The Key Laboratory of Plant Cell Engineering and Germplasm Innovation, School of Life Sciences, Shandong University, Jinan, Shandong, China.
PLoS One. 2012;7(7):e41274. doi: 10.1371/journal.pone.0041274. Epub 2012 Jul 18.
Epigenetic modification contributes to the regulation of gene expression and plant development under salinity stress. Here we describe the identification of 49 soybean transcription factors by microarray analysis as being inducible by salinity stress. A semi-quantitative RT-PCR-based expression assay confirmed the salinity stress inducibility of 45 of these 49 transcription factors, and showed that ten of them were up-regulated when seedlings were exposed to the demethylation agent 5-aza-2-deoxycytidine. Salinity stress was shown to affect the methylation status of four of these ten transcription factors (one MYB, one b-ZIP and two AP2/DREB family members) using a combination of bisulfite sequencing and DNA methylation-sensitive DNA gel blot analysis. ChIP analysis indicated that the activation of three of the four DNA methylated transcription factors was correlated with an increased level of histone H3K4 trimethylation and H3K9 acetylation, and/or a reduced level of H3K9 demethylation in various parts of the promoter or coding regions. Our results suggest a critical role for some transcription factors' activation/repression by DNA methylation and/or histone modifications in soybean tolerance to salinity stress.
表观遗传修饰有助于调节盐胁迫下的基因表达和植物发育。在这里,我们通过微阵列分析描述了 49 种大豆转录因子的鉴定,这些转录因子可被盐胁迫诱导。基于半定量 RT-PCR 的表达分析证实了这 49 种转录因子中的 45 种对盐胁迫具有诱导性,并且表明当幼苗暴露于去甲基化剂 5-氮杂-2-脱氧胞苷时,其中 10 种被上调。使用亚硫酸氢盐测序和 DNA 甲基化敏感 DNA 凝胶印迹分析的组合,表明这 10 种转录因子中的四种(一个 MYB、一个 b-ZIP 和两个 AP2/DREB 家族成员)的甲基化状态受到盐胁迫的影响。ChIP 分析表明,在启动子或编码区的不同部位,三个 DNA 甲基化转录因子的激活与组蛋白 H3K4 三甲基化和 H3K9 乙酰化水平的增加以及/或 H3K9 去甲基化水平的降低相关。我们的结果表明,一些转录因子的激活/抑制作用通过 DNA 甲基化和/或组蛋白修饰在大豆对盐胁迫的耐受性中起着关键作用。