Li Y, Lau L F
Department of Genetics, University of Illinois College of Medicine, Chicago 60607-7170, USA.
Endocrinology. 1997 Oct;138(10):4138-46. doi: 10.1210/endo.138.10.5464.
ACTH treatment of Y1 adrenocortical cells induces the synthesis of Nur77, an orphan nuclear receptor that can act as a potent transactivator for such genes as 21-hydroxylase (CYP21). Nur77 has thus been proposed to be a mediator of ACTH action in activating the expression of genes that encode steroidogenic enzymes. Here we show that ACTH regulates the activity of Nur77 at the level of phosphorylation. ACTH induces the synthesis of transcriptionally active, DNA-binding Nur77 that is unphosphorylated at Ser354, which resides within the DNA-binding domain. By contrast, the Nur77 population that is constitutively present in Y1 cells is phosphorylated at Ser354 and does not bind DNA. Substitutions of Ser354 with negatively charged amino acids, such as Asp or Glu, dramatically decreased Nur77 DNA-binding and trans-activation activities, whereas mutation to the neutral Ala had no effect. Aside from phosphorylation within the DNA-binding domain, ACTH treatment does not induce modifications in the N- and C-terminal domains of Nur77 that significantly affect activity. Although the specific kinases that phosphorylate Nur77 in vivo are not known, the mitogen-activated protein kinase/pp90RSK pathway is not critical to Nur77 regulation. We propose that ACTH treatment of Y1 cells results in modulation of the activities of both kinases and phosphatases, which, in turn, regulate the activities of such transcription factors as Nur77.
促肾上腺皮质激素(ACTH)对Y1肾上腺皮质细胞的处理可诱导Nur77的合成,Nur77是一种孤儿核受体,可作为21-羟化酶(CYP21)等基因的有效反式激活因子。因此,Nur77被认为是ACTH在激活编码类固醇生成酶基因表达过程中的作用介质。在此我们表明,ACTH在磷酸化水平上调节Nur77的活性。ACTH诱导合成转录活性的、与DNA结合的Nur77,其在位于DNA结合域内的Ser354处未被磷酸化。相比之下,Y1细胞中组成性存在的Nur77群体在Ser354处被磷酸化且不与DNA结合。用带负电荷的氨基酸(如Asp或Glu)取代Ser354会显著降低Nur77的DNA结合和反式激活活性,而突变为中性的Ala则没有影响。除了DNA结合域内的磷酸化外,ACTH处理不会诱导Nur77的N端和C端结构域发生显著影响活性的修饰。虽然体内磷酸化Nur77的具体激酶尚不清楚,但丝裂原活化蛋白激酶/pp90RSK途径对Nur77的调节并不关键。我们提出,ACTH对Y1细胞的处理导致激酶和磷酸酶活性的调节,进而调节诸如Nur77等转录因子的活性。