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Atlas of Genetics and Cytogenetics in Oncology and Haematology OPEN ACCESS JOURNAL AT INIST-CNRS Gene Section Mini Review PPP2R4 (protein phosphatase 2A activator, regulatory subunit 4) Veerle Janssens Protein Phosphorylation and Proteomics Group, Department of Molecular Cell Biology, Faculty of Medicine, University of Leuven, Campus GHB O&N1, Herestraat 49, box 901, B-3000 Leuven, Belgium (VJ) Published in Atlas Database: February 2009 Online updated version: http://AtlasGeneticsOncology.org/Genes/PPP2R4ID41817ch9q34.html DOI: 10.4267/2042/44661 This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 2.0 France Licence. © 2010 Atlas of Genetics and Cytogenetics in Oncology and Haematology Identity (dolichyl pyrophosphate phosphatase 1), CRAT (carnitine acetyltransferase), PPP2R4, IER5L (immediate early response 5-like), C9orf106. Note In fact the gene name would be better: 'protein phosphatase 2A, regulatory subunit 4' or 'protein phosphatase 2A activator', and not a mixture of the two. Other names: MGC2184; OTTHUMP00000022333; PP2A; PR53; PTPA HGNC (Hugo): PPP2R4 Location: 9q34.11 Local order: From centromere to telomere: DOLPP1 DNA/RNA Figure 1. Schematic representation of PPP2R4 splice variants The top line represents the PPP2R4 gene. Exons are boxed (5' and 3' UTR are speckled). Introns and the 3' UTR are not drawn to scale. PTPA alpha and beta are the major transcripts/proteins; PTPA gamma, zeta and eta do not encode functional proteins and probably result from splicing errors. Gene promoter has been analyzed and resides in a non-methylated CpG island. No TATA or CAAT box. Two functional yin-yang-1 (YY1) binding sites direct basal promoter expression. Tumor suppressor p53 represses transcription through a mechanism involving YY1 inhibition Atlas Genet Cytogenet Oncol Haematol. 2010; 14(1) 48 PPP2R4 (protein phosphatase 2A activator, regulatory subunit 4) Janssens V Figure 2. Schematic structure of the PPP2R4 promoter Two YY1 sites are required for basal PPP2R4 promoter activity and reside within the minimal promoter (nt -67/+38 relative to the start of transcription which is at +1). Upstream of this minimal promoter a GC-rich Sp1-cluster is present (nt -670/-470) of which the functionality has not yet been proven. The PPP2R4 promoter resides within an unmethylated CpG island. Description Function The gene encompasses around 40 kb; 11 exons. Stimulates the phosphotyrosyl phosphatase activity of the PP2A core heterodimer in the presence of ATP/Mg2+ (in vitro). Reactivates the phosphoserine/threonine phospha-tase activity of an inactive PP2A form in the presence of ATP/Mg2+. This inactive PP2A is associated with the PP2A methylesterase (PME-1). peptidyl prolyl cis/trans ATP/Mg2+-dependent isomerase acting on Pro190 in the PP2A catalytic subunit. Binds to the PP2A heterodimeric core enzyme (A and C subunit). Required for the biogenesis of active PP2A. Reported to be pro- as well as anti-apoptotic. In Saccharomyces cerevisiae: two orthologues found. Involved in protection against oxidative damage, G1 progression, G2/M transition, Target of Rapamycin (TOR) pathway. Transcription Several transcripts have been identified, resulting from alternative splicing; two transcripts in Northern blot of human placental RNA with probe encompassing exons 1-10: 4.1 kb and 2.8 kb (likely resulting from the use of different polyadenylation signals). Alpha isoform: encompasses exons 1,2,3,5-11. Beta isoform: encompasses exons 1-11. Gamma isoform: encompasses exons 1,3-11. Delta isoform: encompasses exons 1,2,5-11. Epsilon isoform: encompasses exons 1,2,3,6-11. Zeta isoform: encompasses exons 1,3,5-11. Eta isoform: encompasses exons 1,5-11. Alpha, beta, delta, epsilon isoforms can be trans-lated into functional proteins in vitro; gamma, zeta, eta, are probably the result of splicing errors. Pseudogene None has been described. Protein Description Two isoforms detectable in Western blot of human placenta and several human cell lines: PTPA alpha, 323 amino acids, 36.8 kDa; PTPA beta, 358 amino acids, 40.7 kDa. pI around 5.8; trypsin-resistant. Expression Both isoforms are widely expressed. In a given cell line, PTPA alpha is about 10x more abundant than PTPA beta. Very high expression in p53-negative cell lines (for instance the osteosarcoma cell line Saos-2). Localisation Predominantly cytoplasmic. Atlas Genet Cytogenet Oncol Haematol. 