Xi Qian-Yun, Xiong Yuan-Yan, Wang Yuan-Mei, Cheng Xiao, Qi Qi-En, Shu Gang, Wang Song-Bo, Wang Li-Na, Gao Ping, Zhu Xiao-Tong, Jiang Qing-Yan, Zhang Yong-Liang, Liu Li
Guangdong Provincial Key Laboratory of Agro-animal Genomics and Molecular Breeding, South China Agricultural University, 483 Wushan Road, Guangzhou, 510642, China,
Mol Biol Rep. 2015 Jan;42(1):61-9. doi: 10.1007/s11033-014-3740-2. Epub 2014 Sep 17.
Of late years, a large amount of conserved and species-specific microRNAs (miRNAs) have been performed on identification from species which are economically important but lack a full genome sequence. In this study, Solexa deep sequencing and cross-species miRNA microarray were used to detect miRNAs in white shrimp. We identified 239 conserved miRNAs, 14 miRNA* sequences and 20 novel miRNAs by bioinformatics analysis from 7,561,406 high-quality reads representing 325,370 distinct sequences. The all 20 novel miRNAs were species-specific in white shrimp and not homologous in other species. Using the conserved miRNAs from the miRBase database as a query set to search for homologs from shrimp expressed sequence tags (ESTs), 32 conserved computationally predicted miRNAs were discovered in shrimp. In addition, using microarray analysis in the shrimp fed with Panax ginseng polysaccharide complex, 151 conserved miRNAs were identified, 18 of which were significant up-expression, while 49 miRNAs were significant down-expression. In particular, qRT-PCR analysis was also performed for nine miRNAs in three shrimp tissues such as muscle, gill and hepatopancreas. Results showed that these miRNAs expression are tissue specific. Combining results of the three methods, we detected 20 novel and 394 conserved miRNAs. Verification with quantitative reverse transcription (qRT-PCR) and Northern blot showed a high confidentiality of data. The study provides the first comprehensive specific miRNA profile of white shrimp, which includes useful information for future investigations into the function of miRNAs in regulation of shrimp development and immunology.
近年来,人们已从许多具有经济重要性但缺乏全基因组序列的物种中鉴定出大量保守的和物种特异性的微小RNA(miRNA)。在本研究中,采用Solexa深度测序和跨物种miRNA微阵列技术检测凡纳滨对虾中的miRNA。通过生物信息学分析,我们从代表325,370个不同序列的7,561,406条高质量读段中鉴定出239个保守miRNA、14个miRNA*序列和20个新miRNA。所有20个新miRNA均为凡纳滨对虾所特有,在其他物种中无同源性。以miRBase数据库中的保守miRNA作为查询集,在凡纳滨对虾表达序列标签(EST)中搜索同源物,发现了32个保守的通过计算预测的miRNA。此外,对饲喂人参多糖复合物的凡纳滨对虾进行微阵列分析,鉴定出151个保守miRNA,其中18个显著上调,49个显著下调。特别地,还对肌肉、鳃和肝胰腺这三种凡纳滨对虾组织中的9个miRNA进行了qRT-PCR分析。结果表明这些miRNA的表达具有组织特异性。综合三种方法的结果,我们检测到20个新miRNA和394个保守miRNA。定量逆转录(qRT-PCR)和Northern印迹验证显示数据具有高度可信度。本研究首次提供了凡纳滨对虾全面的特异性miRNA图谱,为今后研究miRNA在凡纳滨对虾发育和免疫调节中的功能提供了有用信息。