生长素触发大麦冠根形成过程中基因表达的时间调控:一种综合方法。

IF 4 2区 生物学 Q2 CELL BIOLOGY
Nikola Kořínková, Alexie Techer, Maria Majeská Čudejková, Dieu Thu Nguyen, David Kopečný, Bruno Contreras-Moreira, Pavla Navrátilová, Pascal Gantet, Véronique Bergougnoux
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引用次数: 0

摘要

谷类植物具有纤维根系统,其中冠根是主要组成部分。冠根胚后从茎基部的下部,大部分在地下的节发育。基因表达的严格时空调控控制着这一过程。控制冠根形成(CRI)和发育的信号通路的大部分知识来自水稻。然而,其他谷物可能进化出不同的调节机制,以适应不同的栖息地。本研究利用冠根诱导系统(CRIS)研究大麦CRI的早期分子调控。我们揭示了生长素刺激后24小时内的动态转录组变化。在差异表达基因中,我们从其他谷物中鉴定出了重要的CRI调控基因的同源物,表明CRIS适合于发现与CRI相关的基因。此外,ATAC-seq显示,CRI依赖于根发育相关基因附近和远端基因间区域内染色质可及性的变化。最后,我们重点研究了两个转录因子,HvNAC013和CBF12C,它们可能在CRI和非生物胁迫中都起作用。通过执行DAP-seq,我们确定了它们全基因组的结合位点,并确定了它们潜在的下游靶点。数据表明CBF12C和其他与CRI相关的生长素应答基因可能是HvNAC013的靶点。我们提出HvNAC013和CBF12C作为参与CRI的转录因子网络的一部分,并可能调节根结构以响应环境条件。本研究增加了我们对大麦CRI机制的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Temporal regulation of gene expression during auxin-triggered crown root formation in barley: an integrated approach.

Cereal plants possess a fibrous root system in which crown roots form the major component. Crown roots develop post-embryonically from the lower, mostly underground nodes of the stem base. A strict spatiotemporal regulation of gene expression governs this process. Much of the knowledge about signaling pathways controlling crown root initiation (CRI) and development comes from rice. However, distinct regulatory mechanisms may have evolved in other cereals to adapt to different habitats. In this study, using a Crown Root Inducible System (CRIS), we aimed to investigate the early molecular regulation of barley CRI. We revealed dynamic transcriptomic changes within the first 24 hours following auxin stimulation. Among the differentially expressed genes, we identified orthologs of important CRI regulators from other cereals, demonstrating that CRIS is suitable for uncovering genes involved in CRI. Further, ATAC-seq revealed that CRI relies on changes in chromatin accessibility near root development-related genes and within distal intergenic regions. Finally, we focused on two transcription factors, HvNAC013 and CBF12C, which likely play roles in both CRI and abiotic stresses. By performing DAP-seq, we determined their genome-wide binding sites and identified their potential downstream targets. Data suggest that CBF12C is a putative target of HvNAC013, along with other auxin-responsive genes implicated in CRI. We propose that HvNAC013 and CBF12C function as part of a transcription factor network involved in CRI and potentially modulate root architecture in response to environmental conditions. This study enhances our understanding of the CRI mechanism in barley.

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来源期刊
Plant and Cell Physiology
Plant and Cell Physiology 生物-细胞生物学
CiteScore
8.40
自引率
4.10%
发文量
166
审稿时长
1.7 months
期刊介绍: Plant & Cell Physiology (PCP) was established in 1959 and is the official journal of the Japanese Society of Plant Physiologists (JSPP). The title reflects the journal''s original interest and scope to encompass research not just at the whole-organism level but also at the cellular and subcellular levels. Amongst the broad range of topics covered by this international journal, readers will find the very best original research on plant physiology, biochemistry, cell biology, molecular genetics, epigenetics, biotechnology, bioinformatics and –omics; as well as how plants respond to and interact with their environment (abiotic and biotic factors), and the biology of photosynthetic microorganisms.
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