Lavens Delphine, Montoye Tony, Piessevaux Julie, Zabeau Lennart, Vandekerckhove Joël, Gevaert Kris, Becker Walter, Eyckerman Sven, Tavernier Jan
Department of Medical Protein Research, Faculty of Medicine and Health Sciences, Flanders Interuniversity Institute for Biotechnology, VIB09, Ghent University, Belgium.
J Cell Sci. 2006 Jun 1;119(Pt 11):2214-24. doi: 10.1242/jcs.02947. Epub 2006 May 9.
Hypothalamic leptin receptor signalling plays a central role in weight regulation by controlling fat storage and energy expenditure. In addition, leptin also has direct effects on peripheral cell types involved in regulation of diverse body functions including immune response, bone formation and reproduction. Previous studies have demonstrated the important role of SOCS3 (suppressor of cytokine signalling 3) in leptin physiology. Here, we show that CIS (cytokine-inducible SH2 protein) and SOCS2 can also interact with the leptin receptor. Using MAPPIT (mammalian protein-protein interaction trap), a cytokine receptor-based two-hybrid method operating in intact cells, we show specific binding of CIS with the conserved Y985 and Y1077 motifs in the cytosolic domain of the leptin receptor. SOCS2 only interacts with the Y1077 motif, but with higher binding affinity and can interfere with CIS and STAT5a prey recruitment at this site. Furthermore, although SOCS2 does not associate with Y985 of the leptin receptor, we find that SOCS2 can block interaction of CIS with this position. This unexpected interference can be explained by the direct binding of SOCS2 on the CIS SOCS box, whereby elongin B/C recruitment is crucial to suppress CIS activity.
下丘脑瘦素受体信号传导通过控制脂肪储存和能量消耗在体重调节中起核心作用。此外,瘦素对参与多种身体功能调节的外周细胞类型也有直接影响,这些功能包括免疫反应、骨形成和生殖。先前的研究已经证明细胞因子信号传导抑制因子3(SOCS3)在瘦素生理学中的重要作用。在此,我们表明细胞因子诱导的SH2蛋白(CIS)和SOCS2也能与瘦素受体相互作用。使用哺乳动物蛋白-蛋白相互作用陷阱(MAPPIT),一种在完整细胞中起作用的基于细胞因子受体的双杂交方法,我们展示了CIS与瘦素受体胞质结构域中保守的Y985和Y1077基序的特异性结合。SOCS2仅与Y1077基序相互作用,但结合亲和力更高,并且可以在该位点干扰CIS和信号转导和转录激活因子5a(STAT5a)的猎物募集。此外,虽然SOCS2不与瘦素受体的Y985结合,但我们发现SOCS2可以阻断CIS与该位点的相互作用。这种意外的干扰可以通过SOCS2直接结合在CIS的SOCS盒上来解释,由此,延伸蛋白B/C的募集对于抑制CIS活性至关重要。