2010; 14(1) Figure 3. PTPA protein structurePTPA is an all alpha-helical polypeptide, organized into two domains separated by a groove. Here the ribbon structure of human PTPA is displayed (derived from PDB code: 2IXM, Leulliot et al., 2006). 49 PPP2R4 (protein phosphatase 2A activator, regulatory subunit 4) Janssens V homologues from Drosophila melanogaster Saccharomyces cerevisiae. Biochemistry. 1998 15;37(37):12899-908 Homology No other human homologues known. Defines a new family of peptidyl prolyl cis/trans isomerases (PPIases) with all alpha-helical structure, organized into two domains separated by a groove. and Sep Janssens V, Van Hoof C, De Baere I, Merlevede W, Goris J. Functional analysis of the promoter region of the human phosphotyrosine phosphatase activator gene: Yin Yang 1 is essential for core promoter activity. Biochem J. 1999 Dec 15;344 Pt 3:755-63 To be noted Janssens V, Van Hoof C, De Baere I, Merlevede W, Goris J. The phosphotyrosyl phosphatase activator gene is a novel p53 target gene. J Biol Chem. 2000 Jul 7;275(27):20488-95 Note Although there is a huge and accumulating literature implicating PP2A in cancer etiology, PP2A enzymes represent a large and diverse family of holoenzymes, and the functional implications of specific complexes are only beginning to emerge. As such, it is clear that some PP2A holoenzymes may act as tumor suppressors, whereas others may on the contrary rather promote tumorigenesis. As for PPP2R4, one of the many cellular regulators/subunits of PP2A, there is as yet no direct evidence that this gene product is directly involved in these pathological processes. Janssens V, van Hoof C, Martens E, de Baere I, Merlevede W, Goris J. Identification and characterization of alternative splice products encoded by the human phosphotyrosyl phosphatase activator gene. Eur J Biochem. 2000 Jul;267(14):4406-13 Rempola B, Kaniak A, Migdalski A, Rytka J, Slonimski PP, di Rago JP. Functional analysis of RRD1 (YIL153w) and RRD2 (YPL152w), which encode two putative activators of the phosphotyrosyl phosphatase activity of PP2A in Saccharomyces cerevisiae. Mol Gen Genet. 2000 Jan;262(6):1081-92 Van Hoof C, Janssens V, De Baere I, de Winde JH, Winderickx J, Dumortier F, Thevelein JM, Merlevede W, Goris J. The Saccharomyces cerevisiae homologue YPA1 of the mammalian phosphotyrosyl phosphatase activator of protein phosphatase 2A controls progression through the G1 phase of the yeast cell cycle. J Mol Biol. 2000 Sep 8;302(1):103-20 References Cayla X, Goris J, Hermann J, Hendrix P, Ozon R, Merlevede W. Isolation and characterization of a tyrosyl phosphatase activator from rabbit skeletal muscle and Xenopus laevis oocytes. Biochemistry. 1990 Jan 23;29(3):658-67 Janssens V, Goris J. Protein phosphatase 2A: a highly regulated family of serine/threonine phosphatases implicated in cell growth and signalling. Biochem J. 2001 Feb 1;353(Pt 3):417-39 Cayla X, Van Hoof C, Bosch M, Waelkens E, Vandekerckhove J, Peeters B, Merlevede W, Goris J. Molecular cloning, expression, and characterization of PTPA, a protein that activates the tyrosyl phosphatase activity of protein phosphatase 2A. J Biol Chem. 1994 Jun 3;269(22):15668-75 Mitchell DA, Sprague GF Jr. The phosphotyrosyl phosphatase activator, Ncs1p (Rrd1p), functions with Cla4p to regulate the G(2)/M transition in Saccharomyces cerevisiae. Mol Cell Biol. 2001 Jan;21(2):488-500 Van Hoof C, Cayla X, Bosch M, Merlevede W, Goris J. The phosphotyrosyl phosphatase activator of protein phosphatase 2A. A novel purification method, immunological and enzymic characterization. Eur J Biochem. 1994 Dec 15;226(3):899-907 Rempola B, Kaniak A, di Rago JP, Rytka J. Anaerobic growth of Saccharomyces cerevisiae alleviates the lethal effect of phosphotyrosyl phosphatase activators depletion. Acta Biochim Pol. 2001;48(4):1043-9 Van Hoof C, Aly MS, Garcia A, Cayla X, Cassiman JJ, Merlevede W, Goris J. Structure and chromosomal localization of the human gene of the phosphotyrosyl phosphatase activator (PTPA) of protein phosphatase 2A. Genomics. 