Sequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse.

Gross chromosomal rearrangements have the potential to be evolutionarily advantageous to an adapting organism. The generation of a hybrid species increases opportunity for recombination by bringing together two homologous genomes. We sought to define the location of genomic rearrangements in three s...

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Autores principales: Sarah K Hewitt, Ian J Donaldson, Simon C Lovell, Daniela Delneri
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Publicado: Public Library of Science (PLoS) 2014
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spelling oai:doaj.org-article:097d6bfa6fca41b99c027ce3588d017b2021-11-18T08:27:32ZSequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse.1932-620310.1371/journal.pone.0092203https://doaj.org/article/097d6bfa6fca41b99c027ce3588d017b2014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24643015/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Gross chromosomal rearrangements have the potential to be evolutionarily advantageous to an adapting organism. The generation of a hybrid species increases opportunity for recombination by bringing together two homologous genomes. We sought to define the location of genomic rearrangements in three strains of Saccharomyces pastorianus, a natural lager-brewing yeast hybrid of Saccharomyces cerevisiae and Saccharomyces eubayanus, using whole genome shotgun sequencing. Each strain of S. pastorianus has lost species-specific portions of its genome and has undergone extensive recombination, producing chimeric chromosomes. We predicted 30 breakpoints that we confirmed at the single nucleotide level by designing species-specific primers that flank each breakpoint, and then sequencing the PCR product. These rearrangements are the result of recombination between areas of homology between the two subgenomes, rather than repetitive elements such as transposons or tRNAs. Interestingly, 28/30 S. cerevisiae-S. eubayanus recombination breakpoints are located within genic regions, generating chimeric genes. Furthermore we show evidence for the reuse of two breakpoints, located in HSP82 and KEM1, in strains of proposed independent origin.Sarah K HewittIan J DonaldsonSimon C LovellDaniela DelneriPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 3, p e92203 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Sarah K Hewitt
Ian J Donaldson
Simon C Lovell
Daniela Delneri
Sequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse.
description Gross chromosomal rearrangements have the potential to be evolutionarily advantageous to an adapting organism. The generation of a hybrid species increases opportunity for recombination by bringing together two homologous genomes. We sought to define the location of genomic rearrangements in three strains of Saccharomyces pastorianus, a natural lager-brewing yeast hybrid of Saccharomyces cerevisiae and Saccharomyces eubayanus, using whole genome shotgun sequencing. Each strain of S. pastorianus has lost species-specific portions of its genome and has undergone extensive recombination, producing chimeric chromosomes. We predicted 30 breakpoints that we confirmed at the single nucleotide level by designing species-specific primers that flank each breakpoint, and then sequencing the PCR product. These rearrangements are the result of recombination between areas of homology between the two subgenomes, rather than repetitive elements such as transposons or tRNAs. Interestingly, 28/30 S. cerevisiae-S. eubayanus recombination breakpoints are located within genic regions, generating chimeric genes. Furthermore we show evidence for the reuse of two breakpoints, located in HSP82 and KEM1, in strains of proposed independent origin.
format article
author Sarah K Hewitt
Ian J Donaldson
Simon C Lovell
Daniela Delneri
author_facet Sarah K Hewitt
Ian J Donaldson
Simon C Lovell
Daniela Delneri
author_sort Sarah K Hewitt
title Sequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse.
title_short Sequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse.
title_full Sequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse.
title_fullStr Sequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse.
title_full_unstemmed Sequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse.
title_sort sequencing and characterisation of rearrangements in three s. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/097d6bfa6fca41b99c027ce3588d017b
work_keys_str_mv AT sarahkhewitt sequencingandcharacterisationofrearrangementsinthreespastorianusstrainsrevealsthepresenceofchimericgenesandgivesevidenceofbreakpointreuse
AT ianjdonaldson sequencingandcharacterisationofrearrangementsinthreespastorianusstrainsrevealsthepresenceofchimericgenesandgivesevidenceofbreakpointreuse
AT simonclovell sequencingandcharacterisationofrearrangementsinthreespastorianusstrainsrevealsthepresenceofchimericgenesandgivesevidenceofbreakpointreuse
AT danieladelneri sequencingandcharacterisationofrearrangementsinthreespastorianusstrainsrevealsthepresenceofchimericgenesandgivesevidenceofbreakpointreuse
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