Wang Dantong, De Deken Xavier, Milenkovic Milutin, Song Yue, Pirson Isabelle, Dumont Jacques E, Miot Françoise
Institut de Recherche Interdisciplinaire, Université Libre De Bruxelles, Campus Erasme, 808, route de Lennik, 1070 Bruxelles, Belgium.
J Biol Chem. 2005 Jan 28;280(4):3096-103. doi: 10.1074/jbc.M407709200. Epub 2004 Nov 22.
H(2)O(2) is a crucial substrate of thyroproxidase (TPO) to iodinate thyroglobulin and synthesize thyroid hormones in thyroid. ThOX proteins (thyroid oxidase) also called Duox are believed to be responsible for H(2)O(2) generation. Duoxs expressed in transfected cells do not generate an active system, nor permit their membrane localization suggesting that other proteins are required to fulfill these functions. In this study, we demonstrate interactions of Duoxs with TPO and with p22(phox) without any effect on Duox activity. By yeast two-hybrid method using EF-hand fragment of dog Duox1 as the bait we have isolated EFP1 (EF-hand binding protein 1), one partner of Duoxs that belongs to the thioredoxin-related protein family. EFP1 shares moderate similarities with other members of thioredoxin-related proteins, but the characteristic active site and the folding structures are well conserved. EFP1 can be co-immunoprecipitated with Duoxs in transfected COS cells as well as in primary cultured human thyrocytes. It interacts also with TPO but not thyroglobulin. Immunofluorescence studies show that EFP1 and Duox proteins are co-localized inside the transfected cells, suggesting that EFP1 is not sufficient to induce either the expression of Duox at the plasma membrane or to permit H(2)O(2) production. EFP1 and Duox mRNA share similar distribution in nine different tissues. These results suggest that EFP1 could be one of the partners in the assembly of the multiprotein complex constituting the thyroid H(2)O(2) generating system but is certainly not sufficient to permit H(2)O(2) generation.
H₂O₂是甲状腺过氧化物酶(TPO)碘化甲状腺球蛋白并在甲状腺中合成甲状腺激素的关键底物。ThOX蛋白(甲状腺氧化酶)也称为Duox,被认为负责H₂O₂的产生。在转染细胞中表达的Duox不会产生活性系统,也不允许其膜定位,这表明需要其他蛋白质来完成这些功能。在本研究中,我们证明了Duox与TPO以及与p22phox之间的相互作用,而对Duox活性没有任何影响。通过酵母双杂交方法,以犬Duox1的EF-手型片段为诱饵,我们分离出了EFP1(EF-手型结合蛋白1),它是Duox的一个伴侣,属于硫氧还蛋白相关蛋白家族。EFP1与硫氧还蛋白相关蛋白的其他成员有中等程度的相似性,但其特征性的活性位点和折叠结构保存完好。在转染的COS细胞以及原代培养的人甲状腺细胞中,EFP1可以与Duox进行共免疫沉淀。它也与TPO相互作用,但不与甲状腺球蛋白相互作用。免疫荧光研究表明,EFP1和Duox蛋白在转染细胞内共定位,这表明EFP1不足以诱导Duox在质膜上的表达或产生H₂O₂。EFP1和Duox mRNA在九种不同组织中具有相似的分布。这些结果表明,EFP1可能是构成甲状腺H₂O₂生成系统的多蛋白复合物组装中的伴侣之一,但肯定不足以允许H₂O₂的产生。