Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12
Identifieur interne : 000C88 ( Istex/Corpus ); précédent : 000C87; suivant : 000C89Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12
Auteurs : H. S. Sun ; L. Cai ; S. K. Davis ; J. F. Taylor ; L. K. Doud ; M. D. Bishop ; H. Hayes ; W. Barendse ; D. Vaiman ; R. A. Mcgraw ; T. Hirano ; Y. Sugimoto ; B. W. KirkpatrickSource :
- Genomics [ 0888-7543 ] ; 1997.
English descriptors
- KwdEn :
- Barendse, Bovine, Bovine chromosome, Bovine linkage, Cell genet, Chromosomal, Chromosome, Clone, Comparative gene mapping, Comparative linkage, Comparative linkage mapping, Female rate, Flt1, Gene, Gene order, Genet, Genetic linkage, Genetics computer group, Geno, Genome, Genomics, Gnma, Htr2a, Human chromosome, Human genome, Linkage, Linkage analysis, Linkage information, Locus, Marker, Marker development, Microsatellite, Microsatellite markers, Microsatellites, Primer, Rearrangement, Recombination, Recombination frequencies, Recombination frequency, Retinoblastoma susceptibility gene, Sequence information, Syntenic, Synteny group, Tyrosine kinase, Womack.
- Teeft :
- Barendse, Bovine, Bovine chromosome, Bovine linkage, Cell genet, Chromosomal, Chromosome, Clone, Comparative gene mapping, Comparative linkage, Comparative linkage mapping, Female rate, Flt1, Gene, Gene order, Genet, Genetic linkage, Genetics computer group, Geno, Genome, Genomics, Gnma, Htr2a, Human chromosome, Human genome, Linkage, Linkage analysis, Linkage information, Locus, Marker, Marker development, Microsatellite, Microsatellite markers, Microsatellites, Primer, Rearrangement, Recombination, Recombination frequencies, Recombination frequency, Retinoblastoma susceptibility gene, Sequence information, Syntenic, Synteny group, Tyrosine kinase, Womack.
Abstract
Abstract: A comparative linkage map of human chromosome 13 and bovine chromosome 12 was constructed using eight polymorphic microsatellite markers associated with six specific genes. Linkage of these was also examined relative to five previously mapped anonymous microsatellite markers. Seven gene-linked markers were developed from bovine large-insert genomic clones containing one of five genes of interest (serotonin receptor subtype 2, fms-related tyrosine kinase, coagulation factor 10, retinoblastoma susceptibility gene, collagen type IV alpha 1), and one additional marker was developed from a microsatellite resident within an intron of the bovine dopachrome tautomerase gene. Four of these loci were previously assigned to bovine chromosome 12 by analysis of a somatic cell hybrid panel. This study provides linkage information for examining gene order in this conserved synteny group. The comparative linkage mapping results indicate that the q arm of human chromosome 13 is almost entirely conserved in bovine chromosome 12. One intrachromosomal rearrangement was detected in this linkage group relative to human, and this rearrangement was confirmed by fluorescencein situhybridization results.
Url:
DOI: 10.1006/geno.1996.4481
Links to Exploration step
ISTEX:449D65517AF736073F97D088749C0CDFEC2C6A56Le document en format XML
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Sun</name><affiliation><mods:affiliation>Department of Animal Sciences, University of Wisconsin, Madison, Wisconsin, 53706</mods:affiliation></affiliation></author><author><name sortKey="Cai, L" sort="Cai, L" uniqKey="Cai L" first="L." last="Cai">L. Cai</name><affiliation><mods:affiliation>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</mods:affiliation></affiliation></author><author><name sortKey="Davis, S K" sort="Davis, S K" uniqKey="Davis S" first="S. K." last="Davis">S. K. Davis</name><affiliation><mods:affiliation>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</mods:affiliation></affiliation></author><author><name sortKey="Taylor, J F" sort="Taylor, J F" uniqKey="Taylor J" first="J. F." last="Taylor">J. F. 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Kirkpatrick</name><affiliation><mods:affiliation>Department of Animal Sciences, University of Wisconsin, Madison, Wisconsin, 53706</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Genomics</title><title level="j" type="abbrev">YGENO</title><idno type="ISSN">0888-7543</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1997">1997</date><biblScope unit="volume">39</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="47">47</biblScope><biblScope unit="page" to="54">54</biblScope></imprint><idno type="ISSN">0888-7543</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0888-7543</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Barendse</term><term>Bovine</term><term>Bovine chromosome</term><term>Bovine linkage</term><term>Cell genet</term><term>Chromosomal</term><term>Chromosome</term><term>Clone</term><term>Comparative gene mapping</term><term>Comparative linkage</term><term>Comparative linkage mapping</term><term>Female rate</term><term>Flt1</term><term>Gene</term><term>Gene