Literature DB >> 20964547

Is overoxidation of peroxiredoxin physiologically significant?

Maike Thamsen1, Caroline Kumsta, Fei Li, Ursula Jakob.   

Abstract

Eukaryotic peroxiredoxins are highly susceptible to sulfinic acid formation. This overoxidation, which is thought to convert peroxiredoxins into chaperones, can be reversed by sulfiredoxins. Several organisms, including Caenorhabditis elegans, lack sulfiredoxins but encode sestrins, proteins proposed to be functionally equivalent. We induced peroxiredoxin overoxidation in C. elegans with a short peroxide pulse. We found that reduction of overoxidized peroxiredoxin 2 (PRDX-2) was extremely slow and sestrin-independent, strongly implying that worms lack an efficient repair system. Analysis of PRDX-2's overoxidation status during C. elegans lifespan revealed no accumulation of overoxidized PRDX-2 at any point, questioning whether PRDX-2 overoxidation in worms is physiologically relevant.

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Year:  2010        PMID: 20964547      PMCID: PMC3021361          DOI: 10.1089/ars.2010.3717

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  27 in total

1.  Reversing the inactivation of peroxiredoxins caused by cysteine sulfinic acid formation.

Authors:  Hyun Ae Woo; Ho Zoon Chae; Sung Chul Hwang; Kap-Seok Yang; Sang Won Kang; Kanghwa Kim; Sue Goo Rhee
Journal:  Science       Date:  2003-04-25       Impact factor: 47.728

2.  The aging process of the nematode Caenorhabditis elegans in bacterial and axenic culture.

Authors:  N A Croll; J M Smith; B M Zuckerman
Journal:  Exp Aging Res       Date:  1977-05       Impact factor: 1.645

Review 3.  Reduction of cysteine sulfinic acid in eukaryotic, typical 2-Cys peroxiredoxins by sulfiredoxin.

Authors:  W Todd Lowther; Alexina C Haynes
Journal:  Antioxid Redox Signal       Date:  2010-12-17       Impact factor: 8.401

4.  Inactivation of human peroxiredoxin I during catalysis as the result of the oxidation of the catalytic site cysteine to cysteine-sulfinic acid.

Authors:  Kap-Seok Yang; Sang Won Kang; Hyun Ae Woo; Sung Chul Hwang; Ho Zoon Chae; Kanghwa Kim; Sue Goo Rhee
Journal:  J Biol Chem       Date:  2002-08-02       Impact factor: 5.157

5.  Regeneration of peroxiredoxins by p53-regulated sestrins, homologs of bacterial AhpD.

Authors:  Andrei V Budanov; Anna A Sablina; Elena Feinstein; Eugene V Koonin; Peter M Chumakov
Journal:  Science       Date:  2004-04-23       Impact factor: 47.728

Review 6.  Oxidative DNA damage and disease: induction, repair and significance.

Authors:  Mark D Evans; Miral Dizdaroglu; Marcus S Cooke
Journal:  Mutat Res       Date:  2004-09       Impact factor: 2.433

7.  Essential role for the peroxiredoxin Prdx1 in erythrocyte antioxidant defence and tumour suppression.

Authors:  Carola A Neumann; Daniela S Krause; Christopher V Carman; Shampa Das; Devendra P Dubey; Jennifer L Abraham; Roderick T Bronson; Yuko Fujiwara; Stuart H Orkin; Richard A Van Etten
Journal:  Nature       Date:  2003-07-31       Impact factor: 49.962

8.  A peroxiredoxin specifically expressed in two types of pharyngeal neurons is required for normal growth and egg production in Caenorhabditis elegans.

Authors:  Kerstin Isermann; Eva Liebau; Thomas Roeder; Iris Bruchhaus
Journal:  J Mol Biol       Date:  2004-05-07       Impact factor: 5.469

9.  ATP-dependent reduction of cysteine-sulphinic acid by S. cerevisiae sulphiredoxin.

Authors:  Benoît Biteau; Jean Labarre; Michel B Toledano
Journal:  Nature       Date:  2003-10-30       Impact factor: 49.962

10.  Two enzymes in one; two yeast peroxiredoxins display oxidative stress-dependent switching from a peroxidase to a molecular chaperone function.

