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. 2019 Dec 6;10:5598. doi: 10.1038/s41467-019-13609-0

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© 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/.

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Fig. 4 — Homologous chromosome pairing at lncRNA accumulation sites. a, b Pairing frequencies were plotted for five substages (I–V). Pairing frequency (%) at the sme2, A55, and C24 loci in WT (blue), rec12⁻ (orange), Δsme2, Δomt3, and ΔlncRNA584 (gray), Δsme2 rec12⁻, Δomt3 rec12⁻, and ΔncRNA.584 rec12⁻ (yellow) Δrhn1 (light blue), seb1⁻ (green), and Δrhn1 seb1⁻ double mutants (purple) was measured in 18–53 cells for each strain; the precise number of cells examined for each strain is provided in Source Data file 4. Percentile rank plots of the distance between homologous loci are shown in Supplementary Fig. 5. Source data for Fig. 4 and Supplementary Fig. 5 and are provided as a Source Data file 4.