Loh Eva, Peter Frank, Subramaniam V Nathan, Hong Wanjin
Membrane Biology Laboratory, Institute of Molecular and Cell Biology, 61 Biopolis Drive, Singapore 138673, Republic of Singapore.
J Cell Sci. 2005 Mar 15;118(Pt 6):1209-22. doi: 10.1242/jcs.01723. Epub 2005 Feb 22.
The TRAPP complex identified in yeast regulates vesicular transport in the early secretory pathway. Although some components of the TRAPP complex are structurally conserved in mammalian cells, the function of the mammalian components has not been examined. We describe our biochemical and functional analysis of mammalian Bet3, the most conserved component of the TRAPP complex. Bet3 mRNA is ubiquitously expressed in all tissues. Antibodies raised against recombinant Bet3 specifically recognize a protein of 22 kDa. In contrast to yeast Bet3p, the majority of Bet3 is present in the cytosol. To investigate the possible involvement of Bet3 in transport events in mammalian cells, we utilized a semi-intact cell system that reconstitutes the transport of the envelope glycoprotein of vesicular stomatitis virus (VSV-G) from the ER to the Golgi apparatus. In this system, antibodies against Bet3 inhibit transport in a dose-dependent manner, and cytosol that is immunodepleted of Bet3 is also defective in this transport. This defect can be rescued by supplementing the Bet3-depleted cytosol with recombinant GST-Bet3. We also show that Bet3 acts after COPII but before Rab1, alpha-SNAP and the EGTA-sensitive stage during ER-Golgi transport. Gel filtration analysis demonstrates that Bet3 exists in two distinct pools in the cytosol, the high-molecular-weight pool may represent the TRAPP complex, whereas the other probably represents the monomeric Bet3.
在酵母中鉴定出的TRAPP复合物调节早期分泌途径中的囊泡运输。尽管TRAPP复合物的一些组分在哺乳动物细胞中结构保守,但哺乳动物组分的功能尚未得到研究。我们描述了对哺乳动物Bet3(TRAPP复合物中最保守的组分)的生化和功能分析。Bet3 mRNA在所有组织中普遍表达。针对重组Bet3产生的抗体特异性识别一种22 kDa的蛋白质。与酵母Bet3p不同,大部分Bet3存在于细胞质中。为了研究Bet3在哺乳动物细胞运输事件中的可能作用,我们利用了一种半完整细胞系统,该系统重建了水泡性口炎病毒(VSV-G)包膜糖蛋白从内质网到高尔基体的运输。在这个系统中,抗Bet3抗体以剂量依赖性方式抑制运输,并且免疫耗尽Bet3的细胞质在这种运输中也有缺陷。通过用重组GST-Bet3补充耗尽Bet3的细胞质可以挽救这种缺陷。我们还表明,Bet3在内质网-高尔基体运输过程中在COPII之后但在Rab1、α-SNAP和EGTA敏感阶段之前起作用。凝胶过滤分析表明,Bet3在细胞质中以两个不同的池存在,高分子量池可能代表TRAPP复合物,而另一个可能代表单体Bet3。