order</term><term>Genet</term><term>Genetic linkage</term><term>Genetics computer group</term><term>Geno</term><term>Genome</term><term>Genomics</term><term>Gnma</term><term>Htr2a</term><term>Human chromosome</term><term>Human genome</term><term>Linkage</term><term>Linkage analysis</term><term>Linkage information</term><term>Locus</term><term>Marker</term><term>Marker development</term><term>Microsatellite</term><term>Microsatellite markers</term><term>Microsatellites</term><term>Primer</term><term>Rearrangement</term><term>Recombination</term><term>Recombination frequencies</term><term>Recombination frequency</term><term>Retinoblastoma susceptibility gene</term><term>Sequence information</term><term>Syntenic</term><term>Synteny group</term><term>Tyrosine kinase</term><term>Womack</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Barendse</term><term>Bovine</term><term>Bovine chromosome</term><term>Bovine linkage</term><term>Cell genet</term><term>Chromosomal</term><term>Chromosome</term><term>Clone</term><term>Comparative gene mapping</term><term>Comparative linkage</term><term>Comparative linkage mapping</term><term>Female rate</term><term>Flt1</term><term>Gene</term><term>Gene order</term><term>Genet</term><term>Genetic linkage</term><term>Genetics computer group</term><term>Geno</term><term>Genome</term><term>Genomics</term><term>Gnma</term><term>Htr2a</term><term>Human chromosome</term><term>Human genome</term><term>Linkage</term><term>Linkage analysis</term><term>Linkage information</term><term>Locus</term><term>Marker</term><term>Marker development</term><term>Microsatellite</term><term>Microsatellite markers</term><term>Microsatellites</term><term>Primer</term><term>Rearrangement</term><term>Recombination</term><term>Recombination frequencies</term><term>Recombination frequency</term><term>Retinoblastoma susceptibility gene</term><term>Sequence information</term><term>Syntenic</term><term>Synteny group</term><term>Tyrosine kinase</term><term>Womack</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: A comparative linkage map of human chromosome 13 and bovine chromosome 12 was constructed using eight polymorphic microsatellite markers associated with six specific genes. Linkage of these was also examined relative to five previously mapped anonymous microsatellite markers. Seven gene-linked markers were developed from bovine large-insert genomic clones containing one of five genes of interest (serotonin receptor subtype 2, fms-related tyrosine kinase, coagulation factor 10, retinoblastoma susceptibility gene, collagen type IV alpha 1), and one additional marker was developed from a microsatellite resident within an intron of the bovine dopachrome tautomerase gene. Four of these loci were previously assigned to bovine chromosome 12 by analysis of a somatic cell hybrid panel. This study provides linkage information for examining gene order in this conserved synteny group. The comparative linkage mapping results indicate that the q arm of human chromosome 13 is almost entirely conserved in bovine chromosome 12. One intrachromosomal rearrangement was detected in this linkage group relative to human, and this rearrangement was confirmed by fluorescencein situhybridization results.</div></front></TEI><istex><corpusName>elsevier</corpusName><keywords><teeft><json:string>chromosome</json:string><json:string>recombination</json:string><json:string>genome</json:string><json:string>clone</json:string><json:string>flt1</json:string><json:string>primer</json:string><json:string>genet</json:string><json:string>htr2a</json:string><json:string>bovine chromosome</json:string><json:string>microsatellite</json:string><json:string>bovine</json:string><json:string>rearrangement</json:string><json:string>human chromosome</json:string><json:string>womack</json:string><json:string>syntenic</json:string><json:string>barendse</json:string><json:string>linkage</json:string><json:string>geno</json:string><json:string>gnma</json:string><json:string>genomics</json:string><json:string>recombination frequency</json:string><json:string>microsatellites</json:string><json:string>linkage analysis</json:string><json:string>chromosomal</json:string><json:string>locus</json:string><json:string>gene order</json:string><json:string>microsatellite markers</json:string><json:string>cell genet</json:string><json:string>recombination frequencies</json:string><json:string>human genome</json:string><json:string>bovine linkage</json:string><json:string>linkage information</json:string><json:string>marker</json:string><json:string>tyrosine kinase</json:string><json:string>genetics computer group</json:string><json:string>comparative linkage</json:string><json:string>retinoblastoma susceptibility gene</json:string><json:string>marker development</json:string><json:string>sequence information</json:string><json:string>synteny group</json:string><json:string>female rate</json:string><json:string>genetic