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昆虫病原真菌侵染过程中microRNA的全基因组鉴定与分析

Genome-Wide Identification and Analysis of microRNAs during Challenge with the Entomopathogenic Fungus .

作者信息

Xie Jiaqin, Peng Yifan, Xia Yuxian

机构信息

Genetic Engineering Research Center, School of Life Sciences, Chongqing University, Chongqing 401331, China.

Chongqing Engineering Research Center for Fungal Insecticides and Key Laboratory of Gene Function and Regulation Technology under Chongqing Municipal Education Commission, Chongqing 401331, China.

出版信息

J Fungi (Basel). 2021 Apr 14;7(4):295. doi: 10.3390/jof7040295.

Abstract

The resistance of the notorious rice pest to many insecticides has caused significant concerns. Our previous study demonstrated that the fungus CQMa421 shows great potential for the control of this pest, but the interactions between them are still unclear. Thus, we further investigated fungal infection-related microRNAs (miRNAs) in during CQMa421 challenge using Illumina sequencing. In this study, we constructed twenty-four small RNA libraries over different time courses (i.e., 4 h, 8 h, 16 h, and 24 h). A total of 478.62 M clean reads were collected, with each sample producing more than 13.37 M reads, after the removal of low-quality reads. We identified 2324 miRNAs and their 11,076 target genes within the twenty-four libraries by bioinformatics analysis. Differentially expressed miRNAs (DEmiRNAs), including 58 (32 upregulated vs. 26 downregulated), 62 (30 upregulated vs. 32 downregulated), 126 (71 upregulated vs. 55 downregulated), and 109 (40 upregulated vs. 69 downregulated) DEmiRNAs were identified at 4 h, 8 h, 16 h, and 24 h post-infection, respectively. We further conducted Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis to predict the functions of all target genes of DEmiRNAs. These DEmiRNAs targets identified during 24 h of infection were primarily involved in energy metabolism, lysine degradation, the FoxO signaling pathway, ubiquitin-mediated proteolysis, the mRNA surveillance pathway, and the MAPK signaling pathway. Taken together, our results provide essential information for further study of the interactions between the entomopathogenic fungus and at the posttranscriptional level.

摘要

这种臭名昭著的水稻害虫对多种杀虫剂产生抗性,引发了人们的高度关注。我们之前的研究表明,真菌CQMa421在控制这种害虫方面具有巨大潜力,但它们之间的相互作用仍不清楚。因此,我们使用Illumina测序技术进一步研究了CQMa421侵染过程中与真菌感染相关的微小RNA(miRNA)。在本研究中,我们在不同时间进程(即4小时、8小时、16小时和24小时)构建了24个小RNA文库。去除低质量 reads 后,共收集到478.62 M的 clean reads,每个样本产生超过13.37 M的 reads。通过生物信息学分析,我们在这24个文库中鉴定出2324个miRNA及其11,076个靶基因。分别在感染后4小时、8小时、16小时和24小时鉴定出差异表达的miRNA(DEmiRNA),包括58个(32个上调对26个下调)、62个(30个上调对32个下调)、126个(71个上调对55个下调)和109个(40个上调对69个下调)DEmiRNA。我们进一步进行了基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路分析,以预测DEmiRNA所有靶基因的功能。在感染24小时期间鉴定出的这些DEmiRNA靶标主要参与能量代谢、赖氨酸降解、FoxO信号通路、泛素介导的蛋白水解、mRNA监测通路和MAPK信号通路。综上所述,我们的结果为进一步研究昆虫病原真菌与宿主在转录后水平的相互作用提供了重要信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ff/8070897/60ad540369d0/jof-07-00295-g001.jpg

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