Lu Jia Yang, Sewer Marion B
Skaggs School of Pharmacy & Pharmaceutical Sciences, University of California, San Diego, La Jolla, California, USA.
Skaggs School of Pharmacy & Pharmaceutical Sciences, University of California, San Diego, La Jolla, California, USA
Mol Cell Biol. 2015 Apr;35(7):1223-37. doi: 10.1128/MCB.00993-14. Epub 2015 Jan 20.
Glucocorticoid production in the adrenal cortex is activated in response to an increase in cyclic AMP (cAMP) signaling. The nuclear protein p54(nrb)/NONO belongs to the Drosophila behavior/human splicing (DBHS) family and has been implicated in several nuclear processes, including transcription, splicing, and RNA export. We previously identified p54(nrb)/NONO as a component of a protein complex that regulates the transcription of CYP17A1, a gene required for glucocorticoid production. Based on the multiple mechanisms by which p54(nrb)/NONO has been shown to control gene expression and the ability of the protein to be recruited to the CYP17A1 promoter, we sought to further define the molecular mechanism by which p54(nrb)/NONO confers optimal cortisol production. We show here that silencing p54(nrb)/NONO expression in H295R human adrenocortical cells decreases the ability of the cells to increase intracellular cAMP production and subsequent cortisol biosynthesis in response to adrenocorticotropin hormone (ACTH) stimulation. Interestingly, the expression of multiple phosphodiesterase (PDE) isoforms, including PDE2A, PDE3A, PDE3B, PDE4A, PDE4D, and PDE11A, was induced in p54(nrb)/NONO knockdown cells. Investigation of the mechanism by which silencing of p54(nrb)/NONO led to increased expression of select PDE isoforms revealed that p54(nrb)/NONO regulates the splicing of a subset of PDE isoforms. Importantly, we also identify a role for p54(nrb)/NONO in regulating the stability of PDE transcripts by facilitating the interaction between the exoribonuclease XRN2 and select PDE transcripts. In summary, we report that p54(nrb)/NONO modulates cAMP-dependent signaling, and ultimately cAMP-stimulated glucocorticoid biosynthesis by regulating the splicing and degradation of PDE transcripts.
肾上腺皮质中糖皮质激素的产生会因环磷酸腺苷(cAMP)信号增加而被激活。核蛋白p54(nrb)/NONO属于果蝇行为/人类剪接(DBHS)家族,参与了包括转录、剪接和RNA输出在内的多个核过程。我们之前鉴定出p54(nrb)/NONO是一种蛋白质复合物的组成成分,该复合物可调节CYP17A1的转录,CYP17A1是糖皮质激素产生所需的基因。基于已证明p54(nrb)/NONO控制基因表达的多种机制以及该蛋白被招募至CYP17A1启动子的能力,我们试图进一步明确p54(nrb)/NONO赋予最佳皮质醇产生的分子机制。我们在此表明,沉默H295R人肾上腺皮质细胞中的p54(nrb)/NONO表达会降低细胞响应促肾上腺皮质激素(ACTH)刺激而增加细胞内cAMP产生及随后皮质醇生物合成的能力。有趣的是,在p54(nrb)/NONO敲低细胞中诱导了多种磷酸二酯酶(PDE)亚型的表达,包括PDE2A、PDE3A、PDE3B、PDE4A、PDE4D和PDE11A。对p54(nrb)/NONO沉默导致特定PDE亚型表达增加的机制进行研究发现,p54(nrb)/NONO调节一部分PDE亚型的剪接。重要的是,我们还确定了p54(nrb)/NONO在通过促进外切核糖核酸酶XRN2与特定PDE转录本之间的相互作用来调节PDE转录本稳定性方面的作用。总之,我们报告p54(nrb)/NONO通过调节PDE转录本的剪接和降解来调节cAMP依赖性信号传导,并最终调节cAMP刺激的糖皮质激素生物合成。