在细胞核中经常发现微管束方向异常。通过互补uso1温度敏感生长缺陷克隆了USO1基因。DNA序列分析揭示了一种由1790个氨基酸组成的亲水性蛋白质,其COOH末端具有1100个氨基酸长的α螺旋结构,这是细胞骨架相关蛋白的卷曲螺旋杆区域的特征。这些观察结果表明,Uso1蛋白在从内质网到后期分泌区室的蛋白质运输中作为细胞骨架成分发挥作用。