Asano K, Kinzy T G, Merrick W C, Hershey J W
Department of Biological Chemistry, School of Medicine, University of California, Davis 95616, USA.
J Biol Chem. 1997 Jan 10;272(2):1101-9. doi: 10.1074/jbc.272.2.1101.
The largest of the mammalian translation initiation factors, eIF3, consists of at least eight subunits ranging in mass from 35 to 170 kDa. eIF3 binds to the 40 S ribosome in an early step of translation initiation and promotes the binding of methionyl-tRNAi and mRNA. We report the cloning and characterization of human cDNAs encoding two of its subunits, p110 and p36. It was found that the second slowest band during polyacrylamide gel electrophresis of eIF3 subunits in sodium dodecyl sulfate contains two proteins: p110 and p116. Analysis of the cloned cDNA encoding p110 indicates that its amino acid sequence is 31% identical to that of the yeast protein, Nip1. The p116 cDNA was cloned and characterized as a human homolog of yeast Prt1, as described elsewhere (Methot, N., Rom, E., Olsen, H., and Sonenberg, N. (1997) J. Biol. Chem. 272, 1110-1116). p36 is a WD40 repeat protein, which is 46% identical to the p39 subunit of yeast eIF3 and is identical to TRIP-1, a phosphorylation substrate of the TGF-beta type II receptor. The p116, p110, and p36 subunits localize on 40 S ribosomes in cells active in translation and co-immunoprecipitate with affinity-purified antibodies against the p170 subunit, showing that these proteins are integral components of eIF3. Although p36 and p116 have homologous protein subunits in yeast eIF3, the p110 homolog, Nip1, is not detected in yeast eIF3 preparations. The results indicate both conservation and diversity in eIF3 between yeast and humans.
哺乳动物翻译起始因子中最大的eIF3由至少八个亚基组成,其分子量在35至170 kDa之间。在翻译起始的早期步骤中,eIF3与40 S核糖体结合,并促进甲硫氨酰 - tRNAi和mRNA的结合。我们报道了编码其两个亚基p110和p36的人类cDNA的克隆和表征。发现在十二烷基硫酸钠存在下eIF3亚基的聚丙烯酰胺凝胶电泳中第二慢的条带包含两种蛋白质:p110和p116。对编码p110的克隆cDNA的分析表明,其氨基酸序列与酵母蛋白Nip1的氨基酸序列有31%的同一性。如其他地方所述(Methot, N., Rom, E., Olsen, H., and Sonenberg, N. (1997) J. Biol. Chem. 272, 1110 - 1116),p116 cDNA被克隆并表征为酵母Prt1的人类同源物。p36是一种WD40重复蛋白,与酵母eIF3的p39亚基有46%的同一性,并且与TGF-β II型受体的磷酸化底物TRIP-1相同。p116、p110和p36亚基定位于活跃进行翻译的细胞中的40 S核糖体上,并与针对p170亚基的亲和纯化抗体共免疫沉淀,表明这些蛋白质是eIF3的组成成分。尽管p36和p116在酵母eIF3中有同源蛋白亚基,但在酵母eIF3制剂中未检测到p110同源物Nip1。结果表明酵母和人类的eIF3之间既有保守性又有多样性。