Li Zhigang, Yang Jun, Peng Junbo, Cheng Zhihua, Liu Xinsen, Zhang Ziding, Bhadauria Vijai, Zhao Wensheng, Peng You-Liang
College of Plant Protection/Key Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pests, Ministry of Education, Hainan University, Haikou, China.
Ministry of Agriculture and Rural Affairs Key Laboratory of Pest Monitoring and Green Management, College of Plant Protection, China Agricultural University, Beijing, China.
Front Plant Sci. 2021 Sep 8;12:723636. doi: 10.3389/fpls.2021.723636. eCollection 2021.
causes the rice blast, which is one of the most devastating crop diseases worldwide, and is a model fungal pathogen widely used for dissecting the molecular mechanisms underlying fungal virulence/pathogenicity. Although the whole genome sequence of is publicly available, its current transcriptomes remain incomplete, lacking the information on non-protein coding genes and alternative splicing. Here, we performed and analyzed RNA-Seq of conidia and hyphae, resulting in the identification of 3,374 novel genes. Interestingly, the vast majority of these novel genes likely transcribed long non-coding RNAs (lncRNAs), and most of them were localized in the intergenic regions. Notably, their expressions were concomitant with the transcription of neighboring genes thereof in conidia and hyphae. In addition, 2,358 genes were found to undergo alternative splicing events. Furthermore, we exemplified that a lncRNA was important for hyphal growth likely by regulating the neighboring protein-coding gene and that alternative splicing of the transcription factor gene was required for appressorium formation. In summary, results from this study indicate that lncRNA transcripts and alternative splicing events are two important mechanisms for regulating the expression of genes important for conidiation, hyphal growth, and pathogenesis, and provide new insights into transcriptomes and gene regulation in the rice blast fungus.
引发稻瘟病,这是全球最具毁灭性的作物病害之一,并且是一种广泛用于剖析真菌毒力/致病性潜在分子机制的模式真菌病原体。尽管其全基因组序列已公开可用,但其当前转录组仍不完整,缺乏关于非蛋白质编码基因和可变剪接的信息。在此,我们对分生孢子和菌丝进行了RNA测序并分析,结果鉴定出3374个新基因。有趣的是,这些新基因中的绝大多数可能转录长链非编码RNA(lncRNA),并且它们中的大多数位于基因间区域。值得注意的是,它们的表达与分生孢子和菌丝中其相邻基因的转录同时发生。此外,发现2358个基因发生可变剪接事件。此外,我们举例说明一个lncRNA可能通过调节相邻的蛋白质编码基因对菌丝生长很重要,并且转录因子基因的可变剪接是附着胞形成所必需的。总之,本研究结果表明lncRNA转录本和可变剪接事件是调节对分生孢子形成、菌丝生长和致病作用重要的基因表达的两个重要机制,并为稻瘟病菌的转录组和基因调控提供了新的见解。