Graduate School of Life Science, Hokkaido University, Sapporo, Japan; Faculty of Science, Hokkaido University, Sapporo, Japan.
Graduate School of Life Science, Hokkaido University, Sapporo, Japan.
J Steroid Biochem Mol Biol. 2021 Jun;210:105845. doi: 10.1016/j.jsbmb.2021.105845. Epub 2021 Feb 27.
Orthologs of human glucocorticoid receptor (GR) and human mineralocorticoid receptor (MR) first appear in cartilaginous fishes. Subsequently, the MR and GR diverged to respond to different steroids: the MR to aldosterone and the GR to cortisol and corticosterone. We report that cortisol, corticosterone and aldosterone activate full-length elephant shark GR, and progesterone, which activates elephant shark MR, does not activate elephant shark GR. However, progesterone inhibits steroid binding to elephant shark GR, but not to human GR. Together, this indicates partial functional divergence of elephant shark GR from the MR. Deletion of the N-terminal domain (NTD) from elephant shark GR (truncated GR) reduced the response to corticosteroids, while truncated and full-length elephant shark MR had similar responses to corticosteroids. Swapping of NTDs of elephant shark GR and MR yielded an elephant shark MR chimera with full-length GR-like increased activation by corticosteroids and progesterone compared to full-length elephant shark MR. Elephant shark MR NTD fused to GR DBD + LBD had similar activation as full-length MR, indicating that the MR NTD lacked GR-like NTD activity. We propose that NTD activation of human GR evolved early in GR divergence from the MR.
人类糖皮质激素受体 (GR) 和人类盐皮质激素受体 (MR) 的同源物首先出现在软骨鱼类中。随后,MR 和 GR 分化以响应不同的类固醇:MR 对醛固酮,GR 对皮质醇和皮质酮。我们报告称,皮质醇、皮质酮和醛固酮激活全长象鲨 GR,而激活象鲨 MR 的孕酮不激活象鲨 GR。然而,孕酮抑制类固醇与象鲨 GR 的结合,但不与人类 GR 结合。总之,这表明象鲨 GR 从 MR 中部分功能分化。从象鲨 GR 中删除 N 端结构域(NTD)(截断 GR)降低了对皮质类固醇的反应,而截断和全长象鲨 MR 对皮质类固醇有相似的反应。象鲨 GR 和 MR 的 NTD 交换产生了一种象鲨 MR 嵌合体,与全长象鲨 MR 相比,全长 GR 样增加了对皮质类固醇和孕酮的激活。与全长 MR 相似,象鲨 MR NTD 融合到 GR DBD + LBD 上具有相似的激活作用,表明 MR NTD 缺乏 GR 样 NTD 活性。我们提出,人类 GR 的 NTD 激活在 GR 从 MR 分化的早期就进化了。