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首页> 外文期刊>BMC Plant Biology >Differential co-expression networks of long non-coding RNAs and mRNAs in Cleistogenes songorica under water stress and during recovery
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Differential co-expression networks of long non-coding RNAs and mRNAs in Cleistogenes songorica under water stress and during recovery

机译:在水分压力和恢复期间,在Songorica和康复期间在Songorica的长期非编码RNA和MRNA的差分共表达网络

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Water stress seriously constrains plant growth and yield. Long non-coding RNAs (lncRNAs) serve as versatile regulators in various biological regulatory processes. To date, the systematic screening and potential functions of lncRNA have not yet been characterized in Cleistogenes songorica, especially under water stress conditions. In this study, we obtained the root and shoot transcriptomes of young C. songorica plants subjected to different degrees of water stress and recovery treatments by Illumina-based RNA-seq. A total of 3397 lncRNAs were identified through bioinformatics analysis. LncRNA differential expression analysis indicated that?the higher response of roots compared to shoots during water stress and recovery. We further identified the 1644 transcription factors, 189 of which were corresponded to 163 lncRNAs in C. songorica. Though comparative analyses with major Poaceae species based on blast, 81 water stress-related orthologues regulated to lncRNAs were identified as a core of evolutionary conserved genes important to regulate water stress responses in the family. Among these target genes, two genes were found to be involved in the abscisic acid (ABA) signalling pathway, and four genes were enriched for starch and sucrose metabolism. Additionally, the 52 lncRNAs were predicted as target mimics for microRNAs (miRNAs) in C. songorica. RT-qPCR results suggested that MSTRG.43964.1 and MSTRG.4400.2 may regulate the expression of miRNA397 and miRNA166, respectively, as target mimics under water stress and during recovery. Finally, a co-expression network was constructed based on the lncRNAs, miRNAs, protein-coding genes (PCgenes) and transcription factors under water stress and during recovery in C. songorica. In C. songorica, lncRNAs, miRNAs, PCgenes and transcription factors constitute a complex transcriptional regulatory network which lncRNAs can regulate PCgenes and miRNAs under water stress and recovery. This study provides fundamental resources to deepen our knowledge on lncRNAs during ubiquitous water stress.
机译:水压力严重限制了植物生长和产量。长期非编码RNA(LNCRNA)用作各种生物监管过程中的多功能调节剂。迄今为止,LNCRNA的系统筛查和潜在功能尚未以奇咯苷省尚未以水胁迫条件为特征。在这项研究中,我们获得了基于Illumina的RNA-SEQ的不同水分胁迫和恢复治疗的幼小C.松蒿的根和芽转录om。通过生物信息学分析鉴定了总共3397克朗。 LNCRNA差异表达分析表明?在水胁迫和恢复过程中,根部的响应较高。我们进一步确定了1644个转录因子,其中189个与C. Songorica的163克朗。虽然基于Blast的主要淘性物种的比较分析,但对LNCRNA调节的81种与LNCrNA有关的核科学算法被确定为进化保守基因的核心,以调节家庭中的水分应激反应。在这些靶基因中,发现两个基因参与脱离酸(ABA)信号通路,并富含四种基因用于淀粉和蔗糖代谢。另外,预测52个LNCRNA作为C. Songorica中的MicroRNA(miRNA)的靶模模拟物。 RT-QPCR结果表明,MSTRG.43964.1和MSTRG.4400.2可以分别调节miRNA397和miRNA166的表达,作为水胁迫下的靶模模拟和在恢复过程中。最后,基于LNCRNA,MiRNA,蛋白质编码基因(PCGENES)和水分应激的转录因子和转录因子和在C. Songorica的回收期间构建了共表达网络。在C. Songorica,LNCRNA,MIRNA,PCGENES和转录因子中构成了一种复杂的转录调节网络,LNCRNA可以在水胁迫下调节PCGENES和MIRNA。本研究提供了基本资源,以加深在普遍存在的水分压力期间对LNCRNA的了解。

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