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...
Gespeichert in:
Veröffentlicht in: | Biochimica et biophysica acta. Molecular cell research 2018-04, Vol.1865 (4), p.572-586 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 586 |
---|---|
container_issue | 4 |
container_start_page | 572 |
container_title | Biochimica et biophysica acta. Molecular cell research |
container_volume | 1865 |
creator | Suaste-Olmos, Fernando 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. |
doi_str_mv | 10.1016/j.bbamcr.2018.01.003 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1989559152</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S016748891830003X</els_id><sourcerecordid>1989559152</sourcerecordid><originalsourceid>FETCH-LOGICAL-c362t-d51efc6799e56a0439d073232e3bdfeab19e0701b9d7fa4b82b84bd6a00f24193</originalsourceid><addsrcrecordid>eNp9kE1PHSEUhklTo1frPzCGZTczBeaDYWPSGKtNbHRh14SPM5WbOzAXGOP99-V6tcueDSfkeXnDg9AFJTUltP-2rrVWk4k1I3SoCa0JaT6hFR24qFgn-s9oVTBetcMgTtBpSmtSpuXdMTphoiGcD90KbX-BC9kZbOEFNmGewGfsvMtOZRd8WXF-Bjwu_s-S8GOwIc0hKqx8gui8whG2i4uQ3rAZYnh1KUxQ7g3MOUQMryWQ8aTMs_MQd1_Q0ag2Cc7fzzP0-8fN0_Vddf9w-_P6-31lmp7lynYURtNzIaDrFWkbYQlvWMOg0XYEpakAwgnVwvJRtXpgemi1LSgZWUtFc4a-Ht6dY9gukLKcXDKw2SgPYUmSikF0naAdK2h7QE0MKUUY5RzdpOJOUiL3suVaHmTLvWxJqCyyS-zyvWHRE9h_oQ-7Bbg6AFD--eIgymQceAO2GDNZ2uD-3_AXpcmVHQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1989559152</pqid></control><display><type>article</type><title>Meiotic development initiation in the fungus Podospora anserina requires the peroxisome receptor export machinery</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Suaste-Olmos, Fernando ; Zirión-Martínez, Claudia ; Takano-Rojas, Harumi ; Peraza-Reyes, Leonardo</creator><creatorcontrib>Suaste-Olmos, Fernando ; Zirión-Martínez, Claudia ; Takano-Rojas, Harumi ; Peraza-Reyes, Leonardo</creatorcontrib><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.</description><identifier>ISSN: 0167-4889</identifier><identifier>EISSN: 1879-2596</identifier><identifier>DOI: 10.1016/j.bbamcr.2018.01.003</identifier><identifier>PMID: 29307785</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>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</subject><ispartof>Biochimica et biophysica acta. Molecular cell research, 2018-04, Vol.1865 (4), p.572-586</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-d51efc6799e56a0439d073232e3bdfeab19e0701b9d7fa4b82b84bd6a00f24193</citedby><cites>FETCH-LOGICAL-c362t-d51efc6799e56a0439d073232e3bdfeab19e0701b9d7fa4b82b84bd6a00f24193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S016748891830003X$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29307785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suaste-Olmos, Fernando</creatorcontrib><creatorcontrib>Zirión-Martínez, Claudia</creatorcontrib><creatorcontrib>Takano-Rojas, Harumi</creatorcontrib><creatorcontrib>Peraza-Reyes, Leonardo</creatorcontrib><title>Meiotic development initiation in the fungus Podospora anserina requires the peroxisome receptor export machinery</title><title>Biochimica et biophysica acta. Molecular cell research</title><addtitle>Biochim Biophys Acta Mol Cell Res</addtitle><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.</description><subject>Cysteine - metabolism</subject><subject>Fatty Acids - metabolism</subject><subject>Fungal Proteins - metabolism</subject><subject>Fungi</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Meiosis</subject><subject>Models, Biological</subject><subject>Mycelium - metabolism</subject><subject>Organelle biogenesis</subject><subject>Peroxisome</subject><subject>Peroxisomes - metabolism</subject><subject>Podospora - cytology</subject><subject>Podospora - metabolism</subject><subject>Protein Transport</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Sexual