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白桦MADS基因的克隆及序列分析

Cloning and Sequence Analysis of MADS Gene of Betula platyphylla

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【作者】 魏志刚魏继承杨传平刘关君

【Author】 Wei Zhigang(the Key Laboratory of Forest Tree Genetic Improvement and Biotechnology of Ministry of Education, Northeast Forestry University, Harbin 150040, P. R. China); Wei Jicheng (Mudanjiang Normal College); Yang Chuanping, Liu Guanjun(the Key Laboratory of Forest Tree Genetic Improvement and Biotechnology of Ministry of Education, Northeast Forestry University)

【机构】 林木遗传育种与生物技术教育部重点实验室(东北林业大学)牡丹江师范学院林木遗传育种与生物技术教育部重点实验室(东北林业大学) 哈尔滨150040哈尔滨

【摘要】 在分析了欧洲白桦MADS3与拟南芥AP1中的保守性后,设计了一对引物。以白桦雄花芽为材料,从总RNA中通过RT-PCR分离得到一个MADS基因,其cDNA长738bp,包含了基因完整的编码序列,白桦MADS基因与已发表的欧洲白桦MADS3基因仅相差6个碱基,同源性高达99%;推导氨基酸序列的差异为5个,同源性达97%。分析其氨基酸序列表明,存在典型的MADS MEF2转录因子结构域和K-box结构域。

【Abstract】 A pair of primers was designed based on the analysis of MADS3 from Betula petulla and AP1 from Arabidopsis thaliana. One MADS gene was cloned from total RNA using the male bloom of B. petulla as material. DNA sequencing analysis showed that the size of the cloned MADS cDNAs were 738 base pairs, which carried the entire coding sequences. Comparison analysis exhibited differences in only six base pairs between the cloned MADS and the reported, and sequence homology reached ninetynine percent, which resulted in an alteration of five deduced amino acids and ninety-seven percent of sequence homology. Moreover, the DNA sequencing analysis showed a typical transcriptional factor of MADS MEF2 and K-box domain.

【基金】 国家自然科学基金项目资助(39970627)。
  • 【文献出处】 东北林业大学学报 ,Journal of Northeast Forestry University , 编辑部邮箱 ,2007年01期
  • 【分类号】S792.153
  • 【被引频次】9
  • 【下载频次】428
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