<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li Y</submitter><funding>Development funds of the National Key Laboratory of Crop Genetic Improvement</funding><funding>Hubei Provincial Postdoctoral Innovative Talent Cultivation Program</funding><funding>Fundamental Research Funds for the Central Universities</funding><funding>Hubei Provincial Natural Science Foundation for Young Scholars Project</funding><funding>Hubei Hongshan Laboratory Start Fund</funding><funding>National Natural Science Foundation of China</funding><funding>China Postdoctoral Science Foundation</funding><funding>National Key Research and Development Program of Hubei Province</funding><funding>Biological Breeding-National Science and Technology Major Project</funding><funding>Postdoctoral Fellowship Program of CPSF</funding><funding>Department of Human Resources and Social Security of Hubei Province</funding><pagination>58</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12930761</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Trimethylation of histone H3 lysine 27 (H3K27me3) confers a repressive chromatin state and is dynamically deposited and removed to regulate gene expression throughout plant growth and development. Nevertheless, the three-dimensional epigenome architecture linked to H3K27me3 and its regulatory role in controlling rice development remain unclear.&lt;h4>Results&lt;/h4>Here, we employ long-read ChIA-PET to map the genome topology associated with H3K27me3 in rice, identifying hundreds of repressive chromatin spatial clusters within chromosomes. The T-DNA insertional mutagenesis of EMBRYONIC FLOWER 2b (OsEMF2b) leads to disruption of H3K27me3-associated chromatin interaction networks. Notably, we discover that the three key flowering time loci, Early heading date 1 (Ehd1) and Headin</pubmed_abstract><journal>Genome biology</journal><pubmed_title>3D epigenome architecture orchestrates cis and trans regulation of flowering time in rice.</pubmed_title><pmcid>PMC12930761</pmcid><funding_grant_id>2662024SKPY002, 2662023SKQD002</funding_grant_id><funding_grant_id>2025AFB377</funding_grant_id><funding_grant_id>2023ZD04076</funding_grant_id><funding_grant_id>2022BBA54</funding_grant_id><funding_grant_id>2023HSQD002</funding_grant_id><funding_grant_id>590320103</funding_grant_id><funding_grant_id>2022T150245, 2022M711264</funding_grant_id><funding_grant_id>32470669, 32200424</funding_grant_id><funding_grant_id>WHGZ2321</funding_grant_id><funding_grant_id>2024HBBHCXB031</funding_grant_id><funding_grant_id>GZC20240563, GZC20240554</funding_grant_id><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Yan J</pubmed_authors><pubmed_authors>Ouyang W</pubmed_authors><pubmed_authors>Ouyang X</pubmed_authors><pubmed_authors>Xing Y</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Wu C</pubmed_authors><pubmed_authors>Zheng R</pubmed_authors><pubmed_authors>Xie L</pubmed_authors><pubmed_authors>Shen C</pubmed_authors><pubmed_authors>Guan P</pubmed_authors><pubmed_authors>Foda M</pubmed_authors><pubmed_authors>Qiu L</pubmed_authors><pubmed_authors>Wu H</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Guo M</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Cao Z</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Huang X</pubmed_authors></additional><is_claimable>false</is_claimable><name>3D epigenome architecture orchestrates cis and trans regulation of flowering time in rice.</name><description>&lt;h4>Background&lt;/h4>Trimethylation of histone H3 lysine 27 (H3K27me3) confers a repressive chromatin state and is dynamically deposited and removed to regulate gene expression throughout plant growth and development. Nevertheless, the three-dimensional epigenome architecture linked to H3K27me3 and its regulatory role in controlling rice development remain unclear.&lt;h4>Results&lt;/h4>Here, we employ long-read ChIA-PET to map the genome topology associated with H3K27me3 in rice, identifying hundreds of repressive chromatin spatial clusters within chromosomes. The T-DNA insertional mutagenesis of EMBRYONIC FLOWER 2b (OsEMF2b) leads to disruption of H3K27me3-associated chromatin interaction networks. Notably, we discover that the three key flowering time loci, Early heading date 1 (Ehd1) and Headin</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-09T12:21:39.814Z</modification><creation>2026-07-09T11:17:34.682Z</creation></dates><accession>S-EPMC12930761</accession><cross_references><pubmed>41606643</pubmed><doi>10.1186/s13059-026-03940-3</doi></cross_references></HashMap>