Prakash A P, Kumar P P
Plant Morphogenesis Laboratory, School of Biological Sciences, The National University of Singapore, Kent Ridge Crescent, Singapore 119260, Fax no.: +65-779-5671, E-mail:
Plant Cell Rep. 1997 Jul;16(10):719-724. doi: 10.1007/s002990050309.
Shoot bud regeneration from Petunia leaf disks was inhibited when they were cultured with the demethylating agents, 5-azacytidine (AzaC) and 5-aza-2'-deoxycytidine (AzadC), in shoot induction (SI) medium. Explants induced shoot primordia if they were transferred after 1 week from the medium containing the drugs to medium without drugs. The fresh weight of leaf disks cultured on SI medium for 2 weeks in the presence of the drugs was 60-80% lower when compared to control shoot-forming cultures. Internode length was reduced when shoots were transferred to phytohormone-free Murashige and Skoog medium containing the drugs. However, no other morphological abnormalities were seen in these shoots, even at 20 µM AzaC or 5 µM AzadC. Coupled restriction enzyme digestion (with HpaII and MspI) and random amplification of genomic DNA was performed to detect the level of methylation of CCGG sites in the DNA of the explants exposed to AzaC and AzadC. Over 15 amplified bands were detectable in the control. Five of these bands were absent in the amplified products when digested DNA from the drug-treated explants was used as the template, showing that hypomethylation of DNA had occurred. This suggests that inhibition of shoot bud formation in the presence of the drugs AzaC and AzadC may be due to the altered methylation status.
矮牵牛叶片圆盘在芽诱导(SI)培养基中与去甲基化剂5-氮杂胞苷(AzaC)和5-氮杂-2'-脱氧胞苷(AzadC)一起培养时,其芽再生受到抑制。如果外植体在含有药物的培养基中培养1周后转移到不含药物的培养基中,它们会诱导出芽原基。与对照芽形成培养物相比,在药物存在下于SI培养基中培养2周的叶片圆盘鲜重降低了60-80%。当芽转移到含有药物的无植物激素的Murashige和Skoog培养基中时,节间长度缩短。然而,即使在20 µM AzaC或5 µM AzadC的情况下,这些芽中也未观察到其他形态异常。进行了限制性内切酶联合消化(用HpaII和MspI)和基因组DNA的随机扩增,以检测暴露于AzaC和AzadC的外植体DNA中CCGG位点的甲基化水平。在对照中可检测到超过15条扩增带。当使用来自药物处理外植体的消化DNA作为模板时,在扩增产物中缺少其中5条带,表明DNA发生了低甲基化。这表明在药物AzaC和AzadC存在下芽形成的抑制可能是由于甲基化状态的改变。