Fojtová M, Kovarík A, Matyásek R
Institute of Biophysics, Academy of Sciences of the Czech Republic, Královopolská 135, CZ-612 65, Brno, Czech Republic
Plant Sci. 2001 Mar;160(4):585-593. doi: 10.1016/s0168-9452(00)00411-8.
DNA methylation of chloroplast genome has been studied in a large variety of angiosperm species using restriction enzyme analysis of three genomic loci (totally encompassing about 10% of chloroplast genome) and bisulfite genomic sequencing of tobacco ribulose bisphosphate carboxylase/oxygenase (large subunit) gene (rbcL). Except for CCWGG (W=A or T) sites that were partially refractory to the cleavage with methylation sensitive EcoRII in all loci, no cytosine methylation was found at the CCGG (MspI/HpaII) and several other restriction sites tested. However, EcoRII was unable to completely digest an unmethylated CCWGG site in the cloned rbcL gene on plasmid. Further a bisulfite genomic sequencing performed on EcoRII-restricted DNA failed to show any 5-methylcytosine either within or outside inspected EcoRII sites along the 3' end of rbcL coding region. In conclusion our results do not support evidence for methylated cytosine residues in plant chloroplast genomes and we suggest that results obtained with EcoRII should be interpreted with great care especially when small differences in methylation levels are analysed.
利用对三个基因组位点(总共约占叶绿体基因组的10%)的限制性内切酶分析以及烟草核酮糖二磷酸羧化酶/加氧酶(大亚基)基因(rbcL)的亚硫酸氢盐基因组测序,已经在多种被子植物物种中研究了叶绿体基因组的DNA甲基化。除了在所有位点中对甲基化敏感的EcoRII切割部分抗性的CCWGG(W = A或T)位点外,在CCGG(MspI/HpaII)和其他几个测试的限制性位点未发现胞嘧啶甲基化。然而,EcoRII无法完全消化质粒上克隆的rbcL基因中的未甲基化CCWGG位点。此外,对EcoRII限制的DNA进行的亚硫酸氢盐基因组测序未能在rbcL编码区3'端的检查EcoRII位点内或外显示任何5-甲基胞嘧啶。总之,我们的结果不支持植物叶绿体基因组中存在甲基化胞嘧啶残基的证据,并且我们建议,特别是在分析甲基化水平的微小差异时,应非常谨慎地解释用EcoRII获得的结果。