Department of Pharmaceutical Sciences, Biomanufacturing Research Institute and Technology Enterprise, North Carolina Central University, Durham, NC 27707, USA.
J Exp Bot. 2010 Mar;61(5):1483-93. doi: 10.1093/jxb/erq020. Epub 2010 Feb 18.
Variegated plants provide a valuable tool for studying chloroplast biogenesis by allowing direct comparison between green and white/yellow sectors within the same leaf. While variegated plants are abundant in nature, the mechanism of leaf variegation remains largely unknown. Current studies are limited to a few mutants in model plant species, and are complicated by the potential for cross-contamination during dissection of leaf tissue into contrasting sectors. To overcome these obstacles, an alternative approach was explored using tissue-culture techniques to regenerate plantlets from unique sectors. Stable green and pale yellow plants were developed from a naturally variegated Epipremnum aureum 'Golden Pothos'. By comparing the gene expression between green and pale yellow plants using suppression subtractive hybridization in conjunction with homologous sequence search, nine down-regulated and 18 up-regulated genes were identified in pale yellow plants. Transcript abundance for EaZIP (Epipremnum aureum leucine zipper), a nuclear gene homologue of tobacco NTZIP and Arabidopsis CHL27, was reduced more than 4000-fold in qRT-PCR analysis. EaZIP encodes the Mg-protoporphyrin IX monomethyl ester cyclase, one of the key enzymes in the chlorophyll biosynthesis pathway. Examination of EaZIP expression in naturally variegated 'Golden Pothos' confirmed that EaZIP transcript levels were correlated with leaf chlorophyll contents, suggesting that this gene plays a major role in the loss of chlorophyll in the pale yellow sectors of E. aureum 'Golden Pothos'. This study further suggests that tissue-culture regeneration of plantlets from different coloured sectors of variegated leaves can be used to investigate the underlying mechanisms of variegation.
斑叶植物为研究叶绿体生物发生提供了一个有价值的工具,因为它可以在同一片叶子内的绿色和白色/黄色区域之间进行直接比较。虽然自然界中存在大量的斑叶植物,但叶片斑驳的形成机制在很大程度上仍然未知。目前的研究仅限于少数模式植物物种的突变体,而且由于在将叶片组织切割成不同区域时可能发生交叉污染,研究变得复杂。为了克服这些障碍,我们探索了一种使用组织培养技术从独特区域再生植物的替代方法。从天然斑驳的 Epipremnum aureum 'Golden Pothos' 中使用组织培养技术再生了稳定的绿色和淡黄绿色植株。通过使用抑制性差减杂交结合同源序列搜索,比较绿色和淡黄绿色植株之间的基因表达,在淡黄绿色植株中鉴定出 9 个下调和 18 个上调基因。EaZIP(Epipremnum aureum leucine zipper)的转录丰度在 qRT-PCR 分析中降低了 4000 倍以上,EaZIP 是烟草 NTZIP 和拟南芥 CHL27 的核基因同源物。EaZIP 编码 Mg-原卟啉 IX 单甲基酯环化酶,这是叶绿素生物合成途径中的关键酶之一。在天然斑驳的“Golden Pothos”中检查 EaZIP 的表达,证实 EaZIP 转录本水平与叶片叶绿素含量相关,表明该基因在 E. aureum 'Golden Pothos' 淡黄绿色区域中叶绿素丢失中起主要作用。这项研究进一步表明,从斑驳叶片的不同颜色区域再生植物的组织培养可以用于研究斑驳形成的潜在机制。