Alignment of Genetic and Physical Maps of Gibberella zeae
We previously published a genetic map of Gibberella zeae (Fusarium graminearum sensu lato) based on a cross between Kansas strain Z-3639 (lineage 7) and Japanese strain R-5470 (lineage 6). In this study, that genetic map was aligned with the third assembly of the genomic sequence of G. zeae strain P...
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description | We previously published a genetic map of Gibberella zeae (Fusarium graminearum sensu lato) based on a cross between Kansas strain Z-3639 (lineage 7) and Japanese strain R-5470 (lineage 6). In this study, that genetic map was aligned with the third assembly of the genomic sequence of G. zeae strain PH-1 (lineage 7) using seven structural genes and 108 sequenced amplified fragment length polymorphism markers. Several linkage groups were combined based on the alignments, the nine original linkage groups were reduced to six groups, and the total size of the genetic map was reduced from 1,286 to 1,140 centimorgans. Nine supercontigs, comprising 99.2% of the genomic sequence assembly, were anchored to the genetic map. Eight markers (four markers from each parent) were not found in the genome assembly, and four of these markers were closely linked, suggesting that >150 kb of DNA sequence is missing from the PH-1 genome assembly. The alignments of the linkage groups and supercontigs yielded four independent sets, which is consistent with the four chromosomes reported for this fungus. Two proposed heterozygous inversions were confirmed by the alignments; otherwise, the colinearity of the genetic and physical maps was high. Two of four regions with segregation distortion were explained by the two selectable markers employed in making the cross. The average recombination rates for each chromosome were similar to those previously reported for G. zeae. Despite an inferred history of genetic isolation of lineage 6 and lineage 7, the chromosomes of these lineages remain homologous and are capable of recombination along their entire lengths, even within the inversions. This genetic map can now be used in conjunction with the physical sequence to study phenotypes (e.g., fertility and fitness) and genetic features (e.g., centromeres and recombination frequency) that do not have a known molecular signature in the genome. |
doi_str_mv | 10.1128/AEM.01866-07 |
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In this study, that genetic map was aligned with the third assembly of the genomic sequence of G. zeae strain PH-1 (lineage 7) using seven structural genes and 108 sequenced amplified fragment length polymorphism markers. Several linkage groups were combined based on the alignments, the nine original linkage groups were reduced to six groups, and the total size of the genetic map was reduced from 1,286 to 1,140 centimorgans. Nine supercontigs, comprising 99.2% of the genomic sequence assembly, were anchored to the genetic map. Eight markers (four markers from each parent) were not found in the genome assembly, and four of these markers were closely linked, suggesting that >150 kb of DNA sequence is missing from the PH-1 genome assembly. The alignments of the linkage groups and supercontigs yielded four independent sets, which is consistent with the four chromosomes reported for this fungus. Two proposed heterozygous inversions were confirmed by the alignments; otherwise, the colinearity of the genetic and physical maps was high. Two of four regions with segregation distortion were explained by the two selectable markers employed in making the cross. The average recombination rates for each chromosome were similar to those previously reported for G. zeae. Despite an inferred history of genetic isolation of lineage 6 and lineage 7, the chromosomes of these lineages remain homologous and are capable of recombination along their entire lengths, even within the inversions. This genetic map can now be used in conjunction with the physical sequence to study phenotypes (e.g., fertility and fitness) and genetic features (e.g., centromeres and recombination frequency) that do not have a known molecular signature in the genome.