Haidong Yan,John P Mendieta,Xuan Zhang,Ziliang Luo,Alexandre P Marand,Yan Liang,Mark A A Minow,Yun Zhong,Yarong Jin,Hosung Jang,Xiang Li,Xinxin Zhang,Thomas Roulé,Doris Wagner,Xiaoyu Tu,Yonghong Wang,Daiquan Jiang,Silin Zhong,Linkai Huang,Susan R Wessler,Robert J Schmitz
{"title":"单细胞水稻图谱整合了多物种数据,揭示了顺式调控进化。","authors":"Haidong Yan,John P Mendieta,Xuan Zhang,Ziliang Luo,Alexandre P Marand,Yan Liang,Mark A A Minow,Yun Zhong,Yarong Jin,Hosung Jang,Xiang Li,Xinxin Zhang,Thomas Roulé,Doris Wagner,Xiaoyu Tu,Yonghong Wang,Daiquan Jiang,Silin Zhong,Linkai Huang,Susan R Wessler,Robert J Schmitz","doi":"10.1038/s41477-025-02106-6","DOIUrl":null,"url":null,"abstract":"Cis-regulatory elements (CREs) are essential for regulating gene expression, yet their evolutionary dynamics in plants remain elusive. Here we constructed a single-cell chromatin accessibility atlas for Oryza sativa from 103,911 nuclei representing 126 cell states across nine organs. Comparative genomics between O. sativa and 57,552 nuclei from four additional grass species (Zea mays, Sorghum bicolor, Panicum miliaceum and Urochloa fusca) revealed that chromatin accessibility conservation varies with cell-type specificity. Epidermal accessible chromatin regions in the leaf were less conserved compared to other cell types, indicating accelerated regulatory evolution in the L1-derived epidermal layer of O. sativa relative to other species. Conserved accessible chromatin regions overlapping the repressive histone modification H3K27me3 were identified as potentially silencer-like CREs, as deleting these regions led to up-regulation of gene expression. This study provides a comprehensive epigenomic resource for the rice community, demonstrating the utility of a comparative genomics approach that highlights the dynamics of plant cell-type-specific CRE evolution.","PeriodicalId":18904,"journal":{"name":"Nature Plants","volume":"8 1","pages":""},"PeriodicalIF":13.6000,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A single-cell rice atlas integrates multi-species data to reveal cis-regulatory evolution.\",\"authors\":\"Haidong Yan,John P Mendieta,Xuan Zhang,Ziliang Luo,Alexandre P Marand,Yan Liang,Mark A A Minow,Yun Zhong,Yarong Jin,Hosung Jang,Xiang Li,Xinxin Zhang,Thomas Roulé,Doris Wagner,Xiaoyu Tu,Yonghong Wang,Daiquan Jiang,Silin Zhong,Linkai Huang,Susan R Wessler,Robert J Schmitz\",\"doi\":\"10.1038/s41477-025-02106-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Cis-regulatory elements (CREs) are essential for regulating gene expression, yet their evolutionary dynamics in plants remain elusive. Here we constructed a single-cell chromatin accessibility atlas for Oryza sativa from 103,911 nuclei representing 126 cell states across nine organs. Comparative genomics between O. sativa and 57,552 nuclei from four additional grass species (Zea mays, Sorghum bicolor, Panicum miliaceum and Urochloa fusca) revealed that chromatin accessibility conservation varies with cell-type specificity. Epidermal accessible chromatin regions in the leaf were less conserved compared to other cell types, indicating accelerated regulatory evolution in the L1-derived epidermal layer of O. sativa relative to other species. Conserved accessible chromatin regions overlapping the repressive histone modification H3K27me3 were identified as potentially silencer-like CREs, as deleting these regions led to up-regulation of gene expression. This study provides a comprehensive epigenomic resource for the rice community, demonstrating the utility of a comparative genomics approach that highlights the dynamics of plant cell-type-specific CRE evolution.\",\"PeriodicalId\":18904,\"journal\":{\"name\":\"Nature Plants\",\"volume\":\"8 1\",\"pages\":\"\"},\"PeriodicalIF\":13.6000,\"publicationDate\":\"2025-09-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Plants\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1038/s41477-025-02106-6\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Plants","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41477-025-02106-6","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
A single-cell rice atlas integrates multi-species data to reveal cis-regulatory evolution.
Cis-regulatory elements (CREs) are essential for regulating gene expression, yet their evolutionary dynamics in plants remain elusive. Here we constructed a single-cell chromatin accessibility atlas for Oryza sativa from 103,911 nuclei representing 126 cell states across nine organs. Comparative genomics between O. sativa and 57,552 nuclei from four additional grass species (Zea mays, Sorghum bicolor, Panicum miliaceum and Urochloa fusca) revealed that chromatin accessibility conservation varies with cell-type specificity. Epidermal accessible chromatin regions in the leaf were less conserved compared to other cell types, indicating accelerated regulatory evolution in the L1-derived epidermal layer of O. sativa relative to other species. Conserved accessible chromatin regions overlapping the repressive histone modification H3K27me3 were identified as potentially silencer-like CREs, as deleting these regions led to up-regulation of gene expression. This study provides a comprehensive epigenomic resource for the rice community, demonstrating the utility of a comparative genomics approach that highlights the dynamics of plant cell-type-specific CRE evolution.
期刊介绍:
Nature Plants is an online-only, monthly journal publishing the best research on plants — from their evolution, development, metabolism and environmental interactions to their societal significance.