Deramaudt T B, Remy P, Stiegler P
FRE 2168 du CNRS, Mécanismes Moléculaires de la Division Cellulaire et du Développement, Institut de Physiologie et de Chimie Biologique, 21 rue René Descartes, 67084 Strasbourg Cedex, France.
Gene. 2001 Aug 22;274(1-2):169-77. doi: 10.1016/s0378-1119(01)00610-2.
Fli and erg are two members of the ETS gene family that encodes transcription factors related to the c-ets-1 proto-oncogene. The products of the ETS genes act as transcriptional effectors in cell proliferation, differentiation, and oncogenic transformation. FLI and ERG, two closely-related proteins, bind, as do all the ETS proteins characterized so far, to DNA sequences with an invariable central GGA core flanked by preferred nucleotides. Nevertheless, promoter-specific responses to FLI or ERG may be driven by mechanisms involving multicomponent complexes. Using a yeast two-hybrid screen, we have identified several proteins that physically interact with either FLI or ERG proteins used as bait. The Xenopus developmentally implicated Xvent-2 and Xvent-2B proteins, and the Xenopus splicing factor RNP-C/U1C physically interact with Xl-FLI and Xl-ERG, both in the yeast two-hybrid system and in vitro. We also report the potential interaction of FLI and ERG with Sox-D, a stabilizing protein that may modulate their transcriptional activity. Furthermore, the possible involvement of the transcriptional effectors FLI and ERG in mRNA processing, hematopoiesis or in the control of angiogenesis is suggested through possible interactions with, respectively, RNA binding proteins and hnRNPs, a repressor of the hematopoietic pathway (SAP18), and the HAF protein.
Fli和erg是ETS基因家族的两个成员,该家族编码与c-ets-1原癌基因相关的转录因子。ETS基因的产物在细胞增殖、分化和致癌转化中起转录效应子的作用。FLI和ERG这两种密切相关的蛋白质,与迄今为止所鉴定的所有ETS蛋白质一样,都能结合到具有不变的中央GGA核心且两侧为优选核苷酸的DNA序列上。然而,对FLI或ERG的启动子特异性反应可能由涉及多组分复合物的机制驱动。通过酵母双杂交筛选,我们鉴定出了几种与用作诱饵的FLI或ERG蛋白发生物理相互作用的蛋白质。非洲爪蟾发育相关的Xvent-2和Xvent-2B蛋白,以及非洲爪蟾剪接因子RNP-C/U1C,在酵母双杂交系统和体外均与Xl-FLI和Xl-ERG发生物理相互作用。我们还报道了FLI和ERG与Sox-D的潜在相互作用,Sox-D是一种可能调节它们转录活性的稳定蛋白。此外,通过分别与RNA结合蛋白和hnRNPs、造血途径的一种阻遏物(SAP18)以及HAF蛋白的可能相互作用,提示转录效应子FLI和ERG可能参与mRNA加工、造血或血管生成的调控。