De Marco N, Tussellino M, Carotenuto R, Ronca R, Rizzolio S, Biffo S, Campanella C
Department of Biology, University of Naples Federico II , Monte Sant'Angelo, via Cinthia, Naples, Italy.
Candiolo Cancer Institute IRCSS, Turin, Italy.
Dev Biol. 2017 Jul 1;427(1):148-154. doi: 10.1016/j.ydbio.2017.04.017. Epub 2017 May 1.
The eukaryotic initiation translation factor eIF6 is a highly conserved, essential protein implicated in translation. eIF6 is regulated in vivo by extracellular signals, such as IGF signaling (for a review see Miluzio et al., 2009). In Xenopus, eif6 over-expression causes a delay in eye development (De Marco et al., 2011). In this study we showed that eif6 co-immunoprecipitates with the insulin-like growth factor receptor (igfr) and may function downstream of igf in eye formation. The relationship between eif6 and gipc2, a protein partner of a variety of molecules including membrane proteins, was investigated. gipc2 is required for maintaining igf-induced akt activation on eye development (Wu et al., 2006). Significantly eif6 and gipc2 have opposite effects in eye development. While eif6 is required for eye formation below threshold levels, gipc2 knockdown impairs eye development (De Marco et al., 2011; Wu et al., 2006). In this study, it was shown that in eif6 over-expressors, the delay in eye morphogenesis is reversed by gipc2 injection, while the injection of eif6 down-regulates gipc2 expression. Real-time-PCR indicates that eif6 regulates gipc2 expression in a dose-dependent manner. In contrast, gipc2 knockdown has no significant effect on eif6 mRNA levels. These results suggest that eif6 regulation of gipc2 enables correct morphogenesis of Xenopus eye and stimulate questions on the molecular network implicated in this process.
真核生物起始翻译因子eIF6是一种高度保守的必需蛋白,与翻译过程有关。eIF6在体内受细胞外信号调节,如胰岛素样生长因子信号(综述见Miluzio等人,2009年)。在非洲爪蟾中,eif6过表达会导致眼睛发育延迟(De Marco等人,2011年)。在本研究中,我们发现eif6与胰岛素样生长因子受体(igfr)共免疫沉淀,可能在眼睛形成过程中发挥igf下游的作用。我们研究了eif6与gipc2之间的关系,gipc2是包括膜蛋白在内的多种分子的蛋白伴侣。gipc2是维持igf诱导的眼睛发育中akt激活所必需的(Wu等人,2006年)。值得注意的是,eif6和gipc2在眼睛发育中具有相反的作用。虽然低于阈值水平时眼睛形成需要eif6,但敲低gipc2会损害眼睛发育(De Marco等人,2011年;Wu等人,2006年)。在本研究中,结果表明在eif6过表达的动物中,注射gipc2可逆转眼睛形态发生的延迟,而注射eif6会下调gipc2的表达。实时定量PCR表明eif6以剂量依赖的方式调节gipc2的表达。相反,敲低gipc2对eif6 mRNA水平没有显著影响。这些结果表明,eif6对gipc2的调节使非洲爪蟾眼睛能够正确形态发生,并引发了对这一过程中涉及的分子网络的质疑。