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AEM.01866-07</identifier><identifier>PMID: 18263740</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Amplified fragment length polymorphism ; Bacteria ; Base Sequence ; Biological and medical sciences ; blight ; Chromosome Mapping ; Chromosomes ; Chromosomes, Fungal - genetics ; DNA, Fungal - genetics ; Fundamental and applied biological sciences. Psychology ; Fungi ; Fusarium graminearum ; Genetic Linkage ; genetic markers ; genome ; Genome, Fungal ; Genomics ; Gibberella - genetics ; Gibberella zeae ; homologous recombination ; linkage (genetics) ; Microbiology ; Mycology ; Physical Chromosome Mapping ; plant pathogenic fungi ; Recombination, Genetic ; strains ; Studies</subject><ispartof>Applied and Environmental Microbiology, 2008-04, Vol.74 (8), p.2349-2359</ispartof><rights>2008 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Apr 2008</rights><rights>Copyright © 2008, American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c520t-bcc6204ef275b184225e4efb131c86a23a27d2c5aeeeaaf6ff81e74f22fb69753</citedby><cites>FETCH-LOGICAL-c520t-bcc6204ef275b184225e4efb131c86a23a27d2c5aeeeaaf6ff81e74f22fb69753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2293157/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2293157/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3186,3187,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20280757$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18263740$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Jungkwan</creatorcontrib><creatorcontrib>Jurgenson, James E</creatorcontrib><creatorcontrib>Leslie, John F</creatorcontrib><creatorcontrib>Bowden, Robert L</creatorcontrib><title>Alignment of Genetic and Physical Maps of Gibberella zeae</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>We previously published a genetic map of Gibberella zeae (Fusarium graminearum sensu lato) based on a cross between Kansas strain Z-3639 (lineage 7) and Japanese strain R-5470 (lineage 6). In this study, that genetic map was aligned with the third assembly of the genomic sequence of G. zeae strain PH-1 (lineage 7) using seven structural genes and 108 sequenced amplified fragment length polymorphism markers. Several linkage groups were combined based on the alignments, the nine original linkage groups were reduced to six groups, and the total size of the genetic map was reduced from 1,286 to 1,140 centimorgans. Nine supercontigs, comprising 99.2% of the genomic sequence assembly, were anchored to the genetic map. Eight markers (four markers from each parent) were not found in the genome assembly, and four of these markers were closely linked, suggesting that >150 kb of DNA sequence is missing from the PH-1 genome assembly. The alignments of the linkage groups and supercontigs yielded four independent sets, which is consistent with the four chromosomes reported for this fungus. Two proposed heterozygous inversions were confirmed by the alignments; otherwise, the colinearity of the genetic and physical maps was high. Two of four regions with segregation distortion were explained by the two selectable markers employed in making the cross. The average recombination rates for each chromosome were similar to those previously reported for G. zeae. Despite an inferred history of genetic isolation of lineage 6 and lineage 7, the chromosomes of these lineages remain homologous and are capable of recombination along their entire lengths, even within the inversions. This genetic map can now be used in conjunction with the physical sequence to study phenotypes (e.g., fertility and fitness) and genetic features (e.g., centromeres and recombination frequency) that do not have a known molecular signature in the genome.</description><subject>Amplified fragment length polymorphism</subject><subject>Bacteria</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>blight</subject><subject>Chromosome Mapping</subject><subject>Chromosomes</subject><subject>Chromosomes, Fungal - genetics</subject><subject>DNA, Fungal - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungi</subject><subject>Fusarium graminearum</subject><subject>Genetic Linkage</subject><subject>genetic markers</subject><subject>genome</subject><subject>Genome, Fungal</subject><subject>Genomics</subject><subject>Gibberella - genetics</subject><subject>Gibberella zeae</subject><subject>homologous recombination</subject><subject>linkage (genetics)</subject><subject>Microbiology</subject><subject>Mycology</subject><subject>Physical Chromosome Mapping</subject><subject>plant pathogenic fungi</subject><subject>Recombination, Genetic</subject><subject>strains</subject><subject>Studies</subject><issn>0099-2240</issn><issn>1098-5336</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtvFDEQhC0EIiFw4wwDEpyY0G57xvYFaRWFgJQIJMjZ6vHau47msdi7oPDr8T4UHhdOrVZ_KlV1MfaUwynnqN_Ozq9Ogeu2rUHdY8ccjK4bIdr77BjAmBpRwhF7lPMNAEho9UN2xDW2Qkk4ZmbWx8U4-HFdTaG68KNfR1fROK8-L29zdNRXV7TKu2PsOp9831P105N_zB4E6rN_cpgn7Pr9-dezD_Xlp4uPZ7PL2jUI67pzrkWQPqBqOq4lYuPL1nHBnW4JBaGao2vIe08U2hA090oGxNC1RjXihL3b66423eDnrlhN1NtVigOlWztRtH9fxri0i-m7RTSCN6oIvD4IpOnbxue1HWJ22xyjnzbZKpDaNFL-F0QuDTZia-nlP-DNtElj-YJFaIzSXPMCvdlDLk05Jx_uLHOw2-Zsac7umrOwdfnsz5i_4UNVBXh1ACiXWkKi0cV8xyGgBrWL-2LPLeNi-SMmbykPlvxglbTaopCmMM_3TKDJ0iIVnesvCFwAaC0USvELCO6zwg</recordid><startdate>20080401</startdate><enddate>20080401</enddate><creator>Lee, Jungkwan</creator><creator>Jurgenson, James E</creator><creator>Leslie, John