Pradhan Bhubaneswar, Naqvi Afsar Raza, Saraf Shradha, Mukherjee Sunil Kumar, Dey Nrisingha
Division of Gene Function and Regulation, Institute of Life Sciences, Nalco Square, Chandrasekharpur, Bhubaneswar 751023, Odisha, India.
Plant Molecular Biology Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Virus Res. 2015 Jan 2;195:183-95. doi: 10.1016/j.virusres.2014.09.001. Epub 2014 Sep 16.
Tomato leaf curl New Delhi virus (ToLCNDV) infects tomato (Solanum lycopersicum) plants and causes severe crop losses. As the microRNAs (miRNAs) are deregulated during stressful events, such as biotic stress, we wanted to study the effect of ToLCNDV infection on tomato miRNAs. We constructed two libraries, isolating small RNAs (sRNAs) from healthy (HT) and ToLCNDV infected (IT) tomato leaves, and sequenced the library-specific sRNAs using the next generation sequencing (NGS) approach. These data helped predict 112 mature miRNA sequences employing the miRDeep-P program. A substantial number (58) of the sequences were 24-mer in size, which was a bit surprising. Based on the calculation of precision values, 53 novel miRNAs were screened from the predicted sequences. Nineteen of these were chosen for expression analysis; a northern blot analysis showed 15 to be positive. Many of the predicted miRNAs were up-regulated following viral infection. The target genes of the miRNAs were also predicted and the expression analysis of selected transcripts showed a typical inverse relation between the accumulation of target transcripts and the abundance of corresponding miRNAs. Furthermore, the cleavage sites of the target transcripts for three novel miRNAs were mapped, confirming the correct annotation of the miRNA-targets. The sRNA deep sequencing clearly revealed that the virus modulated global miRNA expression in the host. The validated miRNAs (Tom_4; Tom_14; Tom_17; Tom_21; Tom_29; Tom_43) could be valuable tools for understanding the ToLCNDV-tomato interaction, ultimately leading to the development of a virus-resistant tomato plant.
番茄卷叶新德里病毒(ToLCNDV)感染番茄(Solanum lycopersicum)植株并导致严重的作物损失。由于微小RNA(miRNA)在诸如生物胁迫等应激事件期间会失调,我们想要研究ToLCNDV感染对番茄miRNA的影响。我们构建了两个文库,从健康(HT)和ToLCNDV感染(IT)的番茄叶片中分离小RNA(sRNA),并使用下一代测序(NGS)方法对文库特异性sRNA进行测序。这些数据有助于使用miRDeep-P程序预测112个成熟miRNA序列。其中相当数量(58个)的序列长度为24个核苷酸,这有点令人惊讶。基于精确值的计算,从预测序列中筛选出53个新的miRNA。其中19个被选用于表达分析;Northern印迹分析显示15个呈阳性。许多预测的miRNA在病毒感染后上调。还预测了miRNA的靶基因,所选转录本的表达分析显示靶转录本的积累与相应miRNA的丰度之间存在典型的负相关关系。此外,绘制了三种新miRNA的靶转录本的切割位点,证实了miRNA-靶标的正确注释。sRNA深度测序清楚地表明病毒调节宿主中的全局miRNA表达。经过验证的miRNA(Tom_4;Tom_14;Tom_17;Tom_21;Tom_29;Tom_43)可能是理解ToLCNDV与番茄相互作用的有价值工具,最终导致抗病毒番茄植株的开发。