Cluning Carmel, Ward Bryan K, Rea Sarah L, Arulpragasam Ajanthy, Fuller Peter J, Ratajczak Thomas
Laboratory for Molecular Endocrinology, Western Australian Institute forMedical Research and the UWA Centre for Medical Research, The University of Western Australia, Australia.
Mol Endocrinol. 2013 Jul;27(7):1020-35. doi: 10.1210/me.2012-1023. Epub 2013 May 17.
The heat-shock protein 90 (Hsp90) cochaperone FK506-binding protein 52 (FKBP52) upregulates, whereas FKBP51 inhibits, hormone binding and nuclear targeting of the glucocorticoid receptor (GR). Decreased cortisol sensitivity in the guinea pig is attributed to changes within the helix 1 to helix 3 (H1-H3) loop of the guinea pig GR (gpGR) ligand-binding domain. It has been proposed that this loop serves as a contact point for FKBP52 and/or FKBP51 with receptor. We examined the role of the H1-H3 loop in GR activation by FKBP52 using a Saccharomyces cerevisiae model. The activity of rat GR (rGR) containing the gpGR H1-H3 loop substitutions was still potentiated by FKBP52, confirming the loop is not involved in primary FKBP52 interactions. Additional assays also excluded a role for other intervening loops between ligand-binding domain helices in direct interactions with FKBP52 associated with enhanced receptor activity. Complementary studies in FKBP51-deficient mouse embryo fibroblasts and HEK293 cells demonstrated that substitution of the gpGR H1-H3 loop residues into rGR dramatically increased receptor repression by FKBP51 without enhancing receptor-FKBP51 interaction and did not alter recruitment of endogenous Hsp90 and the p23 cochaperone to receptor complexes. FKBP51 suppression of the mutated rGR did not require FKBP51 peptidylprolyl cis-trans isomerase activity and was not disrupted by mutation of the FK1 proline-rich loop thought to mediate reciprocal FKBP influences on receptor activity. We conclude that the gpGR-specific mutations within the H1-H3 loop confer global changes within the GR-Hsp90 complex that favor FKBP51 repression over FKBP52 potentiation, thus identifying the loop as an important target for GR regulation by the FKBP cochaperones.
热休克蛋白90(Hsp90)的共伴侣FK506结合蛋白52(FKBP52)可上调糖皮质激素受体(GR)的激素结合及核靶向作用,而FKBP51则起抑制作用。豚鼠体内皮质醇敏感性降低归因于豚鼠GR(gpGR)配体结合域中螺旋1至螺旋3(H1-H3)环内的变化。有人提出,该环是FKBP52和/或FKBP51与受体的接触点。我们使用酿酒酵母模型研究了H1-H3环在FKBP52激活GR中的作用。含有gpGR H1-H3环替代物的大鼠GR(rGR)活性仍被FKBP52增强,这证实该环不参与FKBP52的主要相互作用。其他试验还排除了配体结合域螺旋之间的其他中间环在与增强受体活性相关的FKBP52直接相互作用中的作用。在FKBP51缺陷的小鼠胚胎成纤维细胞和HEK293细胞中的补充研究表明,将gpGR H1-H3环残基替换到rGR中会显著增加FKBP51对受体的抑制作用,而不会增强受体与FKBP51的相互作用,也不会改变内源性Hsp90和p23共伴侣向受体复合物的募集。FKBP51对突变rGR的抑制作用不需要FKBP51肽基脯氨酰顺反异构酶活性,也不会因FK1富含脯氨酸的环突变而受到干扰,该环被认为介导FKBP对受体活性的相互影响。我们得出结论,H1-H3环内的gpGR特异性突变在GR-Hsp90复合物中产生全局性变化,有利于FKBP51的抑制作用而非FKBP52的增强作用,从而确定该环是FKBP共伴侣调节GR的重要靶点。