Evidence map›Paper›PMID 34018328›Full record

ArticleMolecular systems biology2021

Sequence analysis of tyrosine recombinases allows annotation of mobile genetic elements in prokaryotic genomes.

Georgy Smyshlyaev, Alex Bateman, Orsolya Barabas

Abstract read
In one paragraph

Article in Molecular systems biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

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0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

43 citing papers in PubMed.

  1. Article
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  4. Differentiating commensal and disease-associatedFrontiers in veterinary science · 2026
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  5. Description and evolution of aFrontiers in microbiology · 2026
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  18. Complete genomes ofMicrobial genomics · 2024
    Article
  19. Annotation and Comparative Genomics of Prokaryotic Transposable Elements.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Georgy SmyshlyaevEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.ORCID 0000-0003-4637-4027
Alex BatemanEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.ORCID 0000-0002-6982-4660
Orsolya BarabasEuropean Molecular Biology Laboratory (EMBL), Structural and Computational Biology Unit, Heidelberg, Germany.ORCID 0000-0002-2873-5872

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mobile genetic elements (MGEs) sequester and mobilize antibiotic resistance genes across bacterial genomes. Efficient and reliable identification of such elements is necessary to follow resistance spreading. However, automated tools for MGE identification are missing. Tyrosine recombinase (YR) proteins drive MGE mobilization and could provide markers for MGE detection, but they constitute a diverse family also involved in housekeeping functions. Here, we conducted a comprehensive survey of YRs from bacterial, archaeal, and phage genomes and developed a sequence-based classification system that dissects the characteristics of MGE-borne YRs. We revealed that MGE-related YRs evolved from non-mobile YRs by acquisition of a regulatory arm-binding domain that is essential for their mobility function. Based on these results, we further identified numerous unknown MGEs. This work provides a resource for comparative analysis and functional annotation of YRs and aids the development of computational tools for MGE annotation. Additionally, we reveal how YRs adapted to drive gene transfer across species and provide a tool to better characterize antibiotic resistance dissemination.

Indexed as

ArchaeaBacteriaDrug Resistance, MicrobialEvolution, MolecularFungiInterspersed Repetitive SequencesMolecular Sequence AnnotationRecombinasesSequence Analysis, ProteinSystems BiologyRecombinasesantibiotic resistanceevolutionhorizontal gene transfermobile genetic elementstyrosine recombinases

Identifiers

PMID34018328
PMCPMC8138268

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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.