Unité de Glycobiologie Structurale et Fonctionnelle, UMR 8576 CNRS-Université des Sciences et Technologies de Lille, IFR 148, 59655 Villeneuve d'Ascq, France.
Biochem Cell Biol. 2012 Jun;90(3):307-19. doi: 10.1139/o11-070. Epub 2012 Feb 9.
Delta-lactoferrin (ΔLf) is a transcription factor of which the expression is downregulated in cancer. It is a healthy tissue marker and a high expression level of its transcripts was correlated with a good prognosis in breast cancer. ΔLf results from alternative promoter usage of the hLf gene leading to the production of 2 isoforms with alternative N-termini: lactoferrin, which is secreted, and ΔLf, its nucleocytoplasmic counterpart. ΔLf possesses antiproliferative properties and induces cell cycle arrest. It is an efficient transcription factor interacting in vivo via a ΔLf response element found in the Skp1, Bax, DcpS, and SelH promoters. Since ΔLf possesses different target genes, modifications in its activity or concentration may have crucial effects on cell homeostasis. Posttranslational modifications modulate ΔLf transcription factor activity. Our earlier investigations showed that O-GlcNAcylation negatively regulates ΔLf transcriptional activity, whilst inhibiting its ubiquitination and increasing its half-life. On the other hand, phosphorylation potentiates ΔLf transcriptional activity. Recently, we showed that ΔLf is also modified by SUMOylation. Therefore, cooperation and (or) competition among SUMOylation, ubiquitination, phosphorylation, and O-GlcNAcylation may contribute to the establishment of a fine regulation of ΔLf transcriptional activity depending on the type of target gene and cellular homeostasis.
δ-乳白蛋白(ΔLf)是一种转录因子,其在癌症中的表达受到下调。它是一种健康组织标志物,其转录本的高表达水平与乳腺癌的良好预后相关。ΔLf 是由 hLf 基因的选择性启动子使用导致的,产生具有不同 N 末端的 2 种同工型:分泌型乳白蛋白和核质型 ΔLf。ΔLf 具有抗增殖特性,并诱导细胞周期停滞。它是一种有效的转录因子,通过体内发现的 Skp1、Bax、DcpS 和 SelH 启动子中的 ΔLf 反应元件进行相互作用。由于 ΔLf 具有不同的靶基因,其活性或浓度的改变可能对细胞内稳态产生关键影响。翻译后修饰调节 ΔLf 转录因子的活性。我们之前的研究表明,O-GlcNAcylation 负调控 ΔLf 的转录活性,同时抑制其泛素化并增加其半衰期。另一方面,磷酸化增强了 ΔLf 的转录活性。最近,我们发现 ΔLf 还被 SUMOylation 修饰。因此,SUMOylation、泛素化、磷酸化和 O-GlcNAcylation 之间的合作和(或)竞争可能有助于根据靶基因的类型和细胞内稳态建立对 ΔLf 转录活性的精细调节。