Evidence map›Paper›PMID 41491960›Full record

ArticleBiology direct2026

Integrative multi-omics analysis widens annotation and functional insights into long non-coding RNAs of Arabidopsis thaliana.

A T Vivek, Harikumar Kiran, Namrata Sahu, Garima Kalakoti, Shailesh Kumar

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Article in Biology direct, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

A T VivekBioinformatics Lab, BRIC-National Institute of Plant Genome research(NIPGR), Aruna Asaf Ali Marg, New Delhi, 110067, India.ORCID http://orcid.org/0000-0003-2046-4841
Harikumar KiranBioinformatics Lab, BRIC-National Institute of Plant Genome research(NIPGR), Aruna Asaf Ali Marg, New Delhi, 110067, India.
Namrata SahuBioinformatics Lab, BRIC-National Institute of Plant Genome research(NIPGR), Aruna Asaf Ali Marg, New Delhi, 110067, India.
Garima KalakotiBioinformatics Lab, BRIC-National Institute of Plant Genome research(NIPGR), Aruna Asaf Ali Marg, New Delhi, 110067, India.ORCID http://orcid.org/0009-0005-2880-2800
Shailesh KumarBioinformatics Lab, BRIC-National Institute of Plant Genome research(NIPGR), Aruna Asaf Ali Marg, New Delhi, 110067, India. shailesh@nipgr.ac.in.ORCID https://orcid.org/0000-0002-1872-9903

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLong non-coding RNAs (lncRNAs) play key roles in regulating plant growth, development, and stress responses. Despite their increasing identification in plant transcriptomes, a systematic characterization of lncRNAs is still lacking, leaving a significant knowledge gap. To address this, we systematically identified and characterized Arabidopsis lncRNAs through integrative analysis of strand-specific RNA sequencing data and multi-omics datasets, revealing their genomic features, regulatory interactions, and evolutionary characteristics.

resultsUsing a custom pipeline applied to hundreds of stranded RNA-seq datasets, we assembled a comprehensive catalog of 4,772 intergenic and antisense Arabidopsis lncRNAs. In comparing multiple key features of lncRNAs with those of protein-coding genes, we found that intergenic lncRNAs contain high transposable element-derived fragments and display broader TE diversity. Distinct DNA methylation and histone modification signatures further distinguished lncRNAs from protein-coding genes. We additionally uncovered R-loop connections and associations with sRNAs involved in post-transcriptional regulation and RNA-directed DNA methylation, with a minor subset classified as Pol V–transcribed. Of note, our results revealed lncRNAs mediating stress-responsive cis interactions and others linked to trait-associated loci. Probing further, an experimental evidence resource confirmed small peptide production from multiple lncRNA loci. Extending our investigation, comparative analyses across Brassicaceae species revealed syntenic lncRNAs enriched for shared sequence motifs despite substantial sequence divergence.

conclusionsThis study provides a valuable and extensively annotated catalog of Arabidopsis lncRNAs, revealing their diverse genomic features, regulatory interactions, and evolutionary characteristics. Altogether, our work advocates for multi-omics integrative analysis as a potent strategy to efficiently enhance lncRNA annotation, providing insights into functionality and addressing annotation limitations. Our comprehensive bioinformatic analyses of Arabidopsis lncRNAs pave the way for future functional characterization of these transcripts.

Indexed as

ArabidopsisRNA, Long NoncodingRNA, PlantGene Expression Regulation, PlantGenome, PlantMolecular Sequence AnnotationMultiomicsTranscriptomeRNA, Long NoncodingRNA, PlantArabidopsis thalianaBioinformaticsepigeneticsEvolutionlncRNA-sRNA interactionLong non-coding RNAsMulti-omicsRdDM pathwayStrand-specific RNA-seq

Identifiers

PMID41491960
PMCPMC12870029

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.