Maki Akio, Sawatsubashi Shun, Ito Saya, Shirode Yuko, Suzuki Eriko, Zhao Yue, Yamagata Kaoru, Kouzmenko Alexander, Takeyama Ken-Ichi, Kato Shigeaki
The Institute of Molecular and Cellular Biosciences, University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.
Biochem Biophys Res Commun. 2004 Jul 16;320(1):262-7. doi: 10.1016/j.bbrc.2004.05.156.
Insect development is controlled by the combined actions of ecdysteroid and juvenile hormones. Transcriptional control by ecdysteroid hormones is mediated via two nuclear receptor superfamily members, ecdysone receptor (EcR) and its heterodimeric partner, ultraspiracle (USP). Although the ecdysteroid hormone 20-hydroxyecdysone acts as an EcR ligand and activates transcription through EcR/USP heterodimers, the activity of juvenile hormones, such as Juvenile hormone III (JH III), and methoprenic acid (MA) via USP remains unclear. Here, we demonstrate that juvenile hormones act as USP ligands and exhibit suppressive effects on ecdysone-dependent EcR transactivation. JH III- and MA-bound USP markedly repressed ecdysone-dependent EcR transactivation through shifting of the USP ligand-binding domain alpha-helix 12 without affecting EcR/USP heterodimerization or DNA binding. Moreover, transcriptional repression by USP ligands was attenuated by a histone deacetylation inhibitor. Our results suggested that juvenile hormones serve as USP ligands that antagonize EcR-mediated ecdysone actions through the recruitment of histone deacetylase complexes.
昆虫发育受蜕皮甾类激素和保幼激素的共同作用控制。蜕皮甾类激素的转录调控是通过两个核受体超家族成员介导的,即蜕皮激素受体(EcR)及其异源二聚体伴侣超气门蛋白(USP)。尽管蜕皮甾类激素20-羟基蜕皮酮作为EcR配体并通过EcR/USP异源二聚体激活转录,但保幼激素如保幼激素III(JH III)和烯虫酯酸(MA)通过USP发挥的活性仍不清楚。在此,我们证明保幼激素作为USP配体,并对蜕皮激素依赖的EcR反式激活具有抑制作用。结合JH III和MA的USP通过USP配体结合域α-螺旋12的移位显著抑制蜕皮激素依赖的EcR反式激活,而不影响EcR/USP异源二聚化或DNA结合。此外,组蛋白去乙酰化酶抑制剂减弱了USP配体的转录抑制作用。我们的结果表明,保幼激素作为USP配体,通过募集组蛋白去乙酰化酶复合物拮抗EcR介导的蜕皮激素作用。