Lu Xuke, Wang Xiaoge, Chen Xiugui, Shu Na, Wang Junjuan, Wang Delong, Wang Shuai, Fan Weili, Guo Lixue, Guo Xiaoning, Ye Wuwei
State Key Laboratory of Cotton Biology/Institute of Cotton Research of Chinese Academy of Agricultural Sciences/Key Laboratory for Cotton Genetic Improvement, Anyang, 455000, Henan, China.
College of Agronomy, Xinjiang Agricultural University, Urumqi, 830052, China.
BMC Genomics. 2017 Apr 13;18(1):297. doi: 10.1186/s12864-017-3681-y.
DNA methylation, with a cryptic role in genome stability, gene transcription and expression, is involved in the drought response process in plants, but the complex regulatory mechanism is still largely unknown.
Here, we performed whole-genome bisulfite sequencing (WGBS) and identified long non-coding RNAs on cotton leaves under drought stress and re-watering treatments. We obtained 31,223 and 30,997 differentially methylated regions (representing 2.48% of the genome) after drought stress and re-watering treatments, respectively. Our data also showed that three sequence contexts, including CpG, CHG, CHH, all presented a hyper-methylation pattern under drought stress and were nearly restored to normal levels after the re-watering treatment. Among all the methylation variations, asymmetric CHH methylation was the most consistent with external environments, suggesting that methylation/demethylation in a CHH context may constitute a novel epigenetic modification in response to drought stress. Combined with the targets of long non-coding RNAs, we found that long non-coding RNAs may mediate variations in methylation patterns by splicing into microRNAs. Furthermore, the many hormone-related genes with methylation variations suggested that plant hormones might be a potential mechanism in the drought response.
Future crop-improvement strategies may benefit by taking into account not only the DNA genetic variations in cotton varieties but also the epigenetic modifications of the genome.
DNA甲基化在基因组稳定性、基因转录和表达中发挥着隐秘作用,参与植物的干旱响应过程,但其复杂的调控机制仍 largely 未知。
在此,我们对干旱胁迫和复水处理下的棉花叶片进行了全基因组亚硫酸氢盐测序(WGBS)并鉴定了长链非编码RNA。干旱胁迫和复水处理后,我们分别获得了31,223个和30,997个差异甲基化区域(占基因组的2.48%)。我们的数据还表明,包括CpG、CHG、CHH在内的三种序列背景在干旱胁迫下均呈现高甲基化模式,而复水处理后几乎恢复到正常水平。在所有甲基化变异中,不对称CHH甲基化与外部环境最为一致,表明CHH背景下的甲基化/去甲基化可能构成一种响应干旱胁迫的新型表观遗传修饰。结合长链非编码RNA的靶标,我们发现长链非编码RNA可能通过剪接成微小RNA来介导甲基化模式的变异。此外,许多具有甲基化变异的激素相关基因表明植物激素可能是干旱响应中的一种潜在机制。
未来的作物改良策略不仅可以考虑棉花品种中的DNA遗传变异,还可以考虑基因组的表观遗传修饰,从而从中受益。