linkage</json:string><json:string>comparative linkage mapping</json:string><json:string>comparative gene mapping</json:string><json:string>gene</json:string></teeft></keywords><author><json:item><name>H.S. Sun</name><affiliations><json:string>Department of Animal Sciences, University of Wisconsin, Madison, Wisconsin, 53706</json:string></affiliations></json:item><json:item><name>L. Cai</name><affiliations><json:string>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</json:string></affiliations></json:item><json:item><name>S.K. Davis</name><affiliations><json:string>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</json:string></affiliations></json:item><json:item><name>J.F. Taylor</name><affiliations><json:string>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</json:string></affiliations></json:item><json:item><name>L.K. Doud</name><affiliations><json:string>ABS Global Inc. DeForest, Wisconsin, 53532</json:string></affiliations></json:item><json:item><name>M.D. Bishop</name><affiliations><json:string>ABS Global Inc. DeForest, Wisconsin, 53532</json:string></affiliations></json:item><json:item><name>H. Hayes</name><affiliations><json:string>INRA, Laboratoire de Genetique Biochimique et de Cytogenetique, Jouy-en-Josas, France</json:string></affiliations></json:item><json:item><name>W. Barendse</name><affiliations><json:string>CSIRO, Division of Tropical Animal Production, University of Queensland, Queensland, 4072, Australia</json:string></affiliations></json:item><json:item><name>D. Vaiman</name><affiliations><json:string>INRA, Laboratoire de Genetique Biochimique et de Cytogenetique, Jouy-en-Josas, France</json:string></affiliations></json:item><json:item><name>R.A. McGraw</name><affiliations><json:string>College of Veterinary Medicine, University of Georgia, Athens, Georgia, 30601</json:string></affiliations></json:item><json:item><name>T. Hirano</name><affiliations><json:string>Shirakawa Institute of Animal Genetics, Fukushima, Japan</json:string></affiliations></json:item><json:item><name>Y. Sugimoto</name><affiliations><json:string>Shirakawa Institute of Animal Genetics, Fukushima, Japan</json:string></affiliations></json:item><json:item><name>B.W. Kirkpatrick</name><affiliations><json:string>Department of Animal Sciences, University of Wisconsin, Madison, Wisconsin, 53706</json:string></affiliations></json:item></author><arkIstex>ark:/67375/6H6-4JRQ14DM-7</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>Abstract: A comparative linkage map of human chromosome 13 and bovine chromosome 12 was constructed using eight polymorphic microsatellite markers associated with six specific genes. Linkage of these was also examined relative to five previously mapped anonymous microsatellite markers. Seven gene-linked markers were developed from bovine large-insert genomic clones containing one of five genes of interest (serotonin receptor subtype 2, fms-related tyrosine kinase, coagulation factor 10, retinoblastoma susceptibility gene, collagen type IV alpha 1), and one additional marker was developed from a microsatellite resident within an intron of the bovine dopachrome tautomerase gene. Four of these loci were previously assigned to bovine chromosome 12 by analysis of a somatic cell hybrid panel. This study provides linkage information for examining gene order in this conserved synteny group. The comparative linkage mapping results indicate that the q arm of human chromosome 13 is almost entirely conserved in bovine chromosome 12. One intrachromosomal rearrangement was detected in this linkage group relative to human, and this rearrangement was confirmed by fluorescencein situhybridization results.</abstract><qualityIndicators><refBibsNative>false</refBibsNative><abstractWordCount>169</abstractWordCount><abstractCharCount>1207</abstractCharCount><keywordCount>0</keywordCount><score>9.028</score><pdfWordCount>5351</pdfWordCount><pdfCharCount>33845</pdfCharCount><pdfVersion>1.1</pdfVersion><pdfPageCount>8</pdfPageCount><pdfPageSize>540 x 720 pts</pdfPageSize></qualityIndicators><title>Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12</title><pmid><json:string>9027485</json:string></pmid><pii><json:string>S0888-7543(96)94481-X</json:string></pii><genre><json:string>research-article</json:string></genre><host><title>Genomics</title><language><json:string>unknown</json:string></language><publicationDate>1997</publicationDate><issn><json:string>0888-7543</json:string></issn><pii><json:string>S0888-7543(00)X0106-1</json:string></pii><volume>39</volume><issue>1</issue><pages><first>47</first><last>54</last></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>1997</json:string><json:string>12S</json:string></date><geogName></geogName><orgName><json:string>University of Georgia, Athens, Georgia</json:string><json:string>University of Queensland</json:string><json:string>Department of Animal Science, Texas A</json:string><json:string>University of Wisconsin</json:string><json:string>ABS Global, Inc.