Lomate Purushottam R, Mahajan Neha S, Kale Sandip M, Gupta Vidya S, Giri Ashok P
Plant Molecular Biology Unit, Division of Biochemical Sciences, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, MS, India.
Plant Molecular Biology Unit, Division of Biochemical Sciences, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, MS, India.
Insect Biochem Mol Biol. 2014 Nov;54:129-37. doi: 10.1016/j.ibmb.2014.09.008. Epub 2014 Sep 28.
The present investigation is an effort to determine the possible roles of microRNAs (miRNAs) in the regulation of protease gene expression in Helicoverpa armigera upon exposure to plant protease inhibitors (PIs). Using Illumina platform, deep sequencing of 12 small RNA libraries was performed from H. armigera larvae fed on artificial diet (AD) or recombinant Capsicum annuum PI-7 (rCanPI-7) incorporated diet, at various time intervals (0.5, 2, 6, 12, 24, and 48 h). Sequencing data were analyzed with miRDeep2 software; a total of 186 unique miRNAs were identified from all the 12 libraries, out of which 96 were conserved while 90 were novel. These miRNAs showed all the conserved characteristics of insect miRNAs. Homology analysis revealed that most of the identified miRNAs were insect-specific, and more than 50 miRNAs were Lepidoptera-specific. Several candidate miRNAs (conserved and novel) were differentially expressed in rCanPI-7 fed larvae as compared to the larvae fed on AD. H. armigera miRNAs were found to have target sites in several protease genes as well as in protease regulation related genes such as serine PI and immune reactive PI. As expected, negative correlation in the relative abundance of miRNAs and their target mRNAs was evident from qualitative real time polymerase chain reaction analysis. The investigation revealed potential roles of miRNAs in H. armigera protease gene regulation.
本研究旨在确定微小RNA(miRNA)在棉铃虫暴露于植物蛋白酶抑制剂(PI)时对蛋白酶基因表达调控中可能发挥的作用。利用Illumina平台,对取食人工饲料(AD)或添加重组辣椒PI-7(rCanPI-7)饲料的棉铃虫幼虫在不同时间间隔(0.5、2、6、12、24和48小时)的12个小RNA文库进行了深度测序。测序数据用miRDeep2软件进行分析;从所有12个文库中共鉴定出186个独特的miRNA,其中96个是保守的,90个是新的。这些miRNA表现出昆虫miRNA的所有保守特征。同源性分析表明,鉴定出的大多数miRNA是昆虫特异性的,超过50个miRNA是鳞翅目特异性的。与取食AD的幼虫相比,几种候选miRNA(保守的和新的)在取食rCanPI-7的幼虫中差异表达。发现棉铃虫miRNA在几个蛋白酶基因以及蛋白酶调节相关基因(如丝氨酸PI和免疫反应性PI)中具有靶位点。正如预期的那样,从定性实时聚合酶链反应分析中可以明显看出miRNA及其靶mRNA相对丰度的负相关。该研究揭示了miRNA在棉铃虫蛋白酶基因调控中的潜在作用。