Chromosome-associated RNA–protein complexes promote pairing of homologous chromosomes during meiosis in Schizosaccharomyces pombe

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Da-Qiao Ding
Kasumi Okamasa
Yuki Katou
Eriko Oya
Jun-ichi Nakayama
Yuji Chikashige
Katsuhiko Shirahige
Tokuko Haraguchi
Yasushi Hiraoka
机构
[1] National Institute of Information and Communications Technology,Advanced ICT Research Institute Kobe
[2] The University of Tokyo,Institute for Quantitative Biosciences
[3] Nagoya City University,Graduate School of Natural Sciences
[4] National Institute for Basic Biology,Division of Chromatin Regulation
[5] Osaka University,Graduate School of Frontier Biosciences
[6] Chuo University,Faculty of Science and Engineering
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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.
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