The genome sequence of the popular hexose-transport-deficient Saccharomyces cerevisiae strain EBY.VW4000 reveals LoxP/Cre-induced translocations and gene loss
Saccharomyces cerevisiae harbours a large group of tightly controlled hexose transporters with different characteristics. Construction and characterization of S. cerevisiae EBY.VW4000, a strain devoid of glucose import, was a milestone in hexose-transporter research. This strain has become a widely...
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description | Saccharomyces cerevisiae harbours a large group of tightly controlled hexose transporters with different characteristics. Construction and characterization of S. cerevisiae EBY.VW4000, a strain devoid of glucose import, was a milestone in hexose-transporter research. This strain has become a widely used platform for discovery and characterization of transporters from a wide range of organisms. To abolish glucose uptake, 21 genes were knocked out, involving 16 successive deletion rounds with the LoxP/Cre system. Although such intensive modifications are known to increase the risk of genome alterations, the genome of EBY.VW4000 has hitherto not been characterized. Based on a combination of whole genome sequencing, karyotyping and molecular confirmation, the present study reveals that construction of EBY.VW4000 resulted in gene losses and chromosomal rearrangements. Recombinations between the LoxP scars have led to the assembly of four neo-chromosomes, truncation of two chromosomes and loss of two subtelomeric regions. Furthermore, sporulation and spore germination are severely impaired in EBY.VW4000. Karyotyping of the EBY.VW4000 lineage retraced its current chromosomal architecture to four translocations events occurred between the 6th and the 12th rounds of deletion. The presented data facilitate further studies on EBY.VW4000 and highlight the risks of genome alterations associated with repeated use of the LoxP/Cre system.
Characterization of the popular Saccharomyces cerevisiae strain EBY.VW4000, devoid of glucose uptake, revealed that intensive genetic manipulations have caused LoxP/Cre-induced gene losses and chromosomal translocations, and phenotypic alterations. |
doi_str_mv | 10.1093/femsyr/fou004 |
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Characterization of the popular Saccharomyces cerevisiae strain EBY.VW4000, devoid of glucose uptake, revealed that intensive genetic manipulations have caused LoxP/Cre-induced gene losses and chromosomal translocations, and phenotypic alterations.</description><identifier>ISSN: 1567-1356</identifier><identifier>EISSN: 1567-1364</identifier><identifier>DOI: 10.1093/femsyr/fou004</identifier><identifier>PMID: 25673752</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Biological Transport ; Chromosome rearrangements ; Chromosome translocations ; Chromosomes ; DNA, Fungal - chemistry ; DNA, Fungal - genetics ; Gene Deletion ; Gene Rearrangement ; Genome, Fungal ; Genomes ; Hexose ; Hexoses - metabolism ; Karyotyping ; Metabolic Engineering ; Nucleotide sequence ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - metabolism ; Sequence Analysis, DNA ; Spore germination ; Sporulation ; Translocation, Genetic ; Whole genome sequencing ; Yeast</subject><ispartof>FEMS yeast research, 2015-03, Vol.15 (2)</ispartof><rights>FEMS 2015. All rights reserved. For permissions, please e-mail: journals.permission@oup.com 2015</rights><rights>FEMS 2015. All rights reserved. For permissions, please e-mail: journals.permission@oup.com.