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. 2018 Aug 29;9:3516. doi: 10.1038/s41467-018-05829-7

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© The Author(s) 2018

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. 1 — Cloning and characterization of LAIR. a Genome map of the LRK gene cluster and LAIR. The LRK genes are located in a 51.3-kb region on chromosome 2 of Nipponbare PAC clone AP007224. LncRNA LAIR (JX512726), which includes six exons, is transcribed from the antisense strand of LRK1. Additionally, LRK1 is in the first LAIR intron, with no overlap between the two transcripts. b–d Phenotypes of wild-type (WT), antisense RNAi-LAIR (Anti-LAIR), and LAIR-overexpressing (LAIR) transgenic rice plants. Growth traits of T₃ transgenic lines were investigated, including mature plant phenotype (b), primary panicle size (c), and number of panicles per plant (d). e Growth traits of Anti-LAIR and LAIR transgenic lines. Student’s t-test: *P < 0.05. Data are presented as the mean ± standard deviation (n = 12)