Jia Jinbu, Lu Wenqin, Zhong Chengcheng, Zhou Ran, Xu Junjie, Liu Wei, Gou Xiuhong, Wang Qinhu, Yin Junliang, Xu Cheng, Shan Weixing
State Key Laboratory of Crop Stress Biology for Arid Areas and College of Plant Protection, Northwest A&F UniversityYangling, China.
Chongqing Tobacco Research InstituteChongqing, China.
Front Microbiol. 2017 May 2;8:773. doi: 10.3389/fmicb.2017.00773. eCollection 2017.
Small RNAs (sRNAs) are important non-coding RNA regulators, playing key roles in developmental regulation, transposon suppression, environmental response, host-pathogen interaction and other diverse biological processes. However, their roles in oomycetes are poorly understood. Here, we performed sRNA sequencing and RNA sequencing of at stages of vegetative growth and infection of roots to examine diversity and function of sRNAs in , a model hemibiotrophic oomycete plant pathogen. Our results indicate that there are two distinct types of sRNA-generating loci in genome, giving rise to clusters of 25-26 nt and 21 nt sRNAs, respectively, with no significant strand-biases. The 25-26 nt sRNA loci lie predominantly in gene-sparse and repeat-rich regions, and overlap with over 7000 endogenous gene loci. These overlapped genes are typically species-specific, with no homologies to the sister species . They include approximately 40% RXLR effector genes, 50% CRN effector genes and some elicitor genes. The transcripts of most of these genes could not be detected at both the vegetative mycelium and infection stages as revealed by RNA sequencing, indicating that the 25-26 nt sRNAs are associated with efficient silencing of these genes. The 21 nt sRNA loci typically overlap with the exon regions of highly expressed genes, suggesting that the biogenesis of the 21 nt sRNAs may be dependent on the level of gene transcription and that these sRNAs do not mediate efficient silencing of homologous genes. Analyses of the published sRNA and mRNA sequencing data consistently show that the 25-26 nt sRNAs, but not the 21 nt sRNAs, may mediate efficient gene silencing in .
小RNA(sRNA)是重要的非编码RNA调控因子,在发育调控、转座子抑制、环境响应、宿主-病原体相互作用及其他多种生物学过程中发挥关键作用。然而,它们在卵菌中的作用却鲜为人知。在此,我们对一种典型的半活体营养型卵菌植物病原体——致病疫霉在营养生长和侵染根部阶段进行了sRNA测序和RNA测序,以研究sRNA在致病疫霉中的多样性和功能。我们的结果表明,致病疫霉基因组中存在两种不同类型的sRNA产生位点,分别产生25 - 26 nt和21 nt的sRNA簇,且无明显的链偏好性。25 - 26 nt的sRNA位点主要位于基因稀疏和富含重复序列的区域,并与7000多个内源性基因位点重叠。这些重叠基因通常是致病疫霉物种特有的,与姊妹物种寄生疫霉没有同源性。它们包括约40%的RXLR效应蛋白基因、50%的CRN效应蛋白基因和一些激发子基因。RNA测序显示,在营养菌丝体和侵染阶段均未检测到这些基因中的大多数转录本,这表明25 - 26 nt的sRNA与这些基因的有效沉默相关。21 nt的sRNA位点通常与高表达基因的外显子区域重叠,这表明21 nt sRNA的生物合成可能依赖于基因转录水平,且这些sRNA不介导同源基因的有效沉默。对已发表的致病疫霉sRNA和mRNA测序数据的分析一致表明,25 - 26 nt的sRNA而非21 nt的sRNA可能介导致病疫霉中的有效基因沉默。