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Msh4 and Msh5 Function in SC-Independent Chiasma Formation During the Streamlined Meiosis of Tetrahymena

ZMM proteins have been defined in budding yeast as factors that are collectively involved in the formation of interfering crossovers (COs) and synaptonemal complexes (SCs), and they are a hallmark of the predominant meiotic recombination pathway of most organisms. In addition to this so-called class...

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Autores principales: Shodhan, Anura, Lukaszewicz, Agnieszka, Novatchkova, Maria, Loidl, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224184/
https://www.ncbi.nlm.nih.gov/pubmed/25217051
http://dx.doi.org/10.1534/genetics.114.169698
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author Shodhan, Anura
Lukaszewicz, Agnieszka
Novatchkova, Maria
Loidl, Josef
author_facet Shodhan, Anura
Lukaszewicz, Agnieszka
Novatchkova, Maria
Loidl, Josef
author_sort Shodhan, Anura
collection PubMed
description ZMM proteins have been defined in budding yeast as factors that are collectively involved in the formation of interfering crossovers (COs) and synaptonemal complexes (SCs), and they are a hallmark of the predominant meiotic recombination pathway of most organisms. In addition to this so-called class I CO pathway, a minority of crossovers are formed by a class II pathway, which involves the Mus81-Mms4 endonuclease complex. This is the only CO pathway in the SC-less meiosis of the fission yeast. ZMM proteins (including SC components) were always found to be co-occurring and hence have been regarded as functionally linked. Like the fission yeast, the protist Tetrahymena thermophila does not possess a SC, and its COs are dependent on Mus81-Mms4. Here we show that the ZMM proteins Msh4 and Msh5 are required for normal chiasma formation, and we propose that they have a pro-CO function outside a canonical class I pathway in Tetrahymena. Thus, the two-pathway model is not tenable as a general rule.
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spelling pubmed-42241842014-11-10 Msh4 and Msh5 Function in SC-Independent Chiasma Formation During the Streamlined Meiosis of Tetrahymena Shodhan, Anura Lukaszewicz, Agnieszka Novatchkova, Maria Loidl, Josef Genetics Investigations ZMM proteins have been defined in budding yeast as factors that are collectively involved in the formation of interfering crossovers (COs) and synaptonemal complexes (SCs), and they are a hallmark of the predominant meiotic recombination pathway of most organisms. In addition to this so-called class I CO pathway, a minority of crossovers are formed by a class II pathway, which involves the Mus81-Mms4 endonuclease complex. This is the only CO pathway in the SC-less meiosis of the fission yeast. ZMM proteins (including SC components) were always found to be co-occurring and hence have been regarded as functionally linked. Like the fission yeast, the protist Tetrahymena thermophila does not possess a SC, and its COs are dependent on Mus81-Mms4. Here we show that the ZMM proteins Msh4 and Msh5 are required for normal chiasma formation, and we propose that they have a pro-CO function outside a canonical class I pathway in Tetrahymena. Thus, the two-pathway model is not tenable as a general rule. Genetics Society of America 2014-11 2014-09-11 /pmc/articles/PMC4224184/ /pubmed/25217051 http://dx.doi.org/10.1534/genetics.114.169698 Text en Copyright © 2014 by the Genetics Society of America Available freely online through the author-supported open access option.
spellingShingle Investigations
Shodhan, Anura
Lukaszewicz, Agnieszka
Novatchkova, Maria
Loidl, Josef
Msh4 and Msh5 Function in SC-Independent Chiasma Formation During the Streamlined Meiosis of Tetrahymena
title Msh4 and Msh5 Function in SC-Independent Chiasma Formation During the Streamlined Meiosis of Tetrahymena
title_full Msh4 and Msh5 Function in SC-Independent Chiasma Formation During the Streamlined Meiosis of Tetrahymena
title_fullStr Msh4 and Msh5 Function in SC-Independent Chiasma Formation During the Streamlined Meiosis of Tetrahymena
title_full_unstemmed Msh4 and Msh5 Function in SC-Independent Chiasma Formation During the Streamlined Meiosis of Tetrahymena
title_short Msh4 and Msh5 Function in SC-Independent Chiasma Formation During the Streamlined Meiosis of Tetrahymena
title_sort msh4 and msh5 function in sc-independent chiasma formation during the streamlined meiosis of tetrahymena
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224184/
https://www.ncbi.nlm.nih.gov/pubmed/25217051
http://dx.doi.org/10.1534/genetics.114.169698
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