Kim Young-Mi, Watanabe Takuo, Allen Patrick B, Kim Young-Myoung, Lee Shin-Jeong, Greengard Paul, Nairn Angus C, Kwon Young-Guen
Department of Biochemistry, College of Natural Sciences, Kangwon National University, Chunchon, Kangwon-Do 200-701, Korea.
J Biol Chem. 2003 Apr 18;278(16):13819-28. doi: 10.1074/jbc.M209621200. Epub 2003 Feb 6.
PNUTS, Phosphatase 1 NUclear Targeting Subunit, is a recently described protein that targets protein phosphatase 1 (PP1) to the nucleus. In the present study, we characterized the biochemical properties of PNUTS. A variety of truncation and site-directed mutants of PNUTS was prepared and expressed either as glutathione S-transferase fusion proteins in Escherichia coli or as FLAG-tagged proteins in 293T cells. A 50-amino acid domain in the center of PNUTS mediated both high affinity PP1 binding and inhibition of PP1 activity. The PP1-binding domain is related to a motif found in several other PP1-binding proteins but is distinct in that Trp replaces Phe. Mutation of the Trp residue essentially abolished the ability of PNUTS to bind to and inhibit PP1. The central PP1-binding domain of PNUTS was an effective substrate for protein kinase A in vitro, and phosphorylation substantially reduced the ability of PNUTS to bind to PP1 in vitro and following stimulation of protein kinase A in intact cells. In vitro RNA binding experiments showed that a C-terminal region including several RGG motifs and a novel repeat domain rich in His and Gly interacted with mRNA and single-stranded DNA. PNUTS exhibited selective binding for poly(A) and poly(G) compared with poly(U) or poly(C) ribonucleotide homopolymers, with specificity being mediated by distinct regions within the domain rich in His and Gly and the domain containing the RGG motifs. Finally, a PNUTS-PP1 complex was isolated from mammalian cell lysates using RNA-conjugated beads. Together, these studies support a role for PNUTS in protein kinase A-regulated targeting of PP1 to specific RNA-associated complexes in the nucleus.
PNUTS,即磷酸酶1核靶向亚基,是一种最近被描述的可将蛋白磷酸酶1(PP1)靶向至细胞核的蛋白质。在本研究中,我们对PNUTS的生化特性进行了表征。制备了多种PNUTS的截短突变体和定点突变体,并将其作为谷胱甘肽S-转移酶融合蛋白在大肠杆菌中表达,或作为FLAG标签蛋白在293T细胞中表达。PNUTS中央的一个50个氨基酸的结构域介导了与PP1的高亲和力结合以及对PP1活性的抑制。PP1结合结构域与在其他几种PP1结合蛋白中发现的一个基序相关,但不同之处在于色氨酸取代了苯丙氨酸。色氨酸残基的突变基本上消除了PNUTS结合和抑制PP1的能力。PNUTS的中央PP1结合结构域在体外是蛋白激酶A的有效底物,磷酸化显著降低了PNUTS在体外以及完整细胞中受到蛋白激酶A刺激后与PP1结合的能力。体外RNA结合实验表明,一个包含几个RGG基序和一个富含组氨酸和甘氨酸的新型重复结构域的C末端区域与mRNA和单链DNA相互作用。与聚尿苷酸或聚胞苷酸核糖核苷酸均聚物相比,PNUTS对聚腺苷酸和聚鸟苷酸表现出选择性结合,其特异性由富含组氨酸和甘氨酸的结构域以及包含RGG基序的结构域内的不同区域介导。最后,使用RNA偶联磁珠从哺乳动物细胞裂解物中分离出了PNUTS-PP1复合物。总之,这些研究支持了PNUTS在蛋白激酶A调节的将PP1靶向至细胞核中特定RNA相关复合物过程中的作用。