Department of Forest Science, Texas A&M University, 77843, College Station, TX, USA.
Plant Cell Rep. 1996 Aug;15(11):815-8. doi: 10.1007/BF00233146.
DNA methylation has been associated with gene activity in differentiating and developing plant tissues. The objective of this study was to determine the involvement of methylation in the expression of a gene transferred into carrot (Daucus carota L.) tissues by particle bombardment. Expression of the Dc8-GUS gene construct in response to treatments with 5-azacytidine (S-azaC) and to in vitro methylation by methylases was investigated by histochemical assay of GUS activity. The 5-azaC treatment increased the frequency of Dc8-driven GUS expression in both calli and somatic embryos. The increase occurred with treatment either to E. coli containing the plasmid insert or to the carrot tissues before bombardment. GUS expression, increased by the 5-azaC treatment, was enhanced by ABA treatment of both calli and somatic embryos and was more prominent in the latter. Increased digestion of the 5-azaC-treated plasmid DNA with EcoRII suggested that demethylation had occurred. In vitro methylation of Dc8-GUS by methylases generally resulted in a lower frequency of GUS expression. SssI methylase completely inhibited GUS expression. The level of GUS expression was correlated with the extent of methylation of the plasmid.
DNA 甲基化与植物组织分化和发育过程中的基因活性有关。本研究的目的是确定甲基化在通过粒子轰击转入胡萝卜(Daucus carota L.)组织的基因表达中的作用。通过对 GUS 活性的组织化学分析,研究了 5-氮杂胞苷(S-azaC)处理和甲基酶体外甲基化对 Dc8-GUS 基因构建体表达的影响。5-azaC 处理增加了含有质粒插入物的大肠杆菌或在轰击前的胡萝卜组织中 Dc8 驱动的 GUS 表达的频率。5-azaC 处理增加的 GUS 表达通过 ABA 处理愈伤组织和体细胞胚均得到增强,在后一种情况下更为明显。用 EcoRII 消化 5-azaC 处理的质粒 DNA 表明发生了去甲基化。甲基酶体外甲基化通常导致 GUS 表达频率降低。SssI 甲基酶完全抑制 GUS 表达。GUS 表达水平与质粒的甲基化程度相关。