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通过生物信息学分析和深度测序从与玉米叶斑病相关的新月弯孢菌中鉴定类微小RNA

Identification of microRNA-like RNAs from Curvularia lunata associated with maize leaf spot by bioinformation analysis and deep sequencing.

作者信息

Liu Tong, Hu John, Zuo Yuhu, Jin Yazhong, Hou Jumei

机构信息

Institute of Applied Microbiology and Plant Pathogenic Fungi, College of Agronony, Heilongjiang Bayi Agricultural University, Daqing, 163319, Heilongjiang, People's Republic of China.

State Key Laboratory of Crop Stress Biology in Arid Regions, Northwest A & F University, Yangling, 712100, Shaanxi, People's Republic of China.

出版信息

Mol Genet Genomics. 2016 Apr;291(2):587-96. doi: 10.1007/s00438-015-1128-1. Epub 2015 Oct 19.

Abstract

Deep sequencing of small RNAs is a useful tool to identify novel small RNAs that may be involved in fungal growth and pathogenesis. In this study, we used HiSeq deep sequencing to identify 747,487 unique small RNAs from Curvularia lunata. Among these small RNAs were 1012 microRNA-like RNAs (milRNAs), which are similar to other known microRNAs, and 48 potential novel milRNAs without homologs in other organisms have been identified using the miRBase© database. We used quantitative PCR to analyze the expression of four of these milRNAs from C. lunata at different developmental stages. The analysis revealed several changes associated with germinating conidia and mycelial growth, suggesting that these milRNAs may play a role in pathogen infection and mycelial growth. A total of 8334 target mRNAs for the 1012 milRNAs that were identified, and 256 target mRNAs for the 48 novel milRNAs were predicted by computational analysis. These target mRNAs of milRNAs were also performed by gene ontology and Kyoto Encyclopedia of Genes and Genomes pathway analysis. To our knowledge, this study is the first report of C. lunata's milRNA profiles. This information will provide a better understanding of pathogen development and infection mechanism.

摘要

小RNA深度测序是一种用于鉴定可能参与真菌生长和致病过程的新型小RNA的有用工具。在本研究中,我们使用HiSeq深度测序从新月弯孢霉中鉴定出747,487个独特的小RNA。在这些小RNA中,有1012个类似微小RNA的RNA(milRNA),它们与其他已知的微小RNA相似,并且使用miRBase©数据库鉴定出48个在其他生物体中没有同源物的潜在新型milRNA。我们使用定量PCR分析了新月弯孢霉在不同发育阶段的这4个milRNA的表达。分析揭示了与分生孢子萌发和菌丝体生长相关的几种变化,表明这些milRNA可能在病原体感染和菌丝体生长中发挥作用。通过计算分析预测了1012个milRNA共有8334个靶标mRNA,48个新型milRNA有256个靶标mRNA。这些milRNA的靶标mRNA还进行了基因本体论和京都基因与基因组百科全书途径分析。据我们所知,本研究是关于新月弯孢霉milRNA图谱的首次报道。这些信息将有助于更好地理解病原体的发育和感染机制。

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