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通过深度测序对新型和保守的杨树 microRNA 进行全基因组分析,这些 microRNA 参与病原体应激反应。

Genome-wide profiling of novel and conserved Populus microRNAs involved in pathogen stress response by deep sequencing.

机构信息

National Engineering Laboratory for Tree Breeding, Key Laboratory of Genetics and Breeding in Forest Trees and Ornamental Plants, Ministry of Education, College of Biological Sciences and Biotechnology, Beijing Forestry University, 100083, Beijing, People's Republic of China.

出版信息

Planta. 2012 May;235(5):873-83. doi: 10.1007/s00425-011-1548-z. Epub 2011 Nov 19.

Abstract

MicroRNAs (miRNAs) are small RNAs, generally of 20-23 nt, that down-regulate target gene expression during development, differentiation, growth, and metabolism. In Populus, extensive studies of miRNAs involved in cold, heat, dehydration, salinity, and mechanical stresses have been performed; however, there are few reports profiling the miRNA expression patterns during pathogen stress. We obtained almost 38 million raw reads through Solexa sequencing of two libraries from Populus inoculated and uninoculated with canker disease pathogen. Sequence analyses identified 74 conserved miRNA sequences belonging to 37 miRNA families from 154 loci in the Populus genome and 27 novel miRNA sequences from 35 loci, including their complementary miRNA* strands. Intriguingly, the miRNA* of three conserved miRNAs were more abundant than their corresponding miRNAs. The overall expression levels of conserved miRNAs increased when subjected to pathogen stress, and expression levels of 33 miRNA sequences markedly changed. The expression trends determined by sequencing and by qRT-PCR were similar. Finally, nine target genes for three conserved miRNAs and 63 target genes for novel miRNAs were predicted using computational analysis, and their functions were annotated. Deep sequencing provides an opportunity to identify pathogen-regulated miRNAs in trees, which will help in understanding the regulatory mechanisms of plant defense responses during pathogen infection.

摘要

微小 RNA(miRNA)是 20-23nt 的小 RNA,在发育、分化、生长和代谢过程中下调靶基因的表达。在杨树中,已经进行了广泛的研究,涉及参与冷、热、脱水、盐度和机械胁迫的 miRNA;然而,关于病原体胁迫过程中 miRNA 表达模式的报道很少。我们通过对接种和未接种溃疡病病原体的杨树两个文库进行 Solexa 测序,获得了近 3800 万个原始读数。序列分析从杨树基因组的 154 个基因座中的 37 个 miRNA 家族鉴定出 74 个保守 miRNA 序列和 35 个基因座中的 27 个新 miRNA 序列,包括它们的互补 miRNA链。有趣的是,三个保守 miRNA 的 miRNA比它们对应的 miRNA 更丰富。当受到病原体胁迫时,保守 miRNA 的整体表达水平增加,33 个 miRNA 序列的表达水平明显改变。测序和 qRT-PCR 确定的表达趋势相似。最后,使用计算分析预测了三个保守 miRNA 的 9 个靶基因和 63 个新 miRNA 的靶基因,并对它们的功能进行了注释。深度测序为鉴定树木中受病原体调控的 miRNA 提供了机会,这将有助于理解植物在病原体感染过程中防御反应的调控机制。

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