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Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe
Pairing of homologous chromosomes in meiosis is essential for sexual reproduction. We have previously demonstrated that the fission yeast sme2 RNA, a meiosis-specific long noncoding RNA (lncRNA), accumulates at the sme2 chromosomal loci and mediates their robust pairing in meiosis. However, the mech...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898681/ https://www.ncbi.nlm.nih.gov/pubmed/31811152 http://dx.doi.org/10.1038/s41467-019-13609-0 |
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author | Ding, Da-Qiao Okamasa, Kasumi Katou, Yuki Oya, Eriko Nakayama, Jun-ichi Chikashige, Yuji Shirahige, Katsuhiko Haraguchi, Tokuko Hiraoka, Yasushi |
author_facet | Ding, Da-Qiao Okamasa, Kasumi Katou, Yuki Oya, Eriko Nakayama, Jun-ichi Chikashige, Yuji Shirahige, Katsuhiko Haraguchi, Tokuko Hiraoka, Yasushi |
author_sort | Ding, Da-Qiao |
collection | PubMed |
description | Pairing of homologous chromosomes in meiosis is essential for sexual reproduction. We have previously demonstrated that the fission yeast sme2 RNA, a meiosis-specific long noncoding RNA (lncRNA), accumulates at the sme2 chromosomal loci and mediates their robust pairing in meiosis. However, the mechanisms underlying lncRNA-mediated homologous pairing have remained elusive. In this study, we identify conserved RNA-binding proteins that are required for robust pairing of homologous chromosomes. These proteins accumulate mainly at the sme2 and two other chromosomal loci together with meiosis-specific lncRNAs transcribed from these loci. Remarkably, the chromosomal accumulation of these lncRNA–protein complexes is required for robust pairing. Moreover, the lncRNA–protein complexes exhibit phase separation properties, since 1,6-hexanediol treatment reversibly disassembled these complexes and disrupted the pairing of associated loci. We propose that lncRNA–protein complexes assembled at specific chromosomal loci mediate recognition and subsequent pairing of homologous chromosomes. |
format | Online Article Text |
id | pubmed-6898681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68986812019-12-09 Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe Ding, Da-Qiao Okamasa, Kasumi Katou, Yuki Oya, Eriko Nakayama, Jun-ichi Chikashige, Yuji Shirahige, Katsuhiko Haraguchi, Tokuko Hiraoka, Yasushi Nat Commun Article Pairing of homologous chromosomes in meiosis is essential for sexual reproduction. We have previously demonstrated that the fission yeast sme2 RNA, a meiosis-specific long noncoding RNA (lncRNA), accumulates at the sme2 chromosomal loci and mediates their robust pairing in meiosis. However, the mechanisms underlying lncRNA-mediated homologous pairing have remained elusive. In this study, we identify conserved RNA-binding proteins that are required for robust pairing of homologous chromosomes. These proteins accumulate mainly at the sme2 and two other chromosomal loci together with meiosis-specific lncRNAs transcribed from these loci. Remarkably, the chromosomal accumulation of these lncRNA–protein complexes is required for robust pairing. Moreover, the lncRNA–protein complexes exhibit phase separation properties, since 1,6-hexanediol treatment reversibly disassembled these complexes and disrupted the pairing of associated loci. We propose that lncRNA–protein complexes assembled at specific chromosomal loci mediate recognition and subsequent pairing of homologous chromosomes. Nature Publishing Group UK 2019-12-06 /pmc/articles/PMC6898681/ /pubmed/31811152 http://dx.doi.org/10.1038/s41467-019-13609-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ding, Da-Qiao Okamasa, Kasumi Katou, Yuki Oya, Eriko Nakayama, Jun-ichi Chikashige, Yuji Shirahige, Katsuhiko Haraguchi, Tokuko Hiraoka, Yasushi Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe |
title | Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe |
title_full | Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe |
title_fullStr | Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe |
title_full_unstemmed | Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe |
title_short | Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe |
title_sort | chromosome-associated rna–protein complexes promote pairing of homologous chromosomes during meiosis in schizosaccharomyces pombe |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898681/ https://www.ncbi.nlm.nih.gov/pubmed/31811152 http://dx.doi.org/10.1038/s41467-019-13609-0 |
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