Chromatin accessibility dynamics and transcriptional regulatory networks underlying the primary nitrogen response in rice roots.

IF 9.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Plant Communications Pub Date : 2025-07-14 Epub Date: 2025-06-03 DOI:10.1016/j.xplc.2025.101392
Wenhui Li, Xinxin Zhu, Junjiao Yang, Xiangyu Zhou, Luchang Ming, Ling Yang, Jiacheng Li, Zengdong Tan, Chunjiao Xia, Dujun Wang, Xingbing Xu, Zhanxiang Zong, Hu Zhao, Meng Yang, Lizhong Xiong, Xingming Lian, Weibo Xie
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Abstract

Nitrogen (N) is essential for rice growth; however, the transcriptional regulation of the primary nitrogen response (PNR), characterized by the rapid upregulation of N uptake and assimilation genes upon N resupply, remains poorly understood. This study investigated the dynamics of the PNR in the roots of two rice cultivars (Zhenshan 97 and Nipponbare) via time-series Assay for Transposase-Accessible Chromatin using sequencing and RNA sequencing analyses within 2 h of ammonium nitrate resupply. Regulatory regions responsive to N induction were precisely identified. Coordinated and cascading changes in chromatin accessibility and gene expression were observed, with chromatin state frequently preceding transcriptional changes. Integrative analysis of expression-chromatin accessibility associations revealed a redundant N-responsive regulatory network. OsLBD38 and OsLBD39, identified as early-response regulators, transcriptionally suppress nitrate reductases while enhancing nitrite reductases; they may function as metabolic safeguarders to prevent nitrite accumulation. OsbZIP23 was identified as a novel regulator directly binding to the promoters of N uptake and metabolism genes, regulating genes in patterns opposite to LBD-regulated genes, suggesting a complex regulatory interplay. Cross-species comparisons with Arabidopsis highlighted the conserved N-responsive regulatory roles of these hub regulators and their targets. Comparative analyses between cultivars revealed expression divergence and genetic differentiation in N-responsive genes, implying indica/japonica-specific adaptations. Furthermore, deep learning predictions of chromatin accessibility between cultivars indicated that expression variation in N uptake and metabolism genes is primarily influenced by trans-acting regulatory factors. These findings provide a comprehensive view of the dynamic regulatory landscape governing the PNR in rice.

水稻根系初级氮素响应背后的染色质可及性动态和转录调控网络。
氮(N)对水稻生长至关重要,但对初级氮素响应(PNR)的转录调控尚不清楚,其特征是氮素吸收和同化基因在氮素再补给时的快速上调。本研究利用ATAC-seq和RNA-seq分析了两个水稻品种(珍汕97和日本裸稻)在硝酸铵补充后2 h内根系PNR的动态变化,并精确鉴定了对氮诱导响应的调控区域。我们观察到染色质可及性和基因表达的协调和级联变化,染色质状态通常先于转录变化。表达-染色质可及性关联的综合分析揭示了一个冗余的n响应调节网络。作为早期反应调节因子,OsLBD38和OsLBD39转录抑制硝酸盐还原酶,同时增强亚硝酸盐还原酶,可能作为代谢保护因子防止亚硝酸盐积累。OsbZIP23是一种新型的直接结合氮摄取/代谢基因启动子的调控因子,其调控方式与lbd调控基因相反,表明其调控相互作用复杂。与拟南芥的跨物种比较突出了这些枢纽调节因子及其靶点的保守的n响应调节作用。品种间的比较分析揭示了氮响应基因的表达差异和遗传分化,表明存在亚种特异性适应。此外,品种间染色质可及性的深度学习预测表明,氮吸收/代谢基因的表达差异主要受反式调控因子的影响。总之,我们的研究为水稻PNR的动态调控格局提供了一个全面的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Plant Communications
Plant Communications Agricultural and Biological Sciences-Plant Science
CiteScore
15.70
自引率
5.70%
发文量
105
审稿时长
6 weeks
期刊介绍: Plant Communications is an open access publishing platform that supports the global plant science community. It publishes original research, review articles, technical advances, and research resources in various areas of plant sciences. The scope of topics includes evolution, ecology, physiology, biochemistry, development, reproduction, metabolism, molecular and cellular biology, genetics, genomics, environmental interactions, biotechnology, breeding of higher and lower plants, and their interactions with other organisms. The goal of Plant Communications is to provide a high-quality platform for the dissemination of plant science research.
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