1995 Jul 20;28(2):261-72 Van Hoof C, Janssens V, De Baere I, Stark MJ, de Winde JH, Winderickx J, Thevelein JM, Merlevede W, Goris J. The Saccharomyces cerevisiae phosphotyrosyl phosphatase activator proteins are required for a subset of the functions disrupted by protein phosphatase 2A mutations. Exp Cell Res. 2001 Apr 1;264(2):372-87 Agostinis P, Donella-Deana A, Van Hoof C, Cesaro L, Brunati AM, Ruzzene M, Merlevede W, Pinna LA, Goris J. A comparative study of the phosphotyrosyl phosphatase specificity of protein phosphatase type 2A and phosphotyrosyl phosphatase type 1B using phosphopeptides and the phosphoproteins p50/HS1, c-Fgr and Lyn. Eur J Biochem. 1996 Mar 1;236(2):548-57 Fellner T, Lackner DH, Hombauer H, Piribauer P, Mudrak I, Zaragoza K, Juno C, Ogris E. A novel and essential mechanism determining specificity and activity of protein phosphatase 2A (PP2A) in vivo. Genes Dev. 2003 Sep 1;17(17):2138-50 Longin S, Jordens J, Martens E, Stevens I, Janssens V, Rondelez E, De Baere I, Derua R, Waelkens E, Goris J, Van Hoof C. An inactive protein phosphatase 2A population is associated with methylesterase and can be re-activated by the phosphotyrosyl phosphatase activator. Biochem J. 2004 May 15;380(Pt 1):111-9 Janssens V, Van Hoof C, Merlevede W, Goris J. PTPA regulating PP2A as a dual specificity phosphatase. Methods Mol Biol. 1998;93:103-15 Ramotar D, Belanger E, Brodeur I, Masson JY, Drobetsky EA. A yeast homologue of the human phosphotyrosyl phosphatase activator PTPA is implicated in protection against oxidative DNA damage induced by the model carcinogen 4nitroquinoline 1-oxide. J Biol Chem. 1998 Aug 21;273(34):21489-96 MacKeigan JP, Murphy LO, Blenis J. Sensitized RNAi screen of human kinases and phosphatases identifies new regulators of apoptosis and chemoresistance. Nat Cell Biol. 2005 Jun;7(6):591-600 Van Hoof C, Janssens V, Dinishiotu A, Merlevede W, Goris J. Functional analysis of conserved domains in the phosphotyrosyl phosphatase activator. Molecular cloning of the Atlas Genet Cytogenet Oncol Haematol. 2010; 14(1) Van Hoof C, Martens E, Longin S, Jordens J, Stevens I, Janssens V, Goris J. Specific interactions of PP2A and PP2Alike phosphatases with the yeast PTPA homologues, Ypa1 and Ypa2. Biochem J. 2005 Feb 15;386(Pt 1):93-102 50 PPP2R4 (protein phosphatase 2A activator, regulatory subunit 4) Janssens V Zheng Y, Jiang Y. The yeast phosphotyrosyl phosphatase activator is part of the Tap42-phosphatase complexes. Mol Biol Cell. 2005 Apr;16(4):2119-27 P. The crystal structure of a human PP2A phosphatase activator reveals a novel fold and highly conserved cleft implicated in protein-protein interactions. J Biol Chem. 2006 Aug 11;281(32):22434-8 Chao Y, Xing Y, Chen Y, Xu Y, Lin Z, Li Z, Jeffrey PD, Stock JB, Shi Y. Structure and mechanism of the phosphotyrosyl phosphatase activator. Mol Cell. 2006 Aug;23(4):535-46 Azam S, Drobetsky E, Ramotar D. Overexpression of the cis/trans isomerase PTPA triggers caspase 3-dependent apoptosis. Apoptosis. 2007 Jul;12(7):1243-55 Jordens J, Janssens V, Longin S, Stevens I, Martens E, Bultynck G, Engelborghs Y, Lescrinier E, Waelkens E, Goris J, Van Hoof C. The protein phosphatase 2A phosphatase activator is a novel peptidyl-prolyl cis/trans-isomerase. J Biol Chem. 2006 Mar 10;281(10):6349-57 Hombauer H, Weismann D, Mudrak I, Stanzel C, Fellner T, Lackner DH, Ogris E. Generation of active protein phosphatase 2A is coupled to holoenzyme assembly. PLoS Biol. 2007 Jun;5(6):e155 Leulliot N, Vicentini G, Jordens J, Quevillon-Cheruel S, Schiltz M, Barford D, van Tilbeurgh H, Goris J. Crystal structure of the PP2A phosphatase activator: implications for its PP2A-specific PPIase activity. Mol Cell. 2006 Aug 4;23(3):413-24 This article should be referenced as such: Janssens V. PPP2R4 (protein phosphatase 2A activator, regulatory subunit 4). Atlas Genet Cytogenet Oncol Haematol. 2010; 14(1):48-51. Magnusdottir A, Stenmark P, Flodin S, Nyman T, Hammarström M, Ehn M, Bakali H MA, Berglund H, Nordlund Atlas Genet Cytogenet Oncol Haematol. 2010; 14(1) 51