Evidence map›Paper›PMID 16297239›Full record

ArticleBMC genomics2005

An acquisition account of genomic islands based on genome signature comparisons.

M W J van Passel, A Bart, H H Thygesen, A C M Luyf, A H C van Kampen, A van der Ende

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In one paragraph

Article in BMC genomics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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  17. Viral metagenomics.Reviews in medical virology
    Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

M W J van PasselDepartment of Medical Microbiology, Academic Medical Center, Amsterdam, The Netherlands. m.w.vanpassel@amc.uva.nl
A Bart
H H Thygesen
A C M Luyf
A H C van Kampen
A van der Ende

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent analyses of prokaryotic genome sequences have demonstrated the important force horizontal gene transfer constitutes in genome evolution. Horizontally acquired sequences are detectable by, among others, their dinucleotide composition (genome signature) dissimilarity with the host genome. Genomic islands (GIs) comprise important and interesting horizontally transferred sequences, but information about acquisition events or relatedness between GIs is scarce. In Vibrio vulnificus CMCP6, 10 and 11 GIs have previously been identified in the sequenced chromosomes I and II, respectively. We assessed the compositional similarity and putative acquisition account of these GIs using the genome signature. For this analysis we developed a new algorithm, available as a web application.

resultsOf 21 GIs, VvI-1 and VvI-10 of chromosome I have similar genome signatures, and while artificially divided due to a linear annotation, they are adjacent on the circular chromosome and therefore comprise one GI. Similarly, GIs VvI-3 and VvI-4 of chromosome I together with the region between these two islands are compositionally similar, suggesting that they form one GI (making a total of 19 GIs in chromosome I + chromosome II). Cluster analysis assigned the 19 GIs to 11 different branches above our conservative threshold. This suggests a limited number of compositionally similar donors or intragenomic dispersion of ancestral acquisitions. Furthermore, 2 GIs of chromosome II cluster with chromosome I, while none of the 19 GIs group with chromosome II, suggesting an unidirectional dispersal of large anomalous gene clusters from chromosome I to chromosome II.

conclusionFrom the results, we infer 10 compositionally dissimilar donors for 19 GIs in the V. vulnificus CMCP6 genome, including chromosome I donating to chromosome II. This suggests multiple transfer events from individual donor types or from donors with similar genome signatures. Applied to other prokaryotes, this approach may elucidate the acquisition account in their genome sequences, and facilitate donor identification of GIs.

Indexed as

Gene Transfer TechniquesGenomeGenomic IslandsAlgorithmsBase SequenceChromosome MappingChromosomesChromosomes, BacterialCluster AnalysisEvolution, MolecularGene Expression ProfilingGenes, BacterialGenetic LinkageGene Transfer, HorizontalGenome, BacterialGenomics

Identifiers

PMID16297239
PMCPMC1310630

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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.