Wang Yunsheng, Mao Zhenchuan, Yan Jin, Cheng Xinyue, Liu Feng, Xiao Luo, Dai Liangying, Luo Feng, Xie Bingyan
Hunan Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Hunan Agricultural University, Changsha, PR China; Institute of Vegetables and Flowers, CAAS, Beijing, PR China.
Institute of Vegetables and Flowers, CAAS, Beijing, PR China.
PLoS One. 2015 Aug 4;10(8):e0133491. doi: 10.1371/journal.pone.0133491. eCollection 2015.
MicroRNAs play important regulatory roles in eukaryotic lineages. In this paper, we employed deep sequencing technology to sequence and identify microRNAs in M. incognita genome, which is one of the important plant parasitic nematodes. We identified 102 M. incognita microRNA genes, which can be grouped into 71 nonredundant miRNAs based on mature sequences. Among the 71 miRANs, 27 are known miRNAs and 44 are novel miRNAs. We identified seven miRNA clusters in M. incognita genome. Four of the seven clusters, miR-100/let-7, miR-71-1/miR-2a-1, miR-71-2/miR-2a-2 and miR-279/miR-2b are conserved in other species. We validated the expressions of 5 M. incognita microRNAs, including 3 known microRNAs (miR-71, miR-100b and let-7) and 2 novel microRNAs (NOVEL-1 and NOVEL-2), using RT-PCR. We can detect all 5 microRNAs. The expression levels of four microRNAs obtained using RT-PCR were consistent with those obtained by high-throughput sequencing except for those of let-7. We also examined how M. incognita miRNAs are conserved in four other nematodes species: C. elegans, A. suum, B. malayi and P. pacificus. We found that four microRNAs, miR-100, miR-92, miR-279 and miR-137, exist only in genomes of parasitic nematodes, but do not exist in the genomes of the free living nematode C. elegans. Our research created a unique resource for the research of plant parasitic nematodes. The candidate microRNAs could help elucidate the genomic structure, gene regulation, evolutionary processes, and developmental features of plant parasitic nematodes and nematode-plant interaction.
微小RNA在真核生物谱系中发挥着重要的调控作用。在本文中,我们采用深度测序技术对重要的植物寄生线虫南方根结线虫基因组中的微小RNA进行测序和鉴定。我们鉴定出102个南方根结线虫微小RNA基因,基于成熟序列可将其分为71个非冗余的微小RNA。在这71个微小RNA中,27个是已知的微小RNA,44个是新的微小RNA。我们在南方根结线虫基因组中鉴定出7个微小RNA簇。7个簇中的4个,即miR - 100/let - 7、miR - 71 - 1/miR - 2a - 1、miR - 71 - 2/miR - 2a - 2和miR - 279/miR - 2b在其他物种中是保守的。我们使用逆转录聚合酶链反应(RT - PCR)验证了5个南方根结线虫微小RNA的表达,包括3个已知的微小RNA(miR - 71、miR - 100b和let - 7)和2个新的微小RNA(NOVEL - 1和NOVEL - 2)。我们能够检测到所有5个微小RNA。除了let - 7外,通过RT - PCR获得的4个微小RNA的表达水平与通过高通量测序获得的结果一致。我们还研究了南方根结线虫微小RNA在其他四种线虫物种(秀丽隐杆线虫、猪蛔虫、马来布鲁线虫和太平洋小杆线虫)中的保守情况。我们发现4个微小RNA,即miR - 100、miR - 92、miR - 279和miR - 137仅存在于寄生线虫的基因组中,而不存在于自由生活线虫秀丽隐杆线虫的基因组中。我们的研究为植物寄生线虫的研究创造了独特的资源。候选微小RNA有助于阐明植物寄生线虫的基因组结构、基因调控、进化过程、发育特征以及线虫与植物的相互作用。