Jo-Wei Allison Hsieh, Pin-Chien Liou, Chia-Chang Lin, Xiufang Dai, Chen-Wei Hu, I-Fan Wang, Jr-Fong Dang, Yi-Chi Ho, Kai-Wen Cheng, Wenjing Xu, Shang-Che Kuo, Chung-Ting Kao, Dian-Xuan Yang, Ray Wang, Ke Xiao, Jeng-Shane Lin, Cheng-Chih Hsu, Chuan-Chih Hsu, Te-Lun Mai, Yuxiang Cheng, Ying-Chung Jimmy Lin
{"title":"单细胞和空间多组学研究了机械胁迫下杨树木质部的异质发育","authors":"Jo-Wei Allison Hsieh, Pin-Chien Liou, Chia-Chang Lin, Xiufang Dai, Chen-Wei Hu, I-Fan Wang, Jr-Fong Dang, Yi-Chi Ho, Kai-Wen Cheng, Wenjing Xu, Shang-Che Kuo, Chung-Ting Kao, Dian-Xuan Yang, Ray Wang, Ke Xiao, Jeng-Shane Lin, Cheng-Chih Hsu, Chuan-Chih Hsu, Te-Lun Mai, Yuxiang Cheng, Ying-Chung Jimmy Lin","doi":"10.1016/j.devcel.2025.06.038","DOIUrl":null,"url":null,"abstract":"Xylem, the predominant tissue for structural support, forms tension wood with G-layer-rich fibers under mechanical stress. Despite being recognized over a century ago, three key biological questions remained unclear: (1) are fibers in normal and tension wood distinct cells due to morphological differences? (2) Do tension wood fibers arise from different lineages? (3) What are the key genes controlling tension wood formation? We conducted single-cell RNA sequencing on normal, tension and opposite xylem. Fibers in normal and tension wood belong to the same cell type and lineage. Differential developmental speed and cell-type ratio in tension and opposite xylem were further validated by spatial transcriptomics and metabolomics. Phosphoproteomics showed mechanical sensing mechanisms conserved between stems and roots across angiosperms. We identified a group of genes involved in the cell fate transition in tension wood. The knowledge on the heterogeneity of cell development offers insights into optimizing biomass production and bioenergy yield.","PeriodicalId":11157,"journal":{"name":"Developmental cell","volume":"94 1","pages":""},"PeriodicalIF":8.7000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Single-cell and spatial multiomics identifies heterogeneous xylem development driven by mechanical stress in Populus\",\"authors\":\"Jo-Wei Allison Hsieh, Pin-Chien Liou, Chia-Chang Lin, Xiufang Dai, Chen-Wei Hu, I-Fan Wang, Jr-Fong Dang, Yi-Chi Ho, Kai-Wen Cheng, Wenjing Xu, Shang-Che Kuo, Chung-Ting Kao, Dian-Xuan Yang, Ray Wang, Ke Xiao, Jeng-Shane Lin, Cheng-Chih Hsu, Chuan-Chih Hsu, Te-Lun Mai, Yuxiang Cheng, Ying-Chung Jimmy Lin\",\"doi\":\"10.1016/j.devcel.2025.06.038\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Xylem, the predominant tissue for structural support, forms tension wood with G-layer-rich fibers under mechanical stress. Despite being recognized over a century ago, three key biological questions remained unclear: (1) are fibers in normal and tension wood distinct cells due to morphological differences? (2) Do tension wood fibers arise from different lineages? (3) What are the key genes controlling tension wood formation? We conducted single-cell RNA sequencing on normal, tension and opposite xylem. Fibers in normal and tension wood belong to the same cell type and lineage. Differential developmental speed and cell-type ratio in tension and opposite xylem were further validated by spatial transcriptomics and metabolomics. Phosphoproteomics showed mechanical sensing mechanisms conserved between stems and roots across angiosperms. We identified a group of genes involved in the cell fate transition in tension wood. The knowledge on the heterogeneity of cell development offers insights into optimizing biomass production and bioenergy yield.\",\"PeriodicalId\":11157,\"journal\":{\"name\":\"Developmental cell\",\"volume\":\"94 1\",\"pages\":\"\"},\"PeriodicalIF\":8.7000,\"publicationDate\":\"2025-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developmental cell\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.devcel.2025.06.038\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.devcel.2025.06.038","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Single-cell and spatial multiomics identifies heterogeneous xylem development driven by mechanical stress in Populus
Xylem, the predominant tissue for structural support, forms tension wood with G-layer-rich fibers under mechanical stress. Despite being recognized over a century ago, three key biological questions remained unclear: (1) are fibers in normal and tension wood distinct cells due to morphological differences? (2) Do tension wood fibers arise from different lineages? (3) What are the key genes controlling tension wood formation? We conducted single-cell RNA sequencing on normal, tension and opposite xylem. Fibers in normal and tension wood belong to the same cell type and lineage. Differential developmental speed and cell-type ratio in tension and opposite xylem were further validated by spatial transcriptomics and metabolomics. Phosphoproteomics showed mechanical sensing mechanisms conserved between stems and roots across angiosperms. We identified a group of genes involved in the cell fate transition in tension wood. The knowledge on the heterogeneity of cell development offers insights into optimizing biomass production and bioenergy yield.
期刊介绍:
Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.