Authors:  Ho Hee Jang; Kyun Oh Lee; Yong Hun Chi; Bae Gyo Jung; Soo Kwon Park; Jin Ho Park; Jung Ro Lee; Seung Sik Lee; Jeong Chan Moon; Jeong Won Yun; Yeon Ok Choi; Woe Yeon Kim; Ji Seoun Kang; Gang-Won Cheong; Dae-Jin Yun; Sue Goo Rhee; Moo Je Cho; Sang Yeol Lee
Journal:  Cell       Date:  2004-05-28       Impact factor: 41.582

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  18 in total

Review 1.  Peroxiredoxins in parasites.

Authors:  Michael C Gretes; Leslie B Poole; P Andrew Karplus
Journal:  Antioxid Redox Signal       Date:  2012-01-25       Impact factor: 8.401

Review 2.  The Multifaceted Impact of Peroxiredoxins on Aging and Disease.

Authors:  Svetlana N Radyuk; William C Orr
Journal:  Antioxid Redox Signal       Date:  2018-01-17       Impact factor: 8.401

Review 3.  Biochemical Basis of Sestrin Physiological Activities.

Authors:  Allison Ho; Chun-Seok Cho; Sim Namkoong; Uhn-Soo Cho; Jun Hee Lee
Journal:  Trends Biochem Sci       Date:  2016-05-10       Impact factor: 13.807

Review 4.  Maintaining a Healthy Proteome during Oxidative Stress.

Authors:  Dana Reichmann; Wilhelm Voth; Ursula Jakob
Journal:  Mol Cell       Date:  2018-01-18       Impact factor: 17.970

5.  The role of sulfenic acids in cellular redox signaling: Reconciling chemical kinetics and molecular detection strategies.

Authors:  David E Heppner; Yvonne M W Janssen-Heininger; Albert van der Vliet
Journal:  Arch Biochem Biophys       Date:  2017-01-23       Impact factor: 4.013

Review 6.  Role of reactive oxygen species-mediated signaling in aging.

Authors:  Vyacheslav M Labunskyy; Vadim N Gladyshev
Journal:  Antioxid Redox Signal       Date:  2012-09-20       Impact factor: 8.401

Review 7.  Peroxiredoxins, gerontogenes linking aging to genome instability and cancer.

Authors:  Thomas Nyström; Junsheng Yang; Mikael Molin
Journal:  Genes Dev       Date:  2012-09-15       Impact factor: 11.361

8.  The Interplay Between Peroxiredoxin-2 and Nuclear Factor-Erythroid 2 Is Important in Limiting Oxidative Mediated Dysfunction in β-Thalassemic Erythropoiesis.

Authors:  Alessandro Matte; Luigia De Falco; Achille Iolascon; Narla Mohandas; Xiuli An; Angela Siciliano; Christophe Leboeuf; Anne Janin; Mariasole Bruno; Soo Young Choi; Dae Won Kim; Lucia De Franceschi
Journal:  Antioxid Redox Signal       Date:  2015-07-14       Impact factor: 8.401

9.  Metformin promotes lifespan through mitohormesis via the peroxiredoxin PRDX-2.

Authors:  Wouter De Haes; Lotte Frooninckx; Roel Van Assche; Arne Smolders; Geert Depuydt; Johan Billen; Bart P Braeckman; Liliane Schoofs; Liesbet Temmerman
Journal:  Proc Natl Acad Sci U S A       Date:  2014-06-02       Impact factor: 11.205

10.  Sestrin2 decreases renal oxidative stress, lowers blood pressure, and mediates dopamine D2 receptor-induced inhibition of reactive oxygen species production.

Authors:  Yu Yang; Santiago Cuevas; Sufei Yang; Van Anthony Villar; Crisanto Escano; Laureano Asico; Peiying Yu; Xiaoliang Jiang; Edward J Weinman; Ines Armando; Pedro A Jose
Journal:  Hypertension       Date:  2014-07-14       Impact factor: 10.190

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