Université d'Orléans, UFR/Faculté des Sciences, UPRES EA 1207 Laboratoire de Biologie des Ligneux et des Grandes Cultures, INRA USC1328 ARCHE, rue de Chartres, BP6759, 45067 Orléans cedex 2, France.
J Exp Bot. 2013 Jan;64(2):651-63. doi: 10.1093/jxb/ers363.
Sugar beet (Beta vulgaris altissima) is a biennial root crop with an absolute requirement for cold exposure to bolt and flower, a process called vernalization. Global DNA methylation variations have been reported during vernalization in several plants. However, few genes targeted by DNA methylation during vernalization have been described. The objectives of this study were to identify differentially methylated regions and to study their involvement in bolting induction and tolerance. Restriction landmark genome scanning was applied to DNA from shoot apical meristems of sugar beet genotypes, providing a direct quantitative epigenetic assessment of several CG methylated genes without prior knowledge of gene sequence. Several differentially methylated regions exhibiting variations of gene-body DNA methylation and expression during cold exposure and/or between genotypes were identified, including an AROGENATE DEHYDRATASE and two RNA METHYLCYTOSINE TRANSFERASE sequences. One RNA METHYLCYTOSINE TRANSFERASE sequence displayed gene-body hypermethylation and activation of expression, while the other was hypomethylated and inhibited by cold exposure. Global RNA methylation and phenolic compound levels changed during cold exposure in a genotype-dependent way. The use of methyl RNA immunoprecipitation of total RNA and reverse transcription-PCR analysis revealed mRNA methylation in a vernalized bolting-resistant genotype for the FLOWERING LOCUS 1 gene, a repressor of flowering. Finally, Arabidopsis mutants for RNA METHYLCYTOSINE TRANSFERASE and AROGENATE DEHYDRATASE were shown to exhibit, under different environmental conditions, early or late bolting phenotypes, respectively. Overall, the data identified functional targets of DNA methylation during vernalization in sugar beet, and it is proposed that RNA methylation and phenolic compounds play a role in the floral transition.
糖甜菜(Beta vulgaris altissima)是一种两年生的块根作物,绝对需要低温暴露才能抽薹开花,这个过程称为春化。在几种植物的春化过程中,已经报道了全球 DNA 甲基化的变化。然而,在春化过程中,被 DNA 甲基化靶向的基因很少被描述。本研究的目的是鉴定差异甲基化区域,并研究它们在抽薹诱导和耐受中的作用。限制标志基因组扫描应用于糖甜菜基因型的茎尖分生组织 DNA,提供了对几个 CG 甲基化基因的直接定量表观遗传评估,而无需事先了解基因序列。在冷暴露期间和/或在基因型之间,鉴定了几个表现出基因体 DNA 甲基化和表达变化的差异甲基化区域,包括一个 ARONEGATE 脱水酶和两个 RNA 甲基胞嘧啶转移酶序列。一个 RNA 甲基胞嘧啶转移酶序列显示出基因体超甲基化和表达激活,而另一个则被冷暴露抑制。在冷暴露期间,总 RNA 的甲基 RNA 免疫沉淀和反转录-PCR 分析显示了开花基因 FLOWERING LOCUS 1 的 mRNA 甲基化,这是开花的抑制剂。最后,在不同的环境条件下,拟南芥 RNA 甲基胞嘧啶转移酶和 ARONEGATE 脱水酶突变体分别表现出早期或晚期抽薹表型。总的来说,这些数据确定了糖甜菜春化过程中 DNA 甲基化的功能靶点,并且提出 RNA 甲基化和酚类化合物在花转变中起作用。