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Cuf2 Is a Novel Meiosis-Specific Regulatory Factor of Meiosis Maturation
BACKGROUND: Meiosis is the specialized form of the cell cycle by which diploid cells produce the haploid gametes required for sexual reproduction. Initiation and progression through meiosis requires that the expression of the meiotic genes is precisely controlled so as to provide the correct gene pr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338643/ https://www.ncbi.nlm.nih.gov/pubmed/22558440 http://dx.doi.org/10.1371/journal.pone.0036338 |
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author | Ioannoni, Raphael Beaudoin, Jude Lopez-Maury, Luis Codlin, Sandra Bahler, Jurg Labbe, Simon |
author_facet | Ioannoni, Raphael Beaudoin, Jude Lopez-Maury, Luis Codlin, Sandra Bahler, Jurg Labbe, Simon |
author_sort | Ioannoni, Raphael |
collection | PubMed |
description | BACKGROUND: Meiosis is the specialized form of the cell cycle by which diploid cells produce the haploid gametes required for sexual reproduction. Initiation and progression through meiosis requires that the expression of the meiotic genes is precisely controlled so as to provide the correct gene products at the correct times. During meiosis, four temporal gene clusters are either induced or repressed by a cascade of transcription factors. PRINCIPAL FINDINGS: In this report a novel copper-fist-type regulator, Cuf2, is shown to be expressed exclusively during meiosis. The expression profile of the cuf2(+) mRNA revealed that it was induced during middle-phase meiosis. Both cuf2(+) mRNA and protein levels are unregulated by copper addition or starvation. The transcription of cuf2(+) required the presence of a functional mei4(+) gene encoding a key transcription factor that activates the expression of numerous middle meiotic genes. Microscopic analyses of cells expressing a functional Cuf2-GFP protein revealed that Cuf2 co-localized with both homologous chromosomes and sister chromatids during the meiotic divisions. Cells lacking Cuf2 showed an elevated and sustained expression of several of the middle meiotic genes that persisted even during late meiosis. Moreover, cells carrying disrupted cuf2Δ/cuf2Δ alleles displayed an abnormal morphology of the forespore membranes and a dramatic reduction of spore viability. SIGNIFICANCE: Collectively, the results revealed that Cuf2 functions in the timely repression of the middle-phase genes during meiotic differentiation. |
format | Online Article Text |
id | pubmed-3338643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33386432012-05-03 Cuf2 Is a Novel Meiosis-Specific Regulatory Factor of Meiosis Maturation Ioannoni, Raphael Beaudoin, Jude Lopez-Maury, Luis Codlin, Sandra Bahler, Jurg Labbe, Simon PLoS One Research Article BACKGROUND: Meiosis is the specialized form of the cell cycle by which diploid cells produce the haploid gametes required for sexual reproduction. Initiation and progression through meiosis requires that the expression of the meiotic genes is precisely controlled so as to provide the correct gene products at the correct times. During meiosis, four temporal gene clusters are either induced or repressed by a cascade of transcription factors. PRINCIPAL FINDINGS: In this report a novel copper-fist-type regulator, Cuf2, is shown to be expressed exclusively during meiosis. The expression profile of the cuf2(+) mRNA revealed that it was induced during middle-phase meiosis. Both cuf2(+) mRNA and protein levels are unregulated by copper addition or starvation. The transcription of cuf2(+) required the presence of a functional mei4(+) gene encoding a key transcription factor that activates the expression of numerous middle meiotic genes. Microscopic analyses of cells expressing a functional Cuf2-GFP protein revealed that Cuf2 co-localized with both homologous chromosomes and sister chromatids during the meiotic divisions. Cells lacking Cuf2 showed an elevated and sustained expression of several of the middle meiotic genes that persisted even during late meiosis. Moreover, cells carrying disrupted cuf2Δ/cuf2Δ alleles displayed an abnormal morphology of the forespore membranes and a dramatic reduction of spore viability. SIGNIFICANCE: Collectively, the results revealed that Cuf2 functions in the timely repression of the middle-phase genes during meiotic differentiation. Public Library of Science 2012-04-27 /pmc/articles/PMC3338643/ /pubmed/22558440 http://dx.doi.org/10.1371/journal.pone.0036338 Text en Ioannoni 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 Ioannoni, Raphael Beaudoin, Jude Lopez-Maury, Luis Codlin, Sandra Bahler, Jurg Labbe, Simon Cuf2 Is a Novel Meiosis-Specific Regulatory Factor of Meiosis Maturation |
title | Cuf2 Is a Novel Meiosis-Specific Regulatory Factor of Meiosis Maturation |
title_full | Cuf2 Is a Novel Meiosis-Specific Regulatory Factor of Meiosis Maturation |
title_fullStr | Cuf2 Is a Novel Meiosis-Specific Regulatory Factor of Meiosis Maturation |
title_full_unstemmed | Cuf2 Is a Novel Meiosis-Specific Regulatory Factor of Meiosis Maturation |
title_short | Cuf2 Is a Novel Meiosis-Specific Regulatory Factor of Meiosis Maturation |
title_sort | cuf2 is a novel meiosis-specific regulatory factor of meiosis maturation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338643/ https://www.ncbi.nlm.nih.gov/pubmed/22558440 http://dx.doi.org/10.1371/journal.pone.0036338 |
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