F</creator><creator>Bowden, Robert L</creator><general>American Society for Microbiology</general><general>American Society for Microbiology (ASM)</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20080401</creationdate><title>Alignment of Genetic and Physical Maps of Gibberella zeae</title><author>Lee, Jungkwan ; Jurgenson, James E ; Leslie, John F ; Bowden, Robert L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-bcc6204ef275b184225e4efb131c86a23a27d2c5aeeeaaf6ff81e74f22fb69753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Amplified fragment length polymorphism</topic><topic>Bacteria</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>blight</topic><topic>Chromosome Mapping</topic><topic>Chromosomes</topic><topic>Chromosomes, Fungal - genetics</topic><topic>DNA, Fungal - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungi</topic><topic>Fusarium graminearum</topic><topic>Genetic Linkage</topic><topic>genetic markers</topic><topic>genome</topic><topic>Genome, Fungal</topic><topic>Genomics</topic><topic>Gibberella - genetics</topic><topic>Gibberella zeae</topic><topic>homologous recombination</topic><topic>linkage (genetics)</topic><topic>Microbiology</topic><topic>Mycology</topic><topic>Physical Chromosome Mapping</topic><topic>plant pathogenic fungi</topic><topic>Recombination, Genetic</topic><topic>strains</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Jungkwan</creatorcontrib><creatorcontrib>Jurgenson, James E</creatorcontrib><creatorcontrib>Leslie, John F</creatorcontrib><creatorcontrib>Bowden, Robert L</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Jungkwan</au><au>Jurgenson, James E</au><au>Leslie, John F</au><au>Bowden, Robert L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alignment of Genetic and Physical Maps of Gibberella zeae</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2008-04-01</date><risdate>2008</risdate><volume>74</volume><issue>8</issue><spage>2349</spage><epage>2359</epage><pages>2349-2359</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><eissn>1098-6596</eissn><coden>AEMIDF</coden><abstract>We previously published a genetic map of Gibberella zeae (Fusarium graminearum sensu lato) based on a cross between Kansas strain Z-3639 (lineage 7) and Japanese strain R-5470 (lineage 6). In this study, that genetic map was aligned with the third assembly of the genomic sequence of G. zeae strain PH-1 (lineage 7) using seven structural genes and 108 sequenced amplified fragment length polymorphism markers. Several linkage groups were combined based on the alignments, the nine original linkage groups were reduced to six groups, and the total size of the genetic map was reduced from 1,286 to 1,140 centimorgans. Nine supercontigs, comprising 99.2% of the genomic sequence assembly, were anchored to the genetic map. Eight markers (four markers from each parent) were not found in the genome assembly, and four of these markers were closely linked, suggesting that >150 kb of DNA sequence is missing from the PH-1 genome assembly. The alignments of the linkage groups and supercontigs yielded four independent sets, which is consistent with the four chromosomes reported for this fungus. Two proposed heterozygous inversions were confirmed by the alignments; otherwise, the colinearity of the genetic and physical maps was high. Two of four regions with segregation distortion were explained by the two selectable markers employed in making the cross. The average recombination rates for each chromosome were similar to those previously reported for G. zeae. Despite an inferred history of genetic isolation of lineage 6 and lineage 7, the chromosomes of these lineages remain homologous and are capable of recombination along their entire lengths, even within the inversions. This genetic map can now be used in conjunction with the physical sequence to study phenotypes (e.g., fertility and fitness) and genetic features (e.g., centromeres and recombination frequency) that do not have a known molecular signature in the genome.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>18263740</pmid><doi>10.1128/AEM.01866-07</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amplified fragment length polymorphism Bacteria Base Sequence Biological and medical sciences blight Chromosome Mapping Chromosomes Chromosomes, Fungal - genetics DNA, Fungal - genetics Fundamental and applied biological sciences. Psychology Fungi Fusarium graminearum Genetic Linkage genetic markers genome Genome, Fungal Genomics Gibberella - genetics Gibberella zeae homologous recombination linkage (genetics) Microbiology Mycology Physical Chromosome Mapping plant pathogenic fungi Recombination, Genetic strains Studies |
title | Alignment of Genetic and Physical Maps of Gibberella zeae |
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