</json:string><json:string>Shirakawa Institute of Animal Genetics, Fukushima, Japan Received</json:string><json:string>Biochem</json:string><json:string>Division of Tropical Animal Production</json:string><json:string>ABS Global Inc.</json:string><json:string>USDA Grant 93-01546</json:string><json:string>Hatch Project</json:string></orgName><orgName_funder><json:string>USDA Grant 93-01546</json:string><json:string>Hatch Project</json:string></orgName_funder><orgName_provider></orgName_provider><persName><json:string>Yvonne Moll</json:string><json:string>Andre Eggen</json:string><json:string>Jeff Popp</json:string><json:string>Sonja Dimintrijevic</json:string><json:string>Niels J. Larsen</json:string><json:string>W. Barendse</json:string><json:string>Van de Weghe</json:string></persName><placeName><json:string>Foster City</json:string><json:string>San Diego</json:string><json:string>Madison</json:string><json:string>CA</json:string><json:string>LOD</json:string><json:string>France</json:string><json:string>WI</json:string><json:string>Cambridge</json:string></placeName><ref_url><json:string>http://cedar.genetics.soton.ac.uk/ public_html/</json:string></ref_url><ref_bibl><json:string>Green and Olson, 1990</json:string><json:string>Hayes et al., 1992</json:string><json:string>Morton et al., 1992</json:string><json:string>Bouchard et al., 1994</json:string><json:string>Libert et al., 1993</json:string><json:string>Hayes et al. (1993)</json:string><json:string>Washington et al. (1995)</json:string><json:string>Hayes, 1995</json:string><json:string>DiBeradino et al., 1990</json:string><json:string>Brien et al., 1993a,b</json:string><json:string>Lenstra et al. 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(1993)</json:string><json:string>Green et al., 1990</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/6H6-4JRQ14DM-7</json:string></ark><categories><wos><json:string>1 - science</json:string><json:string>2 - genetics & heredity</json:string><json:string>2 - biotechnology & applied microbiology</json:string></wos><scienceMetrix><json:string>1 - health sciences</json:string><json:string>2 - biomedical research</json:string><json:string>3 - genetics & heredity</json:string></scienceMetrix><scopus><json:string>1 - Life Sciences</json:string><json:string>2 - Biochemistry, Genetics and Molecular Biology</json:string><json:string>3 - Genetics</json:string></scopus><inist><json:string>1 - sciences appliquees, technologies et medecines</json:string><json:string>2 - sciences biologiques et medicales</json:string><json:string>3 - sciences biologiques fondamentales et appliquees. psychologie</json:string><json:string>4 - genetique des eucaryotes. evolution biologique et moleculaire</json:string></inist></categories><publicationDate>1997</publicationDate><copyrightDate>1997</copyrightDate><doi><json:string>10.1006/geno.1996.4481</json:string></doi><id>449D65517AF736073F97D088749C0CDFEC2C6A56</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/449D65517AF736073F97D088749C0CDFEC2C6A56/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/449D65517AF736073F97D088749C0CDFEC2C6A56/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/449D65517AF736073F97D088749C0CDFEC2C6A56/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12</title><respStmt><resp>Références bibliographiques récupérées via GROBID</resp><name resp="ISTEX-API">ISTEX-API (INIST-CNRS)</name></respStmt></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>ELSEVIER</publisher><availability><p>©1997 Academic Press</p></availability><date>1997</date></publicationStmt><notesStmt><note>Sequence data from this article have been deposited with the GenBank/EMBL Data Libraries under Accession Nos. U39264–U39267 and U47656–U47659.</note><note type="content">Section title: Regular Article</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12</title><author xml:id="author-0000"><persName><forename type="first">H.S.</forename><surname>Sun</surname></persName><affiliation>Department of Animal Sciences, University of Wisconsin, Madison, Wisconsin, 53706</affiliation></author><author xml:id="author-0001"><persName><forename type="first">L.</forename><surname>Cai</surname></persName><affiliation>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</affiliation></author><author xml:id="author-0002"><persName><forename type="first">S.K.</forename><surname>Davis</surname></persName><affiliation>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</affiliation></author><author xml:id="author-0003"><persName><forename type="first">J.F.</forename><surname>Taylor</surname></persName><affiliation>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</affiliation></author><author xml:id="author-0004"><persName><forename type="first">L.K.</forename><surname>Doud</surname></persName><affiliation>ABS Global Inc. DeForest, Wisconsin, 53532</affiliation></author><author xml:id="author-0005"><persName><forename type="first">M.D.