Toikkanen J, Gatti E, Takei K, Saloheimo M, Olkkonen V M, Söderlund H, De Camilli P, Keränen S
VTT, Biotechnology and Food Research, Finland.
Yeast. 1996 Apr;12(5):425-38. doi: 10.1002/(SICI)1097-0061(199604)12:5%3C425::AID-YEA924%3E3.0.CO;2-B.
A yeast gene (cDNA clone) was isolated in a screen for suppressors of secretion-defective sec15-1 mutation. This gene encodes a protein homologous to the beta subunit of the mammalian Sec61 protein complex functioning in protein translocation into the endoplasmic reticulum (ER). The predicted protein, Seb1p, consists of 82 amino acids and contains one potential membrane-spanning region at the C-terminus but no N-terminal signal sequence. Seb1p shows 30% identity to the mammalian Sec61 beta subunit and 34% identity to the Arabidopsis thaliana Sec61 beta subunit. Overexpression of SEB1 from a multicopy plasmid suppressed the temperature sensitivity of sec61-2 and sec61-3 mutants. Immunofluorescence and immunoelectron microscopy indicated that Seb1p resides in the ER membranes with the hydrophilic N-terminus exposed to the cytoplasm. The in vitro translated Seb1p was post-translationally inserted into microsomal membranes. As the chromosomal disruption of the SEB1 gene was not lethal, potential homologous genes were screened by heterologous hybridization. The SEB1 homologue thus isolated, SEB2, encodes a protein 53% identical to Seb1p. Disruption of the chromosomal SEB2 was not lethal whereas the double disruption of SEB1 and SEB2 resulted in a temperature-sensitive phenotype. This study further emphasizes the evolutionary conservation of the ER protein translocation apparatus and provides novel genetic tools for its functional analysis.
在对分泌缺陷型sec15 - 1突变的抑制子进行筛选时,分离出了一个酵母基因(cDNA克隆)。该基因编码一种与哺乳动物Sec61蛋白复合体的β亚基同源的蛋白质,Sec61蛋白复合体在蛋白质转运到内质网(ER)中发挥作用。预测的蛋白质Seb1p由82个氨基酸组成,在C末端含有一个潜在的跨膜区域,但没有N末端信号序列。Seb1p与哺乳动物Sec61β亚基的同一性为30%,与拟南芥Sec61β亚基的同一性为34%。从多拷贝质粒中过表达SEB1可抑制sec61 - 2和sec61 - 3突变体的温度敏感性。免疫荧光和免疫电子显微镜表明,Seb1p定位于内质网膜,其亲水性N末端暴露于细胞质中。体外翻译的Seb1p在翻译后插入微粒体膜中。由于SEB1基因的染色体破坏并不致命,因此通过异源杂交筛选潜在的同源基因。由此分离出的SEB1同源物SEB2编码一种与Seb1p同一性为53%的蛋白质。染色体SEB2的破坏并不致命,而SEB1和SEB2的双重破坏导致温度敏感表型。这项研究进一步强调了内质网蛋白质转运装置的进化保守性,并为其功能分析提供了新的遗传工具。