An acquisition account of genomic islands based on genome signature comparisons
<p>Abstract</p> <p>Background</p> <p>Recent 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 compo...
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doaj-9d0f3d6792a94d7c854202888da5aa0b2020-11-25T00:25:00ZengBMCBMC Genomics1471-21642005-11-016116310.1186/1471-2164-6-163An acquisition account of genomic islands based on genome signature comparisonsLuyf ACMThygesen HHBart Avan Passel MWJvan Kampen AHCvan der Ende A<p>Abstract</p> <p>Background</p> <p>Recent 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 <it>Vibrio vulnificus </it>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.</p> <p>Results</p> <p>Of 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.</p> <p>Conclusion</p> <p>From the results, we infer 10 compositionally dissimilar donors for 19 GIs in the <it>V. vulnificus </it>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.</p> http://www.biomedcentral.com/1471-2164/6/163 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Luyf ACM Thygesen HH Bart A van Passel MWJ van Kampen AHC van der Ende A |
spellingShingle |
Luyf ACM Thygesen HH Bart A van Passel MWJ van Kampen AHC van der Ende A An acquisition account of genomic islands based on genome signature comparisons BMC Genomics |
author_facet |
Luyf ACM Thygesen HH Bart A van Passel MWJ van Kampen AHC van der Ende A |
author_sort |
Luyf ACM |
title |
An acquisition account of genomic islands based on genome signature comparisons |
title_short |
An acquisition account of genomic islands based on genome signature comparisons |
title_full |
An acquisition account of genomic islands based on genome signature comparisons |
title_fullStr |
An acquisition account of genomic islands based on genome signature comparisons |
title_full_unstemmed |
An acquisition account of genomic islands based on genome signature comparisons |
title_sort |
acquisition account of genomic islands based on genome signature comparisons |
publisher |
BMC |
series |
BMC Genomics |
issn |
1471-2164 |
publishDate |
2005-11-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Recent 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 <it>Vibrio vulnificus </it>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.</p> <p>Results</p> <p>Of 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.</p> <p>Conclusion</p> <p>From the results, we infer 10 compositionally dissimilar donors for 19 GIs in the <it>V. vulnificus </it>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.</p> |
url |
http://www.biomedcentral.com/1471-2164/6/163 |
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