A multi-tissue single-cell atlas of moso bamboo (Phyllostachys edulis) reveals cellular heterogeneity and lineage trajectories.

IF 4 2区 农林科学 Q1 FORESTRY
Dong Jiang, Lai Wei, Li-Jun Huang, Xia Peng, Chuantong Cui, Yakov Kuzyakov, Ning Li
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Abstract

Moso bamboo (Phyllostachys edulis) is a high-value renewable resource used for timber, fiber and carbon sequestration, yet the cellular basis of its development remains poorly resolved. Here, we performed a systematic single-cell RNA-sequencing analysis of moso bamboo seedlings, generating 31,658 high-quality single-cell transcriptomes. Initial unsupervised graph-based clustering partitioned the dataset into 23 clusters, which were subsequently assigned to 11 major cell-type categories through marker-guided and biologically informed annotation, including meristemoid, coleoptile L1 epidermis, cortex, epidermis, mesophyll precursor, mestome sheath, pericycle, phloem, endodermis, root cap and xylem. Pseudo-time analysis suggested putative vascular-associated trajectories in which captured xylem and phloem cells were ordered along a bifurcating structure extending from meristem populations. Xylem cells were enriched in cell wall modification genes, while phloem cells preferentially expressed transport- and defense-related genes. Root cell differentiation exhibited polar patterning, progressing through seven stages from meristems to epidermis, endodermis, cortex and root cap lineages. Leaf development followed a unidirectional trajectory from meristems to mestome sheath cells and coleoptile L1 epidermis, and ultimately to mesophyll cells. We further identified key regulatory factors underlying these cellular differentiations, revealing developmental path differences among roots, stems and leaves. This study constructs a high-resolution cellular atlas of moso bamboo seedlings that delineates developmental programs underlying rapid growth and environmental adaptation, and uncovers dynamic trajectories from meristems to specialized cell types. These findings provide candidate regulators for future genetic studies to enhance biomass production and stress tolerance in moso bamboo.

毛竹(Phyllostachys edulis)多组织单细胞图谱揭示了毛竹的细胞异质性和谱系轨迹。
毛竹(Phyllostachys edulis)是一种高价值的可再生资源,用于木材、纤维和碳封存,但其发育的细胞基础仍未得到很好的解决。在这里,我们对毛竹幼苗进行了系统的单细胞rna测序(scRNA-seq)分析,产生了31,658个高质量的单细胞转录组。最初基于无监督图的聚类将数据集划分为23个簇,随后通过标记引导和生物学信息注释将其划分为11个主要的细胞类型类别,包括分生组织、胚芽L1表皮、皮层、表皮、叶肉前体、间质鞘、中柱鞘、韧皮部、内胚层、根冠和木质部。伪时间分析表明,在维管相关的轨迹中,捕获的木质部和韧皮部细胞沿着分生组织群体延伸的分叉结构排列。木质部细胞富集细胞壁修饰基因,韧皮部细胞优先表达运输和防御相关基因。根细胞分化表现为极性模式,从分生组织到表皮、内胚层、皮层和根冠谱系经历了7个阶段。叶片发育遵循从分生组织到中间鞘细胞、胚芽组织L1表皮、最终到叶肉细胞的单向发展轨迹。我们进一步确定了这些细胞分化背后的关键调控因子,揭示了根、茎和叶之间的发育路径差异。本研究构建了毛竹幼苗的高分辨率细胞图谱,描绘了毛竹幼苗快速生长和环境适应的发育过程,揭示了毛竹幼苗从分生组织到特化细胞类型的动态轨迹。这些发现为未来的遗传研究提供了候选调控因子,以提高毛竹的生物量产量和抗逆性。
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来源期刊
Tree physiology
Tree physiology 农林科学-林学
CiteScore
7.10
自引率
7.50%
发文量
133
审稿时长
1 months
期刊介绍: Tree Physiology promotes research in a framework of hierarchically organized systems, measuring insight by the ability to link adjacent layers: thus, investigated tree physiology phenomenon should seek mechanistic explanation in finer-scale phenomena as well as seek significance in larger scale phenomena (Passioura 1979). A phenomenon not linked downscale is merely descriptive; an observation not linked upscale, might be trivial. Physiologists often refer qualitatively to processes at finer or coarser scale than the scale of their observation, and studies formally directed at three, or even two adjacent scales are rare. To emphasize the importance of relating mechanisms to coarser scale function, Tree Physiology will highlight papers doing so particularly well as feature papers.
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