Evidence map›Paper›PMID 41420151›Full record

ArticleBMC genomics2025

Evolutionary dynamics of the proanthocyanidin biosynthesis gene LAR.

Maria F Marin-Recinos, Boas Pucker

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Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Maria F Marin-RecinosPlant Biotechnology and Bioinformatics, Institute for Cellular and Molecular Botany - IZMB, University of Bonn, Kirschalle 1, 53115, Bonn, Germany.
Boas PuckerPlant Biotechnology and Bioinformatics, Institute for Cellular and Molecular Botany - IZMB, University of Bonn, Kirschalle 1, 53115, Bonn, Germany. pucker@uni-bonn.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeucoanthocyanidin reductase (LAR) is a key enzyme in proanthocyanidin (PAs) biosynthesis, catalyzing the conversion of leucoanthocyanidins to catechins. While early steps in the flavonoid pathway are broadly conserved across plant lineages, increasing evidence demonstrates lineage-specific evolutionary trajectories and functional diversification in its terminal branches, particularly in the case of LAR. To explore the evolutionary dynamics and functional divergence of LAR genes, we conducted large-scale comparative and phylogenetic analyses across major plant clades.

resultsThe phylogenetic analysis revealed multiple independent duplication events and lineage-specific expansions of LAR lineages, particularly among dicots and gymnosperms. In dicots, LAR1 and LAR2 were differentially retained and diversified, whereas gymnosperm LAR homologs formed early-diverging clades, suggesting an ancient duplication and potential neofunctionalization. Coexpression analyses across species and tissues indicate paralog-specific expression patterns. Sequence analysis identified both conserved and clade-specific protein domains, supporting functional divergence. Promoter analyses showed differences in transcription factor binding site composition between LAR1 and LAR2, pointing to regulatory sub- or neo-functionalization. Lastly, synteny analyses support the potential absence of LAR in multiple Brassicales genomes.

conclusionsLAR shows evidence of evolutionary diversification, shaped by both coding and regulatory changes. These patterns of diversification help explain variation in flavonoid profiles in gymnosperms and angiosperms. Understanding the evolutionary dynamics of LAR not only deepens our knowledge of metabolic pathway evolution but also provides insights relevant to the breeding and metabolic engineering of plant traits related to pigmentation, stress resilience, and nutritional quality.

Indexed as

Evolution, MolecularPlant ProteinsProanthocyanidinsGene DuplicationGene Expression Regulation, PlantGenes, PlantPhylogenyPromoter Regions, GeneticPlant ProteinsproanthocyanidinProanthocyanidinsEvolutionFlavonoid biosynthesisGene duplicationLAR1LAR2Leucoanthocyanidin reductaseProanthocyanidinSubfunctionalization

Identifiers

PMID41420151
PMCPMC12831355

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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.