Cargando…

A Tether for Woronin Body Inheritance Is Associated with Evolutionary Variation in Organelle Positioning

Eukaryotic organelles evolve to support the lifestyle of evolutionarily related organisms. In the fungi, filamentous Ascomycetes possess dense-core organelles called Woronin bodies (WBs). These organelles originate from peroxisomes and perform an adaptive function to seal septal pores in response to...

Descripción completa

Detalles Bibliográficos
Autores principales: Ng, Seng Kah, Liu, Fangfang, Lai, Julian, Low, Wilson, Jedd, Gregory
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690989/
https://www.ncbi.nlm.nih.gov/pubmed/19543374
http://dx.doi.org/10.1371/journal.pgen.1000521
_version_ 1782167862053437440
author Ng, Seng Kah
Liu, Fangfang
Lai, Julian
Low, Wilson
Jedd, Gregory
author_facet Ng, Seng Kah
Liu, Fangfang
Lai, Julian
Low, Wilson
Jedd, Gregory
author_sort Ng, Seng Kah
collection PubMed
description Eukaryotic organelles evolve to support the lifestyle of evolutionarily related organisms. In the fungi, filamentous Ascomycetes possess dense-core organelles called Woronin bodies (WBs). These organelles originate from peroxisomes and perform an adaptive function to seal septal pores in response to cellular wounding. Here, we identify Leashin, an organellar tether required for WB inheritance, and associate it with evolutionary variation in the subcellular pattern of WB distribution. In Neurospora, the leashin (lah) locus encodes two related adjacent genes. N-terminal sequences of LAH-1 bind WBs via the WB–specific membrane protein WSC, and C-terminal sequences are required for WB inheritance by cell cortex association. LAH-2 is localized to the hyphal apex and septal pore rim and plays a role in colonial growth. In most species, WBs are tethered directly to the pore rim, however, Neurospora and relatives have evolved a delocalized pattern of cortex association. Using a new method for the construction of chromosomally encoded fusion proteins, marker fusion tagging (MFT), we show that a LAH-1/LAH-2 fusion can reproduce the ancestral pattern in Neurospora. Our results identify the link between the WB and cell cortex and suggest that splitting of leashin played a key role in the adaptive evolution of organelle localization.
format Text
id pubmed-2690989
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-26909892009-06-19 A Tether for Woronin Body Inheritance Is Associated with Evolutionary Variation in Organelle Positioning Ng, Seng Kah Liu, Fangfang Lai, Julian Low, Wilson Jedd, Gregory PLoS Genet Research Article Eukaryotic organelles evolve to support the lifestyle of evolutionarily related organisms. In the fungi, filamentous Ascomycetes possess dense-core organelles called Woronin bodies (WBs). These organelles originate from peroxisomes and perform an adaptive function to seal septal pores in response to cellular wounding. Here, we identify Leashin, an organellar tether required for WB inheritance, and associate it with evolutionary variation in the subcellular pattern of WB distribution. In Neurospora, the leashin (lah) locus encodes two related adjacent genes. N-terminal sequences of LAH-1 bind WBs via the WB–specific membrane protein WSC, and C-terminal sequences are required for WB inheritance by cell cortex association. LAH-2 is localized to the hyphal apex and septal pore rim and plays a role in colonial growth. In most species, WBs are tethered directly to the pore rim, however, Neurospora and relatives have evolved a delocalized pattern of cortex association. Using a new method for the construction of chromosomally encoded fusion proteins, marker fusion tagging (MFT), we show that a LAH-1/LAH-2 fusion can reproduce the ancestral pattern in Neurospora. Our results identify the link between the WB and cell cortex and suggest that splitting of leashin played a key role in the adaptive evolution of organelle localization. Public Library of Science 2009-06-19 /pmc/articles/PMC2690989/ /pubmed/19543374 http://dx.doi.org/10.1371/journal.pgen.1000521 Text en Ng et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ng, Seng Kah
Liu, Fangfang
Lai, Julian
Low, Wilson
Jedd, Gregory
A Tether for Woronin Body Inheritance Is Associated with Evolutionary Variation in Organelle Positioning
title A Tether for Woronin Body Inheritance Is Associated with Evolutionary Variation in Organelle Positioning
title_full A Tether for Woronin Body Inheritance Is Associated with Evolutionary Variation in Organelle Positioning
title_fullStr A Tether for Woronin Body Inheritance Is Associated with Evolutionary Variation in Organelle Positioning
title_full_unstemmed A Tether for Woronin Body Inheritance Is Associated with Evolutionary Variation in Organelle Positioning
title_short A Tether for Woronin Body Inheritance Is Associated with Evolutionary Variation in Organelle Positioning
title_sort tether for woronin body inheritance is associated with evolutionary variation in organelle positioning
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690989/
https://www.ncbi.nlm.nih.gov/pubmed/19543374
http://dx.doi.org/10.1371/journal.pgen.1000521
work_keys_str_mv AT ngsengkah atetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning
AT liufangfang atetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning
AT laijulian atetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning
AT lowwilson atetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning
AT jeddgregory atetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning
AT ngsengkah tetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning
AT liufangfang tetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning
AT laijulian tetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning
AT lowwilson tetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning
AT jeddgregory tetherforworoninbodyinheritanceisassociatedwithevolutionaryvariationinorganellepositioning