Difference between revisions of "Phosphatase Subfamily Acr2"

Revision as of 17:16, 27 May 2014

Phosphatase Classification: Superfamily Cys-based II: Family CDC25: Subfamily Acr2

Prokaryotes and eukaryotes use arsenate reductases of distinct folds. E. coli uses ArsC, which belongs to Superfamily Cys-based III, the same as LMWPTP and SSU72. Eukaryotes, particularly fungi, plants and protists, may use ACR2 which have the same fold as CDC25 [1]. However, knocking out ACR2 does not affect arsenic redox status in Arabidopsis thaliana and Saccharomyces cerevisiae , which implies the existence of other arsenate reductase(s) in plants and yeast [2].

Arc2 in eukaryotes

Saccharomyces cerevisiae. Overexpressed in E. coli, ARR2, the ACR2 gene of Saccharomyces cerevisiae, was shown to exhibit arsenate reductase activity and complement the arsenate-sensitive phenotype of an ArsC deletion in E. coli [1, 3, 4]. The Cx5R motif is required for its catalytic activity as arsenate reductase [5].

Arabidopsis thaliana. Acr2 of Arabidopsis thaliana was initially characterized as a phosphatase, given the evidences: i) protein structure solved by NMR [6], ii) recombinant expression in E. coli shows tyrosine phosphatase activity towards artificial substrate [7], and iii) overexpression in fission yeast function suggests it is a mitotic accelerator [8]. It has been suggested to play a role in arsenate reduction [9, 10, 11]. However, knocking out ACR2 does not affect arsenic redox status in Arabidopsis thaliana and Saccharomyces cerevisiae [2].

Pteris vittata (fern). The ACR2 of "Pteris vittata" (PvACR2) can suppress the arsenate sensitivity and arsenic hyperaccumulation phenotypes of yeast (Saccharomyces cerevisiae) lacking the arsenate reductase gene ACR2 [11, 12]. However, PvACR2 is unique in that the arginine of catalytic motif Cx5R, previously shown to be essential for phosphatase and reductase activity, is replaced with a serine.

Chlamydomonas reinhardtii (green alga). Chlamydomonas reinhardtii has two Acr2s. One of them complement the arsenate-sensitive phenotype of an ArsC deletion in E. coli [13]

Reference

1. Yeo HK and Lee JY. Crystal structure of Saccharomyces cerevisiae Ygr203w, a homolog of single-domain rhodanese and Cdc25 phosphatase catalytic domain. Proteins. 2009 Aug 1;76(2):520-4. DOI:10.1002/prot.22420 | PubMed ID:19382206 | HubMed [yeo09]
2. Liu W, Schat H, Bliek M, Chen Y, McGrath SP, George G, Salt DE, and Zhao FJ. Knocking out ACR2 does not affect arsenic redox status in Arabidopsis thaliana: implications for as detoxification and accumulation in plants. PLoS One. 2012;7(8):e42408. DOI:10.1371/journal.pone.0042408 | PubMed ID:22879969 | HubMed [atha-ar-12]
3. Mukhopadhyay R and Rosen BP. Saccharomyces cerevisiae ACR2 gene encodes an arsenate reductase. FEMS Microbiol Lett. 1998 Nov 1;168(1):127-36. DOI:10.1111/j.1574-6968.1998.tb13265.x | PubMed ID:9812373 | HubMed [yeast98]
4. Mukhopadhyay R, Shi J, and Rosen BP. Purification and characterization of ACR2p, the Saccharomyces cerevisiae arsenate reductase. J Biol Chem. 2000 Jul 14;275(28):21149-57. DOI:10.1074/jbc.M910401199 | PubMed ID:10801893 | HubMed [yeast00]
5. Mukhopadhyay R and Rosen BP. The phosphatase C(X)5R motif is required for catalytic activity of the Saccharomyces cerevisiae Acr2p arsenate reductase. J Biol Chem. 2001 Sep 14;276(37):34738-42. DOI:10.1074/jbc.M103354200 | PubMed ID:11461905 | HubMed [yeast01]
6. Landrieu I, da Costa M, De Veylder L, Dewitte F, Vandepoele K, Hassan S, Wieruszeski JM, Corellou F, Faure JD, Van Montagu M, Inzé D, and Lippens G. A small CDC25 dual-specificity tyrosine-phosphatase isoform in Arabidopsis thaliana. Proc Natl Acad Sci U S A. 2004 Sep 7;101(36):13380-5. DOI:10.1073/pnas.0405248101 | PubMed ID:15329414 | HubMed [atha-phosphatase-04]
7. Landrieu I, da Costa M, De Veylder L, Dewitte F, Vandepoele K, Hassan S, Wieruszeski JM, Corellou F, Faure JD, Van Montagu M, Inzé D, and Lippens G. A small CDC25 dual-specificity tyrosine-phosphatase isoform in Arabidopsis thaliana. Proc Natl Acad Sci U S A. 2004 Sep 7;101(36):13380-5. DOI:10.1073/pnas.0405248101 | PubMed ID:15329414 | HubMed [atha-phosphatase-04b]
8. Sorrell DA, Chrimes D, Dickinson JR, Rogers HJ, and Francis D. The Arabidopsis CDC25 induces a short cell length when overexpressed in fission yeast: evidence for cell cycle function. New Phytol. 2005 Feb;165(2):425-8. DOI:10.1111/j.1469-8137.2004.01288.x | PubMed ID:15720653 | HubMed [atha-phosphatase-05]
9. Bleeker PM, Hakvoort HW, Bliek M, Souer E, and Schat H. Enhanced arsenate reduction by a CDC25-like tyrosine phosphatase explains increased phytochelatin accumulation in arsenate-tolerant Holcus lanatus. Plant J. 2006 Mar;45(6):917-29. DOI:10.1111/j.1365-313X.2005.02651.x | PubMed ID:16507083 | HubMed [atha-ar-06]
10. Dhankher OP, Rosen BP, McKinney EC, and Meagher RB. Hyperaccumulation of arsenic in the shoots of Arabidopsis silenced for arsenate reductase (ACR2). Proc Natl Acad Sci U S A. 2006 Apr 4;103(14):5413-8. DOI:10.1073/pnas.0509770102 | PubMed ID:16567632 | HubMed [atha-ar-06b]
11. Duan GL, Zhu YG, Tong YP, Cai C, and Kneer R. Characterization of arsenate reductase in the extract of roots and fronds of Chinese brake fern, an arsenic hyperaccumulator. Plant Physiol. 2005 May;138(1):461-9. DOI:10.1104/pp.104.057422 | PubMed ID:15834011 | HubMed [fern05]
12. Ellis DR, Gumaelius L, Indriolo E, Pickering IJ, Banks JA, and Salt DE. A novel arsenate reductase from the arsenic hyperaccumulating fern Pteris vittata. Plant Physiol. 2006 Aug;141(4):1544-54. DOI:10.1104/pp.106.084079 | PubMed ID:16766666 | HubMed [fern06]
13. Yin X, Wang L, Duan G, and Sun G. Characterization of arsenate transformation and identification of arsenate reductase in a green alga Chlamydomonas reinhardtii. J Environ Sci (China). 2011;23(7):1186-93. DOI:10.1016/s1001-0742(10)60492-5 | PubMed ID:22125913 | HubMed [green-alga-11]