Dong Jiang, Lai Wei, Li-Jun Huang, Xia Peng, Chuantong Cui, Yakov Kuzyakov, Ning Li
{"title":"A multi-tissue single-cell atlas of moso bamboo (Phyllostachys edulis) reveals cellular heterogeneity and lineage trajectories.","authors":"Dong Jiang, Lai Wei, Li-Jun Huang, Xia Peng, Chuantong Cui, Yakov Kuzyakov, Ning Li","doi":"10.1093/treephys/tpag086","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":23286,"journal":{"name":"Tree physiology","volume":" ","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tree physiology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1093/treephys/tpag086","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FORESTRY","Score":null,"Total":0}
引用次数: 0
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.
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.