Vo Diep-Khanh, Engler Alexander, Stoimenovski Darko, Hartig Roland, Kaehne Thilo, Kalinski Thomas, Naumann Michael, Haybaeck Johannes, Nass Norbert
Department of Pathology, Medical Faculty, Otto-von-Guericke University Magdeburg, D-39120 Magdeburg, Germany.
Institute of Experimental Internal Medicine, Medical Faculty, Otto von Guericke University, D-39120 Magdeburg, Germany.
Cancers (Basel). 2021 Mar 14;13(6):1293. doi: 10.3390/cancers13061293.
Translation initiation comprises complex interactions of eukaryotic initiation factor (eIF) subunits and the structural elements of the mRNAs. Translation initiation is a key process for building the cell's proteome. It not only determines the total amount of protein synthesized but also controls the translation efficiency for individual transcripts, which is important for cancer or ageing. Thus, understanding protein interactions during translation initiation is one key that contributes to understanding how the eIF subunit composition influences translation or other pathways not yet attributed to eIFs. We applied the BioID technique to two rapidly dividing cell lines (the immortalized embryonic cell line HEK-293T and the colon carcinoma cell line HCT-166) in order to identify interacting proteins of eIF3A, a core subunit of the eukaryotic initiation factor 3 complex. We identified a total of 84 interacting proteins, with very few proteins being specific to one cell line. When protein biosynthesis was blocked by thapsigargin-induced endoplasmic reticulum (ER) stress, the interacting proteins were considerably smaller in number. In terms of gene ontology, although eIF3A interactors are mainly part of the translation machinery, protein folding and RNA binding were also found. Cells suffering from ER-stress show a few remaining interactors which are mainly ribosomal proteins or involved in RNA-binding.
翻译起始包括真核生物起始因子(eIF)亚基与mRNA结构元件之间的复杂相互作用。翻译起始是构建细胞蛋白质组的关键过程。它不仅决定了合成蛋白质的总量,还控制着单个转录本的翻译效率,这对癌症或衰老很重要。因此,了解翻译起始过程中的蛋白质相互作用是有助于理解eIF亚基组成如何影响翻译或其他尚未归因于eIFs的途径的关键之一。我们将生物识别技术应用于两种快速分裂的细胞系(永生化胚胎细胞系HEK-293T和结肠癌细胞系HCT-166),以鉴定真核生物起始因子3复合物的核心亚基eIF3A的相互作用蛋白。我们总共鉴定出84种相互作用蛋白,很少有蛋白是某一种细胞系特有的。当毒胡萝卜素诱导的内质网(ER)应激阻断蛋白质生物合成时,相互作用蛋白的数量大幅减少。在基因本体论方面,虽然eIF3A相互作用蛋白主要是翻译机制的一部分,但也发现了蛋白质折叠和RNA结合相关蛋白。内质网应激细胞中显示出一些剩余的相互作用蛋白,它们主要是核糖体蛋白或参与RNA结合。