Meiotic development initiation in the fungus Podospora anserina requires the peroxisome receptor export machinery

Peroxisomes are versatile organelles essential for diverse developmental processes. One such process is the meiotic development of Podospora anserina. In this fungus, absence of the docking peroxin PEX13, the RING-finger complex peroxins, or the PTS2 co-receptor PEX20 blocks sexual development befor...

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Veröffentlicht in:Biochimica et biophysica acta. Molecular cell research 2018-04, Vol.1865 (4), p.572-586
Hauptverfasser: Suaste-Olmos, Fernando, Zirión-Martínez, Claudia, Takano-Rojas, Harumi, Peraza-Reyes, Leonardo
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container_title Biochimica et biophysica acta. Molecular cell research
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Zirión-Martínez, Claudia
Takano-Rojas, Harumi
Peraza-Reyes, Leonardo
description Peroxisomes are versatile organelles essential for diverse developmental processes. One such process is the meiotic development of Podospora anserina. In this fungus, absence of the docking peroxin PEX13, the RING-finger complex peroxins, or the PTS2 co-receptor PEX20 blocks sexual development before meiocyte formation. However, this defect is not seen in the absence of the receptors PEX5 and PEX7, or of the docking peroxins PEX14 and PEX14/17. Here we describe the function of the remaining uncharacterized P. anserina peroxins predictably involved in peroxisome matrix protein import. We show that PEX8, as well as the peroxins potentially mediating receptor monoubiquitination (PEX4 and PEX22) and membrane dislocation (PEX1, PEX6 and PEX26) are indeed implicated in peroxisome matrix protein import in this fungus. However, we observed that elimination of PEX4 and PEX22 affects to different extent the import of distinct PEX5 cargoes, suggesting differential ubiquitination-complex requirements for the import of distinct proteins. In addition, we found that elimination of PEX1, PEX6 or PEX26 results in loss of peroxisomes, suggesting that these peroxins restrain peroxisome removal in specific physiological conditions. Finally, we demonstrate that all analyzed peroxins are required for meiocyte formation, and that PEX20 function in this process depends on its potential monoubiquitination target cysteine. Our results suggest that meiotic induction relies on a peroxisome import pathway, which is not dependent on PEX5 or PEX7 but that is driven by an additional cycling receptor. These findings uncover a collection of peroxins implicated in modulating peroxisome activity to facilitate a critical developmental cell fate decision. [Display omitted] •P. anserina peroxisomes differ in their protein composition and distribution.•The import of distinct proteins differs in its ubiquitination-complex requirements.•The peroxisome dislocation complex restrains peroxisome removal in P. anserina.•Meiotic induction in P. anserina requires PEX8 and the exportomer peroxins.•Meiotic induction requires the PEX20 cysteine that is potentially monoubiquitinated.
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In this fungus, absence of the docking peroxin PEX13, the RING-finger complex peroxins, or the PTS2 co-receptor PEX20 blocks sexual development before meiocyte formation. However, this defect is not seen in the absence of the receptors PEX5 and PEX7, or of the docking peroxins PEX14 and PEX14/17. Here we describe the function of the remaining uncharacterized P. anserina peroxins predictably involved in peroxisome matrix protein import. We show that PEX8, as well as the peroxins potentially mediating receptor monoubiquitination (PEX4 and PEX22) and membrane dislocation (PEX1, PEX6 and PEX26) are indeed implicated in peroxisome matrix protein import in this fungus. However, we observed that elimination of PEX4 and PEX22 affects to different extent the import of distinct PEX5 cargoes, suggesting differential ubiquitination-complex requirements for the import of distinct proteins. In addition, we found that elimination of PEX1, PEX6 or PEX26 results in loss of peroxisomes, suggesting that these peroxins restrain peroxisome removal in specific physiological conditions. Finally, we demonstrate that all analyzed peroxins are required for meiocyte formation, and that PEX20 function in this process depends on its potential monoubiquitination target cysteine. Our results suggest that meiotic induction relies on a peroxisome import pathway, which is not dependent on PEX5 or PEX7 but that is driven by an additional cycling receptor. These findings uncover a collection of peroxins implicated in modulating peroxisome activity to facilitate a critical developmental cell fate decision. [Display omitted] •P. anserina peroxisomes differ in their protein composition and distribution.•The import of distinct proteins differs in its ubiquitination-complex requirements.•The peroxisome dislocation complex restrains peroxisome removal in P. anserina.•Meiotic induction in P. anserina requires PEX8 and the exportomer peroxins.•Meiotic induction requires the PEX20 cysteine that is potentially monoubiquitinated.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29307785</pmid><doi>10.1016/j.bbamcr.2018.01.003</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record>
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subjects Cysteine - metabolism
Fatty Acids - metabolism
Fungal Proteins - metabolism
Fungi
Green Fluorescent Proteins - metabolism
Meiosis
Models, Biological
Mycelium - metabolism
Organelle biogenesis
Peroxisome
Peroxisomes - metabolism
Podospora - cytology
Podospora - metabolism
Protein Transport
Receptors, Cell Surface - metabolism
Recombinant Fusion Proteins - metabolism
Sexual development
Ubiquitination
title Meiotic development initiation in the fungus Podospora anserina requires the peroxisome receptor export machinery
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