development</subject><subject>Ubiquitination</subject><issn>0167-4889</issn><issn>1879-2596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1PHSEUhklTo1frPzCGZTczBeaDYWPSGKtNbHRh14SPM5WbOzAXGOP99-V6tcueDSfkeXnDg9AFJTUltP-2rrVWk4k1I3SoCa0JaT6hFR24qFgn-s9oVTBetcMgTtBpSmtSpuXdMTphoiGcD90KbX-BC9kZbOEFNmGewGfsvMtOZRd8WXF-Bjwu_s-S8GOwIc0hKqx8gui8whG2i4uQ3rAZYnh1KUxQ7g3MOUQMryWQ8aTMs_MQd1_Q0ag2Cc7fzzP0-8fN0_Vddf9w-_P6-31lmp7lynYURtNzIaDrFWkbYQlvWMOg0XYEpakAwgnVwvJRtXpgemi1LSgZWUtFc4a-Ht6dY9gukLKcXDKw2SgPYUmSikF0naAdK2h7QE0MKUUY5RzdpOJOUiL3suVaHmTLvWxJqCyyS-zyvWHRE9h_oQ-7Bbg6AFD--eIgymQceAO2GDNZ2uD-3_AXpcmVHQ</recordid><startdate>201804</startdate><enddate>201804</enddate><creator>Suaste-Olmos, Fernando</creator><creator>Zirión-Martínez, Claudia</creator><creator>Takano-Rojas, Harumi</creator><creator>Peraza-Reyes, Leonardo</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201804</creationdate><title>Meiotic development initiation in the fungus Podospora anserina requires the peroxisome receptor export machinery</title><author>Suaste-Olmos, Fernando ; Zirión-Martínez, Claudia ; Takano-Rojas, Harumi ; Peraza-Reyes, Leonardo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-d51efc6799e56a0439d073232e3bdfeab19e0701b9d7fa4b82b84bd6a00f24193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Cysteine - metabolism</topic><topic>Fatty Acids - metabolism</topic><topic>Fungal Proteins - metabolism</topic><topic>Fungi</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Meiosis</topic><topic>Models, Biological</topic><topic>Mycelium - metabolism</topic><topic>Organelle biogenesis</topic><topic>Peroxisome</topic><topic>Peroxisomes - metabolism</topic><topic>Podospora - cytology</topic><topic>Podospora - metabolism</topic><topic>Protein Transport</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>Sexual development</topic><topic>Ubiquitination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suaste-Olmos, Fernando</creatorcontrib><creatorcontrib>Zirión-Martínez, Claudia</creatorcontrib><creatorcontrib>Takano-Rojas, Harumi</creatorcontrib><creatorcontrib>Peraza-Reyes, Leonardo</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochimica et biophysica acta. Molecular cell research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suaste-Olmos, Fernando</au><au>Zirión-Martínez, Claudia</au><au>Takano-Rojas, Harumi</au><au>Peraza-Reyes, Leonardo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Meiotic development initiation in the fungus Podospora anserina requires the peroxisome receptor export machinery</atitle><jtitle>Biochimica et biophysica acta. Molecular cell research</jtitle><addtitle>Biochim Biophys Acta Mol Cell Res</addtitle><date>2018-04</date><risdate>2018</risdate><volume>1865</volume><issue>4</issue><spage>572</spage><epage>586</epage><pages>572-586</pages><issn>0167-4889</issn><eissn>1879-2596</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 0167-4889 |
ispartof | Biochimica et biophysica acta. Molecular cell research, 2018-04, Vol.1865 (4), p.572-586 |
issn | 0167-4889 1879-2596 |
language | eng |
recordid | cdi_proquest_miscellaneous_1989559152 |
source | MEDLINE; Elsevier ScienceDirect Journals; EZB-FREE-00999 freely available EZB journals |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T00%3A26%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Meiotic%20development%20initiation%20in%20the%20fungus%20Podospora%20anserina%20requires%20the%20peroxisome%20receptor%20export%20machinery&rft.jtitle=Biochimica%20et%20biophysica%20acta.%20Molecular%20cell%20research&rft.au=Suaste-Olmos,%20Fernando&rft.date=2018-04&rft.volume=1865&rft.issue=4&rft.spage=572&rft.epage=586&rft.pages=572-586&rft.issn=0167-4889&rft.eissn=1879-2596&rft_id=info:doi/10.1016/j.bbamcr.2018.01.003&rft_dat=%3Cproquest_cross%3E1989559152%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1989559152&rft_id=info:pmid/29307785&rft_els_id=S016748891830003X&rfr_iscdi=true |