National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, National Sub-Center of Rapeseed Improvement in Wuhan, Huazhong Agricultural University, Wuhan 430070, China.
Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA.
Int J Mol Sci. 2018 Sep 10;19(9):2689. doi: 10.3390/ijms19092689.
DNA methylation is an essential epigenetic modification that dynamically regulates gene expression during plant development. However, few studies have determined the DNA methylation profiles of male-sterile rapeseed. Here, we conducted a global comparison of DNA methylation patterns between the rapeseed genic male sterile line 7365A and its near-isogenic fertile line 7365B by whole-genome bisulfite sequencing (WGBS). Profiling of the genome-wide DNA methylation showed that the methylation level in floral buds was lower than that in leaves and roots. Besides, a total of 410 differentially methylated region-associated genes (DMGs) were identified in 7365A relative to 7365B. Traditional bisulfite sequencing polymerase chain reaction (PCR) was performed to validate the WGBS data. Eleven DMGs were found to be involved in anther and pollen development, which were analyzed by quantitative PCR. In particular, was hypo-methylated in 7365A, and its expression was up-regulated, which might affect other DMGs and thus control the male sterility. This study provided genome-wide DNA methylation profiles of floral buds and important clues for revealing the molecular mechanism of genic male sterility in rapeseed.
DNA 甲基化是一种重要的表观遗传修饰,可在植物发育过程中动态调控基因表达。然而,很少有研究确定了雄性不育油菜的 DNA 甲基化图谱。在这里,我们通过全基因组亚硫酸氢盐测序(WGBS)对油菜基因雄性不育系 7365A 与其近等基因可育系 7365B 之间的 DNA 甲基化模式进行了全面比较。全基因组 DNA 甲基化分析表明,花蕾中的甲基化水平低于叶片和根中的甲基化水平。此外,在 7365A 相对于 7365B 中总共鉴定出 410 个差异甲基化区相关基因(DMGs)。通过传统的亚硫酸氢盐测序聚合酶链反应(PCR)对 WGBS 数据进行了验证。通过定量 PCR 分析了 11 个与花药和花粉发育相关的 DMGs。特别是在 7365A 中,DMG 被低甲基化,其表达上调,这可能影响其他 DMGs,从而控制雄性不育。这项研究提供了花蕾的全基因组 DNA 甲基化图谱,并为揭示油菜基因雄性不育的分子机制提供了重要线索。