Sheng Wei, Zhang Aimin, Huang Yueqin, Xue Jianping, Song Yunxian, Chang Li
School of Life Science, Huaibei Normal University, Huaibei, Anhui Key Laboratory of Plant Resources and Biology, Huaibei 235000, China.
Zhongguo Zhong Yao Za Zhi. 2011 Feb;36(3):316-20.
To study mRNA differential expression from microtubes of Pinellia ternata in vitro, and give more information of the molecular mechanism in the formation of microtubers.
DDRT-PCR was used to identify the expressed gene fragments related to the microtubers development of P. ternata in vitro.
Fifteen cDNA fragments differentially expressed in the induction of microtubers of P. ternata in vitro were identified and characterized by using mRNA differential display DDRT-PCR. The deduced amino-acid sequences of six fragments of cDNA showed no significant homology with ESTs and genes in the Genbank databases, and they could be new cDNA fragments. However, the remaining three showed significant homologies with sequences encoding components of eukaryotic translation initiation factor 3 subunit H, MADS-box protein and ethylene signal transcription factor, respectively. Their differential expression patterns were confirmed by semi-quantitative RT-PCR analysis. And the expression level of the induction of microtubers of P. ternata in vitro was different.
研究半夏离体小块茎mRNA的差异表达,为深入了解小块茎形成的分子机制提供更多信息。
采用DDRT-PCR技术鉴定与半夏离体小块茎发育相关的表达基因片段。
运用mRNA差异显示DDRT-PCR技术,鉴定并分析了15个在半夏离体小块茎诱导过程中差异表达的cDNA片段。其中6个cDNA片段推导的氨基酸序列与Genbank数据库中的ESTs和基因无明显同源性,可能为新的cDNA片段。其余3个分别与真核生物翻译起始因子3亚基H、MADS-box蛋白和乙烯信号转录因子的编码序列有显著同源性。半定量RT-PCR分析证实了它们的差异表达模式,且半夏离体小块茎诱导过程中的表达水平存在差异。