Literature DB >> 12181365

RNA interference of peroxisome-related genes in C. elegans: a new model for human peroxisomal disorders.

Oleh I Petriv1, David B Pilgrim, Richard A Rachubinski, Vladimir I Titorenko.   

Abstract

RNA-mediated interference (RNAi) for the posttranscriptional silencing of genes was used to evaluate the importance of various peroxisomal enzymes and peroxins for the development of Caenorhabditis elegans and to compare the roles of these proteins in the nematode to their roles in yeasts and humans. The nematode counterparts of the human ATP-binding cassette half-transporters, the enzymes alkyldihydroxyacetonephosphate synthase and Delta(3,5)-Delta (2,4)-dienoyl-CoA isomerase, the receptors for peroxisomal membrane and matrix proteins (Pex19p and Pex5p), and components of the docking and translocation machineries for matrix proteins (Pex13p and Pex12p) are essential for the development of C. elegans. Unexpectedly, RNAi silencing of the acyl-CoA synthetase-mediated activation of fatty acids, the alpha- and beta-oxidation of fatty acids, the intraperoxisomal decomposition of hydrogen peroxide, and the peroxins Pex1p, Pex2p, and Pex6p had no apparent effect on C. elegans development. The described analysis of functional gene knockouts through RNAi provides a basis for the use of C. elegans as a valuable model system with which to study the molecular and physiological defects underlying the human peroxisomal disorders.

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Year:  2002        PMID: 12181365     DOI: 10.1152/physiolgenomics.00044.2002

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  16 in total

Review 1.  Peroxisomal acyl-CoA synthetases.

Authors:  Paul A Watkins; Jessica M Ellis
Journal:  Biochim Biophys Acta       Date:  2012-02-17

Review 2.  Peroxisome deficient invertebrate and vertebrate animal models.

Authors:  Paul P Van Veldhoven; Myriam Baes
Journal:  Front Physiol       Date:  2013-11-22       Impact factor: 4.566

3.  Peroxisomes in zebrafish: distribution pattern and knockdown studies.

Authors:  Olga Krysko; Mieke Stevens; Tobias Langenberg; Marc Fransen; Marc Espeel; Myriam Baes
Journal:  Histochem Cell Biol       Date:  2010-06-17       Impact factor: 4.304

4.  Genetic screen identifies non-mitochondrial proteins involved in the maintenance of mitochondrial homeostasis.

Authors:  Stephane Rolland; Barbara Conradt
Journal:  MicroPubl Biol       Date:  2022-05-11

Review 5.  Genetic-dependency of peroxisomal cell functions - emerging aspects.

Authors:  N Latruffe; J Vamecq; M Cherkaoui Malki
Journal:  J Cell Mol Med       Date:  2003 Jul-Sep       Impact factor: 5.310

6.  Microporation is an efficient method for siRNA-induced knockdown of PEX5 in HepG2 cells: evaluation of the transfection efficiency, the PEX5 mRNA and protein levels and induction of peroxisomal deficiency.

Authors:  Barbara Ahlemeyer; Julia-Franziska Vogt; Vera Michel; Petra Hahn-Kohlberger; Eveline Baumgart-Vogt
Journal:  Histochem Cell Biol       Date:  2014-09-17       Impact factor: 4.304

Review 7.  From peroxisomal disorders to common neurodegenerative diseases - the role of ether phospholipids in the nervous system.

Authors:  Fabian Dorninger; Sonja Forss-Petter; Johannes Berger
Journal:  FEBS Lett       Date:  2017-09-07       Impact factor: 4.124

8.  Integration of peroxisomes into an endomembrane system that governs cellular aging.

Authors:  Adam Beach; Michelle T Burstein; Vincent R Richard; Anna Leonov; Sean Levy; Vladimir I Titorenko
Journal:  Front Physiol       Date:  2012-07-17       Impact factor: 4.566

9.  A Drosophila model for the Zellweger spectrum of peroxisome biogenesis disorders.

Authors:  Fred D Mast; Jing Li; Maninder K Virk; Sarah C Hughes; Andrew J Simmonds; Richard A Rachubinski
Journal:  Dis Model Mech       Date:  2011-06-13       Impact factor: 5.758

10.  The ABC transporter gene family of Daphnia pulex.

Authors:  Armin Sturm; Phil Cunningham; Michael Dean
Journal:  BMC Genomics       Date:  2009-04-21       Impact factor: 3.969

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