Choi Hack Sun, Kim Chun Sung, Hwang Cheol Kyu, Song Kyu Young, Law Ping-Yee, Wei Li-Na, Loh Horace H
Department of Pharmacology, University of Minnesota Medical School, 6-120 Jackson Hall, 321 Church St. SE, Minneapolis, MN 55455, USA.
FASEB J. 2007 Dec;21(14):3963-73. doi: 10.1096/fj.07-8561com. Epub 2007 Jul 11.
The alpha-complex proteins (alphaCP) are generally known as RNA-binding proteins that interact in a sequence-specific fashion with single-stranded poly(C). These proteins are mainly involved in various post-transcriptional regulations (e.g., mRNA stabilization or translational activation/silencing). Here we report a novel function of alphaCP3, a member of the alphaCP family. alphaCP3 bound to the double-stranded poly(C) element essential for the mu opioid receptor (MOR) promoter and repressed the promoter activity at the transcriptional level. We identified alphaCP3 using affinity column chromatography containing the double-stranded poly(C) element and matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry. AlphaCP3 binding to the poly(C) sequence of the MOR gene was sequence specific, as confirmed by the supershift assay. In cotransfection studies, alphaCP3 repressed the MOR promoter only when the poly(C) sequence was intact. Ectopic expression of alphaCP3 led to repression of the endogenous MOR transcripts in NS20Y cells. When alphaCP3 was disrupted using small interfering RNA (siRNA) in NS20Y cells, the transcription of the endogenous target MOR gene was increased significantly. Our data suggest that alphaCP3 can function as a repressor of MOR transcription dependent on the MOR poly(C) sequence. We demonstrate for the first time a role of alphaCP3 as a transcriptional repressor in MOR gene regulation.
α-复合蛋白(αCP)通常被认为是一类RNA结合蛋白,它们以序列特异性方式与单链聚(C)相互作用。这些蛋白主要参与各种转录后调控(例如,mRNA稳定或翻译激活/沉默)。在此,我们报道了αCP家族成员αCP3的一种新功能。αCP3与μ阿片受体(MOR)启动子所必需的双链聚(C)元件结合,并在转录水平上抑制启动子活性。我们使用含有双链聚(C)元件的亲和柱色谱法和基质辅助激光解吸电离飞行时间(MALDI-TOF)质谱法鉴定了αCP3。超迁移分析证实,αCP3与MOR基因的聚(C)序列结合具有序列特异性。在共转染研究中,只有当聚(C)序列完整时,αCP3才会抑制MOR启动子。αCP3的异位表达导致NS20Y细胞中内源性MOR转录本的抑制。当在NS20Y细胞中使用小干扰RNA(siRNA)破坏αCP3时,内源性靶标MOR基因的转录显著增加。我们的数据表明,αCP3可以作为依赖于MOR聚(C)序列的MOR转录抑制因子发挥作用。我们首次证明了αCP3作为转录抑制因子在MOR基因调控中的作用。