<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li X</submitter><funding>United Soybean Board</funding><funding>National Science Foundation</funding><pagination>koaf279</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12679596</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>37(12)</volume><pubmed_abstract>Gene duplication is a major source of evolutionary innovation, enabling the emergence of novel expression patterns and functions. Leveraging single-cell genomics, we investigated the transcriptional and cis-regulatory landscapes of duplicated genes in cultivated soybean (Glycine max), which has undergone 2 rounds of whole-genome duplication. Our analysis revealed extensive diversity of transcriptional profiles within and across tissues among duplicated gene pairs. Within-tissue divergence was largely attributable to genetic variation in their associated accessible chromatin regions (ACRs), where cis-regulatory elements reside, whereas cross-tissue divergence was more likely shaped by dynamics in ACR chromatin accessibility profiles across tissues. Distinct duplication mechanisms also likely give rise to different types of cis-regulatory variants, contributing variably to transcriptional divergence. By comparing ACRs associated with gene sets derived from 2 rounds of whole-genome duplication and sharing a common ancestral gene, we found that most ACRs retained one or multiple corresponding duplicated sequences in which mutations gradually accumulated over time, while a subset likely arose de novo. Finally, we traced the evolution of cell-type-specific expression and cell-type-specific ACRs within duplicated gene sets, illustrating a powerful framework for identifying candidate regulatory regions driving cell-type-specific expression. Collectively, our findings highlight the important role of cis-regulatory evolution in shaping transcriptional divergence in a spatiotemporal manner, uncovered with the resolution of single-cell genomics.</pubmed_abstract><journal>The Plant cell</journal><pubmed_title>From duplication to divergence: Single-cell insights into transcriptional and cis-regulatory landscapes in soybean.</pubmed_title><pmcid>PMC12679596</pmcid><funding_grant_id>IOS-1856627</funding_grant_id><funding_grant_id>2432-201-0102</funding_grant_id><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Schmitz RJ</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors></additional><is_claimable>false</is_claimable><name>From duplication to divergence: Single-cell insights into transcriptional and cis-regulatory landscapes in soybean.</name><description>Gene duplication is a major source of evolutionary innovation, enabling the emergence of novel expression patterns and functions. Leveraging single-cell genomics, we investigated the transcriptional and cis-regulatory landscapes of duplicated genes in cultivated soybean (Glycine max), which has undergone 2 rounds of whole-genome duplication. Our analysis revealed extensive diversity of transcriptional profiles within and across tissues among duplicated gene pairs. Within-tissue divergence was largely attributable to genetic variation in their associated accessible chromatin regions (ACRs), where cis-regulatory elements reside, whereas cross-tissue divergence was more likely shaped by dynamics in ACR chromatin accessibility profiles across tissues. Distinct duplication mechanisms also likely give rise to different types of cis-regulatory variants, contributing variably to transcriptional divergence. By comparing ACRs associated with gene sets derived from 2 rounds of whole-genome duplication and sharing a common ancestral gene, we found that most ACRs retained one or multiple corresponding duplicated sequences in which mutations gradually accumulated over time, while a subset likely arose de novo. Finally, we traced the evolution of cell-type-specific expression and cell-type-specific ACRs within duplicated gene sets, illustrating a powerful framework for identifying candidate regulatory regions driving cell-type-specific expression. Collectively, our findings highlight the important role of cis-regulatory evolution in shaping transcriptional divergence in a spatiotemporal manner, uncovered with the resolution of single-cell genomics.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-05-23T03:16:36.605Z</modification><creation>2026-05-23T03:10:11.869Z</creation></dates><accession>S-EPMC12679596</accession><cross_references><pubmed>41285681</pubmed><doi>10.1093/plcell/koaf279</doi></cross_references></HashMap>