Literature DB >> 33112423

The Saccharomyces cerevisiae ABC subfamily D transporter Pxa1/Pxa2p co-imports CoASH into the peroxisome.

Carlo W T van Roermund1, Lodewijk IJlst1, Alison Baker2, Ronald J A Wanders1, Freddie L Theodoulou3, Hans R Waterham1.   

Abstract

ATP-binding cassette (ABC) subfamily D transporters are important for the uptake of fatty acids and other beta-oxidation substrates into peroxisomes. Genetic and biochemical evidence indicates that the transporters accept fatty acyl-coenzyme A that is cleaved during the transport cycle and then re-esterified in the peroxisomal lumen. However, it is not known whether free coenzyme A (CoA) is released inside or outside the peroxisome. Here we have used Saccharomyces cerevisiae and isolated peroxisomes to demonstrate that free CoA is released in the peroxisomal lumen. Thus, ABC subfamily D transporter provide an import pathway for free CoA that controls peroxisomal CoA homeostasis and tunes metabolism according to the cell's demands.
© 2020 Federation of European Biochemical Societies.

Entities:  

Keywords:  ABC transporter; acyl-CoA; coenzyme A; coenzyme homeostasis; peroxisome; thioesterase

Year:  2020        PMID: 33112423     DOI: 10.1002/1873-3468.13974

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  4 in total

Review 1.  Peroxisomal ABC Transporters: An Update.

Authors:  Ali Tawbeh; Catherine Gondcaille; Doriane Trompier; Stéphane Savary
Journal:  Int J Mol Sci       Date:  2021-06-05       Impact factor: 5.923

2.  Peroxisomal ATP Uptake Is Provided by Two Adenine Nucleotide Transporters and the ABCD Transporters.

Authors:  Carlo W T van Roermund; Lodewijk IJlst; Nicole Linka; Ronald J A Wanders; Hans R Waterham
Journal:  Front Cell Dev Biol       Date:  2022-01-19

3.  Systematic multi-level analysis of an organelle proteome reveals new peroxisomal functions.

Authors:  Eden Yifrach; Duncan Holbrook-Smith; Jérôme Bürgi; Alaa Othman; Miriam Eisenstein; Carlo Wt van Roermund; Wouter Visser; Asa Tirosh; Markus Rudowitz; Chen Bibi; Shahar Galor; Uri Weill; Amir Fadel; Yoav Peleg; Ralf Erdmann; Hans R Waterham; Ronald J A Wanders; Matthias Wilmanns; Nicola Zamboni; Maya Schuldiner; Einat Zalckvar
Journal:  Mol Syst Biol       Date:  2022-09       Impact factor: 13.068

4.  Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis.

Authors:  Pablo Ranea-Robles; Sara Violante; Carmen Argmann; Tetyana Dodatko; Dipankar Bhattacharya; Hongjie Chen; Chunli Yu; Scott L Friedman; Michelle Puchowicz; Sander M Houten
Journal:  Cell Mol Life Sci       Date:  2021-06-10       Impact factor: 9.207

  4 in total

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