Suppr超能文献

蛋白激酶A对维甲酸受体α的磷酸化作用。

Phosphorylation of the retinoic acid receptor-alpha by protein kinase A.

作者信息

Rochette-Egly C, Oulad-Abdelghani M, Staub A, Pfister V, Scheuer I, Chambon P, Gaub M P

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique/INSERM, Université Louis Pasteur/Collège de France, Illkirch, C.U. de Strasbourg.

出版信息

Mol Endocrinol. 1995 Jul;9(7):860-71. doi: 10.1210/mend.9.7.7476969.

Abstract

The phosphorylation of retinoic acid receptor-alpha 1 (RAR alpha 1) by PKA was investigated both in vitro and in vivo. We show that bacterially expressed RAR alpha 1 is phosphorylated in vitro by protein kinase A (PKA) at the unique serine residue 369 located in the C-terminal end of the E region. We also show that RAR alpha 1 overexpressed in COS-1 cells is phosphorylated on multiple serine residues and that phosphorylation at serine 369 occurs only when COS-1 cells are cotransfected with PKA or treated with forskolin. RAR alpha 1 mutants were constructed in which serine 369 was replaced by an alanine (S369A) or a glutamic acid (S369E) residue. Comparison of the tryptic phosphopeptide patterns of wild type and mutated RAR alpha 1 overexpressed in COS-1 cells allowed us to confirm that serine 369 is the unique phosphorylation site for PKA in cultured cells. The DNA-binding efficiency of RAR alpha/retinoid X receptor-alpha (RXR alpha) heterodimers was enhanced in vitro by the S369E mutation. However, in transfected RAC65 cells, the same S369E mutation did not affect the ligand-dependent transcriptional activation by RAR alpha 1 of reporter genes containing a retinoic acid (RA)-response element. In contrast, the S369A mutation slightly decreased both DNA binding and the efficiency of PKA to enhance RA-induced transactivation by RAR alpha 1. Finally, we show that endogenous RAR alpha is also phosphorylated in vivo at serine 369 in forskolin-treated F9 cells, supporting the idea that phosphorylation of RARs at this site is involved in the modulation of the RA-induced differentiation of F9 cells by (Bu)2cAMP.

摘要

我们在体外和体内研究了蛋白激酶A(PKA)对维甲酸受体α1(RARα1)的磷酸化作用。我们发现,细菌表达的RARα1在体外被蛋白激酶A(PKA)磷酸化,磷酸化位点是位于E区域C末端的独特丝氨酸残基369。我们还发现,在COS-1细胞中过表达的RARα1在多个丝氨酸残基上被磷酸化,并且只有当COS-1细胞与PKA共转染或用福司可林处理时,丝氨酸369才会发生磷酸化。构建了RARα1突变体,其中丝氨酸369被丙氨酸(S369A)或谷氨酸(S369E)残基取代。通过比较在COS-1细胞中过表达的野生型和突变型RARα1的胰蛋白酶磷酸肽图谱,我们证实丝氨酸369是培养细胞中PKA的唯一磷酸化位点。S369E突变在体外增强了RARα/维甲酸X受体α(RXRα)异二聚体的DNA结合效率。然而,在转染的RAC65细胞中,相同的S369E突变并不影响含有视黄酸(RA)反应元件的报告基因的RARα1的配体依赖性转录激活。相反,S369A突变略微降低了DNA结合以及PKA增强RARα1诱导的RA转录激活的效率。最后,我们表明,在福司可林处理的F9细胞中,内源性RARα在体内也在丝氨酸369处被磷酸化,这支持了RARs在此位点的磷酸化参与(Bu)2cAMP对RA诱导的F9细胞分化的调节这一观点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验