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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Veröffentlicht in:Applied and Environmental Microbiology 2008-04, Vol.74 (8), p.2349-2359
Hauptverfasser: Lee, Jungkwan, Jurgenson, James E, Leslie, John F, Bowden, Robert L
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Jurgenson, James E
Leslie, John F
Bowden, Robert L
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.
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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 &gt;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. 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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&amp;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). 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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. 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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. 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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 &gt;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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source American Society for Microbiology; MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection
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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