冷诱导的lncrna SVALKA和SVALNA的顺式和反式作用调节拟南芥CBF1和CBF3。

IF 6.2 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Isabell Rosenkranz, Sarah Mermet, Vasiliki Zacharaki, Peter Kindgren
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引用次数: 0

摘要

长链非编码rna (lncRNAs)正成为真核生物编码基因表达的关键调控分子。在此,我们研究了冷胁迫条件下拟南芥中lncrna SVALKA (SVK)和SVALNA (SVN)在调节CBF1和CBF3基因表达中的作用。我们将组学方法与遗传学和分子生物学相结合,揭示了SVK和SVN的转录动力学和调控机制。我们的研究结果表明,SVK作为顺式和反式lncRNA,通过RNAPII碰撞和染色质重塑调节CBF1和CBF3,而SVN通过RNAPII碰撞机制负向调节CBF3,发挥顺式作用。我们确定了SVK的同工型,它们起源于不同的转录起始位点,并经历了选择性剪接,这可能对适应稳定性很重要,对调节功能至关重要。此外,我们发现两个位置保守的lncrna,源自邻近基因的上游反义链,可以有不同的分子机制来调节它们的靶标。本研究阐明了lncrna在基因调控中的复杂相互作用,强调了它们在调节对环境胁迫的反应中的重要作用。我们的发现有助于更深入地了解lncRNA功能的机制及其在真核生物基因调控网络中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cis- and trans-action of the cold-induced lncRNAs, SVALKA and SVALNA, regulate CBF1 and CBF3 in Arabidopsis.

Long noncoding RNAs (lncRNAs) are emerging as key regulatory players of coding gene expression in eukaryotes. Here, we investigate the roles of the lncRNAs SVALKA (SVK) and SVALNA (SVN) in regulating CBF1 and CBF3 gene expression in Arabidopsis under cold stress conditions. We integrated omics approaches, together with genetics and molecular biology, to uncover the transcriptional dynamics and regulatory mechanisms of SVK and SVN. Our results demonstrate that SVK functions as a cis- and trans-acting lncRNA, regulating both CBF1 and CBF3 through RNAPII collision and chromatin remodeling, while SVN serves a cis role by negatively regulating CBF3 via a RNAPII collision mechanism. We identified isoforms of SVK, originating from distinct transcription start sites and undergo alternative splicing which might be important to adapt stability, crucial for the regulatory functions. Furthermore, we show that two positionally conserved lncRNAs, originating from the upstream antisense strand of neighboring genes, can have different molecular mechanisms to regulate their targets. This study elucidates the complex interplay of lncRNAs in gene regulation, highlighting their essential roles in modulating responses to environmental stresses. Our findings contribute to a deeper understanding of the mechanisms underlying lncRNA functionality and their significance in gene regulatory networks in eukaryotes.

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来源期刊
EMBO Reports
EMBO Reports 生物-生化与分子生物学
CiteScore
11.20
自引率
1.30%
发文量
267
审稿时长
1 months
期刊介绍: EMBO Reports is a scientific journal that specializes in publishing research articles in the fields of molecular biology, cell biology, and developmental biology. The journal is known for its commitment to publishing high-quality, impactful research that provides novel physiological and functional insights. These insights are expected to be supported by robust evidence, with independent lines of inquiry validating the findings. The journal's scope includes both long and short-format papers, catering to different types of research contributions. It values studies that: Communicate major findings: Articles that report significant discoveries or advancements in the understanding of biological processes at the molecular, cellular, and developmental levels. Confirm important findings: Research that validates or supports existing knowledge in the field, reinforcing the reliability of previous studies. Refute prominent claims: Studies that challenge or disprove widely accepted ideas or hypotheses in the biosciences, contributing to the correction and evolution of scientific understanding. Present null data: Papers that report negative results or findings that do not support a particular hypothesis, which are crucial for the scientific process as they help to refine or redirect research efforts. EMBO Reports is dedicated to maintaining high standards of scientific rigor and integrity, ensuring that the research it publishes contributes meaningfully to the advancement of knowledge in the life sciences. By covering a broad spectrum of topics and encouraging the publication of both positive and negative results, the journal plays a vital role in promoting a comprehensive and balanced view of scientific inquiry. 
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