时空转录组图谱揭示竹笋快速生长器官形成过程中的基因调控模式

IF 9.4 1区 生物学 Q1 Agricultural and Biological Sciences New Phytologist Pub Date : 2024-08-14 DOI:10.1111/nph.20059
Jing Guo, Dan Luo, Yamao Chen, Fengjiao Li, Jiajia Gong, Fen Yu, Wengen Zhang, Ji Qi, Chunce Guo
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引用次数: 0

摘要

竹子以其惊人的生长速度和经济意义,为研究快速生长植物器官发生的分子基础提供了一个理想的系统,尤其是在单子叶植物中,关于笋尖和闰分生组织的维持和分化的基因调控网络仍然是一个有争议的主题。我们在 10× 平台上采用了空间和单核转录组测序技术,精确剖析了竹笋不同组织和早期发育阶段的基因功能。我们的综合分析揭示了笋发育过程中独特的细胞轨迹,发现了参与原鳞茎分化、闰分生组织形成和维管组织发育的关键基因和通路。关键调控基因的空间和时间表达模式,特别是与激素信号转导和脂质代谢相关的基因,有力地支持了髓间分生组织起源于被包围的实质细胞的假说。髓间分生组织中特定基因的表达呈现有规律的分散分布模式,为了解驱动竹笋快速生长的复杂分子机制提供了线索。单个细胞核和空间转录组分析揭示了基因活动的全貌,加深了对器官发生的分子结构的理解,并为未来依赖特定细胞类型身份的基因组和遗传学研究提供了宝贵的资源。
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Spatiotemporal transcriptome atlas reveals gene regulatory patterns during the organogenesis of the rapid growing bamboo shoots.

Bamboo with its remarkable growth rate and economic significance, offers an ideal system to investigate the molecular basis of organogenesis in rapidly growing plants, particular in monocots, where gene regulatory networks governing the maintenance and differentiation of shoot apical and intercalary meristems remain a subject of controversy. We employed both spatial and single-nucleus transcriptome sequencing on 10× platform to precisely dissect the gene functions in various tissues and early developmental stages of bamboo shoots. Our comprehensive analysis reveals distinct cell trajectories during shoot development, uncovering critical genes and pathways involved in procambium differentiation, intercalary meristem formation, and vascular tissue development. Spatial and temporal expression patterns of key regulatory genes, particularly those related to hormone signaling and lipid metabolism, strongly support the hypothesis that intercalary meristem origin from surrounded parenchyma cells. Specific gene expressions in intercalary meristem exhibit regular and dispersed distribution pattern, offering clues for understanding the intricate molecular mechanisms that drive the rapid growth of bamboo shoots. The single-nucleus and spatial transcriptome analysis reveal a comprehensive landscape of gene activity, enhancing the understanding of the molecular architecture of organogenesis and providing valuable resources for future genomic and genetic studies relying on identities of specific cell types.

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来源期刊
New Phytologist
New Phytologist PLANT SCIENCES-
CiteScore
17.60
自引率
5.30%
发文量
728
审稿时长
1 months
期刊介绍: New Phytologist is a leading publication that showcases exceptional and groundbreaking research in plant science and its practical applications. With a focus on five distinct sections - Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology - the journal covers a wide array of topics ranging from cellular processes to the impact of global environmental changes. We encourage the use of interdisciplinary approaches, and our content is structured to reflect this. Our journal acknowledges the diverse techniques employed in plant science, including molecular and cell biology, functional genomics, modeling, and system-based approaches, across various subfields.
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