Xia Shi-Wei, Song Chang-Jiang, Zheng Xiao-Fang, Zhang Yuan, Anwar Wajid, Dissanayaka Dissanayakalage D N V, Zhu Ping-Zhi, Liu Jun-Li, Lai Yun-Song
College of Horticulture, Sichuan Agricultural University, Chengdu, 611130, China.
BMC Plant Biol. 2025 Jun 3;25(1):748. doi: 10.1186/s12870-025-06752-y.
The cucumber (Cucumis sativus) is a model species for genomic studies in vegetables due to its relatively small genome size. Long non-coding RNAs (lncRNAs) play crucial roles in plant growth, development, and stress responses. LncRNAs are less conserved among plant species and comparative genomic study of lncRNA in cucumbers can provide new insight about the evolution and function of cucumber lncRNAs.
Here, full-length transcriptome sequencing was applied to identify high-confidence lncRNAs in wild (C. sativus var. hardwickii) and semi-wild (C. sativus var. xishuangbannanensis) cucumbers. A total of 1,598 lncRNAs were screened out, and these lncRNAs exhibit distinct characteristics, including fewer exons, shorter sequences, and lower GC content when compared with messenger RNAs (mRNAs). We observed a slight expansion of lncRNAs, such as lncRNA family 1, which could contain up to 21 members distributed across different chromosomes. These family members are typically derived from the same genomic region, likely as a result of alternative splicing. Differentially expressed lncRNAs (DELs) may cis-regulate the expression of nearby genes, and functional enrichment analysis indicated that the primary biological process involved was environmental adaptation. We predicted that eighteen lncRNAs could serve as microRNA (miRNA) precursors, generating 25 miRNAs, which subsequently target 1,628 protein-coding genes. Functional enrichment analysis revealed that these target genes were primarily enriched in epigenetic regulatory pathways, suggesting a complex feedback regulation involving epigenetic modifications and gene expression. The competing endogenous RNA (ceRNA) network analysis revealed that 31 lncRNAs interacted with 26 miRNAs and competed for 134 targeted protein-coding genes. MiR156 plays a crucial role in the ceRNA network, competing with CsLncRNA94 to target the 7 members of the SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) transcription factor gene family. We observed that CsLncRNA94 participates in the miR156-SPL module's response to light and low temperature and acts as a negative regulator of cold tolerance in cucumber, as demonstrated through transient expression in cotyledons.
Full-length lncRNAs were identified in wild- and semi-wild cucumbers. The differential expression of lncRNAs between cucumbers with different domestication degree is likely for environmental adaptation particularly via lncRNA-miRNA pathway. CsLncRNA94 is a representative lncRNA that regulate miR156-SPL module in response to light and temperature stimuli.
Not applicable.
黄瓜(Cucumis sativus)因其相对较小的基因组大小,是蔬菜基因组研究的模式物种。长链非编码RNA(lncRNAs)在植物生长、发育和应激反应中发挥着关键作用。lncRNAs在植物物种间的保守性较低,对黄瓜lncRNA进行比较基因组研究可以为黄瓜lncRNA的进化和功能提供新的见解。
本文应用全长转录组测序技术,在野生黄瓜(C. sativus var. hardwickii)和半野生黄瓜(C. sativus var. xishuangbannanensis)中鉴定出高可信度的lncRNAs。共筛选出1598个lncRNAs,这些lncRNAs表现出独特的特征,与信使RNA(mRNAs)相比,其外显子较少、序列较短且GC含量较低。我们观察到lncRNAs有轻微的扩张,如lncRNA家族1,该家族可能包含多达21个成员,分布在不同染色体上。这些家族成员通常来自同一基因组区域,可能是可变剪接的结果。差异表达的lncRNAs(DELs)可能顺式调节附近基因的表达,功能富集分析表明主要涉及环境适应的生物学过程。我们预测18个lncRNAs可以作为微小RNA(miRNA)前体,产生25个miRNAs,这些miRNAs随后靶向1628个蛋白质编码基因。功能富集分析表明,这些靶基因主要富集在表观遗传调控途径中,表明存在涉及表观遗传修饰和基因表达的复杂反馈调节。竞争性内源RNA(ceRNA)网络分析表明,31个lncRNAs与26个miRNAs相互作用,并竞争134个靶向蛋白质编码基因。MiR156在ceRNA网络中起关键作用,与CsLncRNA94竞争,靶向SQUAMOSA启动子结合蛋白样(SPL)转录因子基因家族的7个成员。我们观察到CsLncRNA94参与了miR156-SPL模块对光和低温的反应,并作为黄瓜耐寒性的负调节因子,通过在子叶中的瞬时表达得到证实。
在野生和半野生黄瓜中鉴定出全长lncRNAs。不同驯化程度黄瓜之间lncRNAs的差异表达可能是为了适应环境,特别是通过lncRNA-miRNA途径。CsLncRNA94是一个代表性的lncRNA,可响应光和温度刺激调节miR156-SPL模块。
不适用。