Department of Molecular Biology & Genetic Engineering, College of Basic Sciences & Humanities, GB Pant University of Agriculture & Technology, Pantnagar, US Nagar 263 145, India.
Mol Biol Rep. 2012 Mar;39(3):2089-95. doi: 10.1007/s11033-011-0956-2. Epub 2011 Jun 4.
In the present study Dof1 gene of finger millet was cloned and sequenced. In silico analysis reveals 61% identity with the Sorghum bicolor and 57% identity with the Oryza sativa Dof1 sequence. A comparative analysis of gene sequences from different crops and three finger millet genotypes {Brown (PRM-1), Golden (PRM-701) and White (PRM-801)} differing in grain colour, yield and photosynthetic efficiency showed a high degree of sequence identity of Dof1 sequence gene ranging from 22 to 70% as evident from distance matrix of the built phylogenetic tree showing two major clusters. A total of five conserved motifs were observed in Dof1 sequences of different cereals. Motif 1 with multilevel consensus sequence CKNCRRYWTKGGAMRNVPVG contains zinc finger Dof domain. Motif 3 and motif 5 contains protein kinase phosphorylation site. Motif 2 contains Dof domain and zinc finger N-glycosylation site while motif 4 is involved in Zinc finger type profiling. Further, we studied the spatial distribution of Dof1 gene in three vegetative tissues (root, stem and flag leaf) as well as four stages of developing spikes (S1, S2, S3 and S4) of the three finger millet genotypes using qualitative and quantitative PCR based approaches. Physiological parameters (plant height, leaf area, chlorophyll content, SPAD value and photosynthetic efficiency) at the time of flowering was found to be highest in white (PRM-801) genotype followed by golden (PRM-701) and brown (PRM-1) genotype. Semi-quantitative RT-PCR and quantitative real-time PCR analysis revealed that the expression of Dof1 is highest in leaves and lowest in roots, which suggests its role in regulation of photosynthesis-related genes and carbon skeleton synthesis. Also at grain maturity stage, expression of Dof1 was higher in white (PRM-801) genotype followed by golden (PRM-701) and brown (PRM-1) genotype. The result is suggestive of Dof1 role in the accumulation of grain protein and yield attribute through regulation of key enzymes involved in source to sink relationship during grain filling stage.
在本研究中,克隆并测序了手指小米的 Dof1 基因。计算机分析显示,它与高粱的相似度为 61%,与水稻的相似度为 57%。对不同作物和三个在籽粒颜色、产量和光合效率方面存在差异的手指小米基因型(Brown(PRM-1)、Golden(PRM-701)和 White(PRM-801))的基因序列进行比较分析表明,Dof1 基因序列具有高度的序列同一性,范围在 22%到 70%之间,这从构建的系统发育树的距离矩阵中显而易见,该矩阵显示了两个主要聚类。在不同谷物的 Dof1 序列中观察到了总共五个保守基序。基序 1 具有多层次共识序列 CKNCRRYWTKGGAMRNVPVG,包含锌指 Dof 结构域。基序 3 和基序 5 包含蛋白激酶磷酸化位点。基序 2 包含 Dof 结构域和锌指 N-糖基化位点,而基序 4 参与锌指类型分析。此外,我们使用基于定性和定量 PCR 的方法研究了 Dof1 基因在三个手指小米基因型的三个营养组织(根、茎和旗叶)以及四个穗发育阶段(S1、S2、S3 和 S4)中的空间分布。开花时,发现白色(PRM-801)基因型的生理参数(株高、叶面积、叶绿素含量、SPAD 值和光合效率)最高,其次是金色(PRM-701)和棕色(PRM-1)基因型。半定量 RT-PCR 和定量实时 PCR 分析显示,Dof1 在叶片中的表达最高,在根中的表达最低,这表明它在调节光合作用相关基因和碳骨架合成中发挥作用。在籽粒成熟阶段,白色(PRM-801)基因型的 Dof1 表达最高,其次是金色(PRM-701)和棕色(PRM-1)基因型。结果表明,Dof1 通过调节籽粒灌浆阶段源到汇关系中的关键酶,在积累籽粒蛋白和产量性状方面发挥作用。