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. 2018 Apr 11;8:5860. doi: 10.1038/s41598-018-23985-0

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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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Phenotypes of the wild-type and transgenic Arabidopsis thaliana plants overexpressing MnMADS33, MnMADS50, and MnMADS7. (A–C) Five-week-old wild and transgenic seedlings under long-day conditions (16/8 h of light/dark). (D) Expression levels of MnMADS33, MnMADS50, and MnMADS7 determined by qRT-PCR in wild-type and transgenic A. thaliana. (E) qRT-PCR analyses of AtSOC1 and AtFT in wild-type and transgenic A. thaliana. (F) The leaf numbers of rosette in wild and transgenic A. thaliana plants. For qRT-PCR analyses in (D,E), A. thaliana Actin7 is used as the internal control. Error bars represent the standard deviations of three independent experiments. Significant differences are indicated by different lower-case letters resulting from one-way Duncan’s test (P < 0.05).