Huck Institute of Life Sciences, The Pennsylvania State University, University Park, PA 16802, USA.
BMC Plant Biol. 2010 Nov 15;10:248. doi: 10.1186/1471-2229-10-248.
The Arabidopsis thaliana NPR1 gene encodes a transcription coactivator (NPR1) that plays a major role in the mechanisms regulating plant defense response. After pathogen infection and in response to salicylic acid (SA) accumulation, NPR1 translocates from the cytoplasm into the nucleus where it interacts with other transcription factors resulting in increased expression of over 2000 plant defense genes contributing to a pathogen resistance response.
A putative Theobroma cacao NPR1 cDNA was isolated by RT-PCR using degenerate primers based on homologous sequences from Brassica, Arabidopsis and Carica papaya. The cDNA was used to isolate a genomic clone from Theobroma cacao containing a putative TcNPR1 gene. DNA sequencing revealed the presence of a 4.5 kb coding region containing three introns and encoding a polypeptide of 591 amino acids. The predicted TcNPR1 protein shares 55% identity and 78% similarity to Arabidopsis NPR1, and contains each of the highly conserved functional domains indicative of this class of transcription factors (BTB/POZ and ankyrin repeat protein-protein interaction domains and a nuclear localization sequence (NLS)). To functionally define the TcNPR1 gene, we transferred TcNPR1 into an Arabidopsis npr1 mutant that is highly susceptible to infection by the plant pathogen Pseudomonas syringae pv. tomato DC3000. Driven by the constitutive CaMV35S promoter, the cacao TcNPR1 gene partially complemented the npr1 mutation in transgenic Arabidopsis plants, resulting in 100 fold less bacterial growth in a leaf infection assay. Upon induction with SA, TcNPR1 was shown to translocate into the nucleus of leaf and root cells in a manner identical to Arabidopsis NPR1. Cacao NPR1 was also capable of participating in SA-JA signaling crosstalk, as evidenced by the suppression of JA responsive gene expression in TcNPR1 overexpressing transgenic plants.
Our data indicate that the TcNPR1 is a functional ortholog of Arabidopsis NPR1, and is likely to play a major role in defense response in cacao. This fundamental knowledge can contribute to breeding of disease resistant cacao varieties through the application of molecular markers or the use of transgenic strategies.
拟南芥 NPR1 基因编码一种转录共激活因子(NPR1),在调节植物防御反应的机制中发挥主要作用。在病原体感染后并响应水杨酸(SA)积累时,NPR1 从细胞质易位到细胞核,在那里与其他转录因子相互作用,导致超过 2000 种植物防御基因的表达增加,从而导致对病原体抗性反应。
使用基于 Brassica、Arabidopsis 和 Carica papaya 的同源序列的简并引物通过 RT-PCR 分离出可可 NPR1 的推定 cDNA。使用该 cDNA 从可可中分离出包含推定的 TcNPR1 基因的基因组克隆。DNA 测序揭示了存在一个 4.5kb 的编码区,其中包含三个内含子,并编码一个 591 个氨基酸的多肽。预测的 TcNPR1 蛋白与拟南芥 NPR1 具有 55%的同一性和 78%的相似性,并包含该类转录因子(BTB/POZ 和锚蛋白重复蛋白-蛋白相互作用域和核定位序列(NLS))的每个高度保守的功能域。为了对 TcNPR1 基因进行功能定义,我们将 TcNPR1 转移到拟南芥 npr1 突变体中,该突变体对植物病原体丁香假单胞菌 pv tomato DC3000 的感染高度敏感。在组成型 CaMV35S 启动子的驱动下,可可 TcNPR1 基因在转基因拟南芥植物中部分补充了 npr1 突变,导致叶感染测定中细菌生长减少 100 倍。在用 SA 诱导后,TcNPR1 被证明以与拟南芥 NPR1 相同的方式易位到叶和根细胞的细胞核中。可可 NPR1 还能够参与 SA-JA 信号串扰,因为在 TcNPR1 过表达转基因植物中,JA 响应基因的表达受到抑制。
我们的数据表明,TcNPR1 是拟南芥 NPR1 的功能同源物,并且可能在可可的防御反应中发挥主要作用。这一基础知识可以通过应用分子标记或使用转基因策略来促进抗病可可品种的培育。