Abstract

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.

Details

Title
Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe
Author
Da-Qiao, Ding 1   VIAFID ORCID Logo  ; Okamasa, Kasumi 1 ; Katou, Yuki 2 ; Oya, Eriko 3   VIAFID ORCID Logo  ; Nakayama, Jun-ichi 4   VIAFID ORCID Logo  ; Chikashige, Yuji 1 ; Shirahige, Katsuhiko 2 ; Haraguchi, Tokuko 5   VIAFID ORCID Logo  ; Hiraoka, Yasushi 5   VIAFID ORCID Logo 

 Advanced ICT Research Institute Kobe, National Institute of Information and Communications Technology, Kobe, Japan 
 Institute for Quantitative Biosciences, The University of Tokyo, Tokyo, Japan 
 Graduate School of Natural Sciences, Nagoya City University, Nagoya, Japan; Faculty of Science and Engineering, Chuo University, Tokyo, Japan 
 Graduate School of Natural Sciences, Nagoya City University, Nagoya, Japan; Division of Chromatin Regulation, National Institute for Basic Biology, Okazaki, Japan 
 Advanced ICT Research Institute Kobe, National Institute of Information and Communications Technology, Kobe, Japan; Graduate School of Frontier Biosciences, Osaka University, Suita, Japan 
Pages
1-12
Publication year
2019
Publication date
Dec 2019
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2322188218
Copyright
© 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.