Evidence map›Paper›PMID 42090559›Full record

ArticleGenome biology and evolution2026

Recurrent Modular Assembly Drives Independent Origins of Group II Introns Encoding LAGLIDADG Homing Endonucleases.

Feng Liu, Shuangle Jin, Qingbao Du

Abstract read
In one paragraph

Article in Genome biology and evolution, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Feng LiuLaboratory of Marine Ecology and Environmental Sciences, Institute of Oceanology, Chinese Academy of Sciences (IOCAS), Qingdao 266071, China.ORCID 0000-0002-5774-900X
Shuangle JinLaboratory of Marine Ecology and Environmental Sciences, Institute of Oceanology, Chinese Academy of Sciences (IOCAS), Qingdao 266071, China.ORCID 0009-0003-9693-0519
Qingbao DuTsingtao SINOVA-HK Biotechnology Co., Ltd., Qingdao 266400, China.ORCID 0000-0002-3561-4171

Funding

National Natural Science Foundation of China 42276133Shandong Provincial Key Research and Development Program Project 2025TSGCCZZB0313
6 · The paper itself

Abstract

Group II introns are catalytic RNAs that typically mobilize with intron-encoded reverse transcriptase/maturase (RT/M) proteins, yet a small subset encodes LAGLIDADG homing endonucleases (LHEs). The evolutionary mechanisms underlying this atypical RNA-protein association remain poorly understood. Here, we analyze 753 LHE-encoding group II introns (group II-LHE introns) from green algae, fungi, and bacteria to investigate their origins and structural diversification. Our comparative analyses reveal that these introns are distributed across four deeply divergent RNA backbone subclasses (IIA1, IIB1, IIB2, and IIC) and form 13 lineage-specific intron families. Secondary-structure reconstruction reveals a conserved catalytic core together with extensive family-specific remodeling, including variable LHE insertion sites, recurrent loss of branch-point adenosine, and differential retention of exon-recognition elements. Phylogenetic incongruence between the RNA backbone and LHE phylogenies supports multiple independent acquisitions rather than descent from a single ancestral composite element. These results demonstrate that LHE modules have been repeatedly recruited onto distinct group II intron scaffolds, highlighting recurrent modular assembly as a key mechanism in the evolution of RNA-protein mobile elements. Our study provides a unified framework for understanding the origin, diversification, and modular evolution of LHE-encoding group II introns.

Indexed as

EndonucleasesEvolution, MolecularIntronsBacteriaChlorophytaFungiNucleic Acid ConformationPhylogenyRNA, CatalyticEndonucleasesRNA, CatalyticLAGLIDADG homing endonucleasesmitochondrial intronsmobile genetic elementsmodular evolutionRNA–protein evolution

Identifiers

PMID42090559
PMCPMC13190283

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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.