</rights><rights>FEMS 2015. All rights reserved. For permissions, please e-mail: journals.permission@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-bbbe2b1c74d488bf205a9d772414d82a1d74764dbf3e04cc7aa0aa1b87b364873</citedby><cites>FETCH-LOGICAL-c393t-bbbe2b1c74d488bf205a9d772414d82a1d74764dbf3e04cc7aa0aa1b87b364873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1598,27901,27902</link.rule.ids><linktorsrc>$$Uhttps://dx.doi.org/10.1093/femsyr/fou004$$EView_record_in_Oxford_University_Press$$FView_record_in_$$GOxford_University_Press</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25673752$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Solis-Escalante, Daniel</creatorcontrib><creatorcontrib>van den Broek, Marcel</creatorcontrib><creatorcontrib>Kuijpers, Niels G. A.</creatorcontrib><creatorcontrib>Pronk, Jack T.</creatorcontrib><creatorcontrib>Boles, Eckhard</creatorcontrib><creatorcontrib>Daran, Jean-Marc</creatorcontrib><creatorcontrib>Daran-Lapujade, Pascale</creatorcontrib><title>The genome sequence of the popular hexose-transport-deficient Saccharomyces cerevisiae strain EBY.VW4000 reveals LoxP/Cre-induced translocations and gene loss</title><title>FEMS yeast research</title><addtitle>FEMS Yeast Res</addtitle><description>Saccharomyces cerevisiae harbours a large group of tightly controlled hexose transporters with different characteristics. Construction and characterization of S. cerevisiae EBY.VW4000, a strain devoid of glucose import, was a milestone in hexose-transporter research. This strain has become a widely used platform for discovery and characterization of transporters from a wide range of organisms. To abolish glucose uptake, 21 genes were knocked out, involving 16 successive deletion rounds with the LoxP/Cre system. Although such intensive modifications are known to increase the risk of genome alterations, the genome of EBY.VW4000 has hitherto not been characterized. Based on a combination of whole genome sequencing, karyotyping and molecular confirmation, the present study reveals that construction of EBY.VW4000 resulted in gene losses and chromosomal rearrangements. Recombinations between the LoxP scars have led to the assembly of four neo-chromosomes, truncation of two chromosomes and loss of two subtelomeric regions. Furthermore, sporulation and spore germination are severely impaired in EBY.VW4000. Karyotyping of the EBY.VW4000 lineage retraced its current chromosomal architecture to four translocations events occurred between the 6th and the 12th rounds of deletion. The presented data facilitate further studies on EBY.VW4000 and highlight the risks of genome alterations associated with repeated use of the LoxP/Cre system.
Characterization of the popular Saccharomyces cerevisiae strain EBY.VW4000, devoid of glucose uptake, revealed that intensive genetic manipulations have caused LoxP/Cre-induced gene losses and chromosomal translocations, and phenotypic alterations.</description><subject>Biological Transport</subject><subject>Chromosome rearrangements</subject><subject>Chromosome translocations</subject><subject>Chromosomes</subject><subject>DNA, Fungal - chemistry</subject><subject>DNA, Fungal - genetics</subject><subject>Gene Deletion</subject><subject>Gene Rearrangement</subject><subject>Genome, Fungal</subject><subject>Genomes</subject><subject>Hexose</subject><subject>Hexoses - metabolism</subject><subject>Karyotyping</subject><subject>Metabolic Engineering</subject><subject>Nucleotide sequence</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Sequence Analysis, DNA</subject><subject>Spore germination</subject><subject>Sporulation</subject><subject>Translocation, Genetic</subject><subject>Whole genome sequencing</subject><subject>Yeast</subject><issn>1567-1356</issn><issn>1567-1364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkUtP3DAUha0KVB7tsltkiQ2bMH4lzixhBLTSSCBBW3UV-XHTMUrs1E4Q82f4rXg6lEpsWNny_Xx07jkIfaHklJI5n7XQp3WctWEiRHxA-7SsZEF5JXZe72W1hw5SuieESkLqj2iP5QGXJdtHT3crwL_Bhx5wgj8TeAM4tHjMz0MYpk5FvILHkKAYo_JpCHEsLLTOOPAjvlXGrFQM_dpAwgYiPLjkVNbKtPP44vzX6Y-fghCC8whUl_AyPN7MFhEK5-1kwOK_ul0wanTBJ6y83RgC3IWUPqHdNn-Czy_nIfp-eXG3-Fosr6--Lc6WheFzPhZaa2CaGimsqGvdMlKquZWSCSpszRS1UshKWN1yIMIYqRRRiupa6pxULfkhOtnqDjHkENLY9C4Z6DrlIUypoVVZ5tBYOc_o8Rv0PkzRZ3cN41ywitRiQxVbysS8RoS2GaLrVVw3lDSb4pptcc22uMwfvahOugf7Sv9r6r_DMA3vaD0Dq-mmaw</recordid><startdate>20150301</startdate><enddate>20150301</enddate><creator>Solis-Escalante, Daniel</creator><creator>van den Broek, Marcel</creator><creator>Kuijpers, Niels G. 