Department of Microbiology, Faculty of Natural Sciences and Technology VIII, Saarland University, Saarbrücken, Germany.
PLoS One. 2013 Dec 4;8(12):e82058. doi: 10.1371/journal.pone.0082058. eCollection 2013.
How misfolded proteins are exported from the ER to the cytosol for degradation (ER-associated Degradation, ERAD) and which proteins are participating in this process is not understood. Several studies using a single, leaky mutant indicated that Sec63p might be involved in ERAD. More recently, Sec63p was also found strongly associated with proteasomes attached to the protein-conducting channel in the ER membrane which presumably form part of the export machinery. These observations prompted us to reinvestigate the role of Sec63p in ERAD by generating new mutants which were selected in a screen monitoring the intracellular accumulation of the ERAD substrate CPY*. We show that a mutation in the DnaJ-domain of Sec63p causes a defect in ERAD, whereas mutations in the Brl, acidic, and transmembrane domains only affect protein import into the ER. Unexpectedly, mutations in the acidic domain which mediates interaction of Sec63p with Sec62p also caused defects in cotranslational import. In contrast to mammalian cells where SEC63 expression levels affect steady-state levels of multi-spanning transmembrane proteins, the sec63 J-domain mutant was only defective in ERAD of soluble substrates.
内质网中错误折叠的蛋白质如何被输出到细胞质中进行降解(内质网相关降解,ERAD),以及哪些蛋白质参与了这个过程,目前还不清楚。一些使用单个渗漏突变体的研究表明 Sec63p 可能参与 ERAD。最近,Sec63p 也被发现与附着在 ER 膜中蛋白质传导通道上的蛋白酶体强烈相关,这些蛋白酶体可能构成了出口机制的一部分。这些观察结果促使我们通过生成新的突变体来重新研究 Sec63p 在 ERAD 中的作用,这些突变体是在监测 ERAD 底物 CPY*在细胞内积累的筛选中选择出来的。我们表明,Sec63p 的 DnaJ 结构域中的突变导致 ERAD 缺陷,而 Brl、酸性和跨膜结构域中的突变仅影响蛋白质向 ER 的输入。出乎意料的是,介导 Sec63p 与 Sec62p 相互作用的酸性结构域中的突变也导致共翻译输入缺陷。与哺乳动物细胞中 SEC63 表达水平影响多跨膜蛋白的稳态水平不同,sec63 J 结构域突变体仅在可溶性底物的 ERAD 中缺陷。