Srikakulam Nagesh, Guria Ashirbad, Karanthamalai Jeyalakshmi, Murugesan Vidya, Krishnan Vignesh, Sundaramoorthy Kasthuri, Saha Shakkhar, Singh Rudransh, Victorathisayam Thiveyarajan, Rajapriya Veeraputhiran, Sridevi Ganapathi, Pandi Gopal
Department of Plant Biotechnology, School of Biotechnology, Madurai Kamaraj University, Madurai, India.
Front Genet. 2022 May 30;13:869465. doi: 10.3389/fgene.2022.869465. eCollection 2022.
Sheath blight (ShB) disease, caused by is one of the major biotic stress-oriented diseases that adversely affect the rice productivity worldwide. However, the regulatory mechanisms are not understood yet comprehensively. In the current study, we had investigated the potential roles of miRNAs in economically important indica rice variety Pusa Basmati-1 upon infection by carrying out in-depth, high-throughput small RNA sequencing with a total data size of 435 million paired-end raw reads from rice leaf RNA samples collected at different time points. Detailed data analysis revealed a total of 468 known mature miRNAs and 747 putative novel miRNAs across all the libraries. Target prediction and Gene Ontology functional analysis of these miRNAs were found to be unraveling various cellular, molecular, and biological functions by targeting various plant defense-related genes. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was performed to validate the miRNAs and their putative target genes. Out of the selected miRNA-specific putative target genes, miR395a binding and its cleavage site on pentatricopeptide were determined by 5' RACE-PCR. It might be possible that instigated chloroplast degradation by modulating the pentatricopeptide which led to increased susceptibility to fungal infection.
纹枯病(ShB)由[病原菌名称缺失]引起,是对全球水稻生产力产生不利影响的主要生物胁迫性病害之一。然而,其调控机制尚未得到全面了解。在本研究中,我们通过对不同时间点采集的水稻叶片RNA样本进行深入的高通量小RNA测序(总数据量为4.35亿对末端原始读数),研究了miRNA在经济上重要的籼稻品种Pusa Basmati-1受[病原菌名称缺失]感染后的潜在作用。详细的数据分析显示,所有文库中共有468个已知的成熟miRNA和747个推定的新miRNA。通过对这些miRNA进行靶标预测和基因本体功能分析,发现它们通过靶向各种植物防御相关基因揭示了各种细胞、分子和生物学功能。进行了定量逆转录聚合酶链反应(qRT-PCR)以验证miRNA及其推定的靶标基因。在选定的miRNA特异性推定靶标基因中,通过5' RACE-PCR确定了miR395a在五肽重复序列上的结合及其切割位点。[病原菌名称缺失]可能通过调节五肽重复序列引发叶绿体降解,从而导致对真菌感染的易感性增加。