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A.</creatorcontrib><creatorcontrib>Pronk, Jack T.</creatorcontrib><creatorcontrib>Boles, Eckhard</creatorcontrib><creatorcontrib>Daran, Jean-Marc</creatorcontrib><creatorcontrib>Daran-Lapujade, Pascale</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS yeast research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Solis-Escalante, Daniel</au><au>van den Broek, Marcel</au><au>Kuijpers, Niels G. A.</au><au>Pronk, Jack T.</au><au>Boles, Eckhard</au><au>Daran, Jean-Marc</au><au>Daran-Lapujade, Pascale</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The genome sequence of the popular hexose-transport-deficient Saccharomyces cerevisiae strain EBY.VW4000 reveals LoxP/Cre-induced translocations and gene loss</atitle><jtitle>FEMS yeast research</jtitle><addtitle>FEMS Yeast Res</addtitle><date>2015-03-01</date><risdate>2015</risdate><volume>15</volume><issue>2</issue><issn>1567-1356</issn><eissn>1567-1364</eissn><abstract>Saccharomyces cerevisiae harbours a large group of tightly controlled hexose transporters with different characteristics. Construction and characterization of S. cerevisiae EBY.VW4000, a strain devoid of glucose import, was a milestone in hexose-transporter research. This strain has become a widely used platform for discovery and characterization of transporters from a wide range of organisms. To abolish glucose uptake, 21 genes were knocked out, involving 16 successive deletion rounds with the LoxP/Cre system. Although such intensive modifications are known to increase the risk of genome alterations, the genome of EBY.VW4000 has hitherto not been characterized. Based on a combination of whole genome sequencing, karyotyping and molecular confirmation, the present study reveals that construction of EBY.VW4000 resulted in gene losses and chromosomal rearrangements. Recombinations between the LoxP scars have led to the assembly of four neo-chromosomes, truncation of two chromosomes and loss of two subtelomeric regions. Furthermore, sporulation and spore germination are severely impaired in EBY.VW4000. Karyotyping of the EBY.VW4000 lineage retraced its current chromosomal architecture to four translocations events occurred between the 6th and the 12th rounds of deletion. The presented data facilitate further studies on EBY.VW4000 and highlight the risks of genome alterations associated with repeated use of the LoxP/Cre system.
Characterization of the popular Saccharomyces cerevisiae strain EBY.VW4000, devoid of glucose uptake, revealed that intensive genetic manipulations have caused LoxP/Cre-induced gene losses and chromosomal translocations, and phenotypic alterations.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>25673752</pmid><doi>10.1093/femsyr/fou004</doi><oa>free_for_read</oa></addata></record> |
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subjects | Biological Transport Chromosome rearrangements Chromosome translocations Chromosomes DNA, Fungal - chemistry DNA, Fungal - genetics Gene Deletion Gene Rearrangement Genome, Fungal Genomes Hexose Hexoses - metabolism Karyotyping Metabolic Engineering Nucleotide sequence Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae - metabolism Sequence Analysis, DNA Spore germination Sporulation Translocation, Genetic Whole genome sequencing Yeast |
title | The genome sequence of the popular hexose-transport-deficient Saccharomyces cerevisiae strain EBY.VW4000 reveals LoxP/Cre-induced translocations and gene loss |
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