</forename><surname>Bishop</surname></persName><affiliation>ABS Global Inc. DeForest, Wisconsin, 53532</affiliation></author><author xml:id="author-0006"><persName><forename type="first">H.</forename><surname>Hayes</surname></persName><affiliation>INRA, Laboratoire de Genetique Biochimique et de Cytogenetique, Jouy-en-Josas, France</affiliation></author><author xml:id="author-0007"><persName><forename type="first">W.</forename><surname>Barendse</surname></persName><affiliation>CSIRO, Division of Tropical Animal Production, University of Queensland, Queensland, 4072, Australia</affiliation></author><author xml:id="author-0008"><persName><forename type="first">D.</forename><surname>Vaiman</surname></persName><affiliation>INRA, Laboratoire de Genetique Biochimique et de Cytogenetique, Jouy-en-Josas, France</affiliation></author><author xml:id="author-0009"><persName><forename type="first">R.A.</forename><surname>McGraw</surname></persName><affiliation>College of Veterinary Medicine, University of Georgia, Athens, Georgia, 30601</affiliation></author><author xml:id="author-0010"><persName><forename type="first">T.</forename><surname>Hirano</surname></persName><affiliation>Shirakawa Institute of Animal Genetics, Fukushima, Japan</affiliation></author><author xml:id="author-0011"><persName><forename type="first">Y.</forename><surname>Sugimoto</surname></persName><affiliation>Shirakawa Institute of Animal Genetics, Fukushima, Japan</affiliation></author><author xml:id="author-0012"><persName><forename type="first">B.W.</forename><surname>Kirkpatrick</surname></persName><affiliation>Department of Animal Sciences, University of Wisconsin, Madison, Wisconsin, 53706</affiliation></author><idno type="istex">449D65517AF736073F97D088749C0CDFEC2C6A56</idno><idno type="DOI">10.1006/geno.1996.4481</idno><idno type="PII">S0888-7543(96)94481-X</idno></analytic><monogr><title level="j">Genomics</title><title level="j" type="abbrev">YGENO</title><idno type="pISSN">0888-7543</idno><idno type="PII">S0888-7543(00)X0106-1</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1997"></date><biblScope unit="volume">39</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="47">47</biblScope><biblScope unit="page" to="54">54</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1997</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>A comparative linkage map of human chromosome 13 and bovine chromosome 12 was constructed using eight polymorphic microsatellite markers associated with six specific genes. Linkage of these was also examined relative to five previously mapped anonymous microsatellite markers. Seven gene-linked markers were developed from bovine large-insert genomic clones containing one of five genes of interest (serotonin receptor subtype 2, fms-related tyrosine kinase, coagulation factor 10, retinoblastoma susceptibility gene, collagen type IV alpha 1), and one additional marker was developed from a microsatellite resident within an intron of the bovine dopachrome tautomerase gene. Four of these loci were previously assigned to bovine chromosome 12 by analysis of a somatic cell hybrid panel. This study provides linkage information for examining gene order in this conserved synteny group. The comparative linkage mapping results indicate that the q arm of human chromosome 13 is almost entirely conserved in bovine chromosome 12. One intrachromosomal rearrangement was detected in this linkage group relative to human, and this rearrangement was confirmed by fluorescencein situhybridization results.</p></abstract></profileDesc><revisionDesc><change when="1997">Published</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2017-09-30">References added</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/449D65517AF736073F97D088749C0CDFEC2C6A56/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier converted-article found"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla" xml:lang="en"><item-info><jid>YGENO</jid><aid>94481</aid><ce:pii>S0888-7543(96)94481-X</ce:pii><ce:doi>10.1006/geno.1996.4481</ce:doi><ce:copyright type="full-transfer" year="1997">Academic Press</ce:copyright></item-info><head><ce:article-footnote><ce:label>☆</ce:label><ce:note-para>Sequence data from this article have been deposited with the GenBank/EMBL Data Libraries under Accession Nos. U39264–U39267 and U47656–U47659.</ce:note-para></ce:article-footnote><ce:dochead><ce:textfn>Regular Article</ce:textfn></ce:dochead><ce:title>Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12</ce:title><ce:author-group><ce:author><ce:given-name>H.S.</ce:given-name><ce:surname>Sun</ce:surname><ce:cross-ref refid="GE964481A1"><ce:sup>a</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>L.</ce:given-name><ce:surname>Cai</ce:surname><ce:cross-ref refid="GE964481A2"><ce:sup>b</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>S.K.</ce:given-name><ce:surname>Davis</ce:surname><ce:cross-ref refid="GE964481A2"><ce:sup>b</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>J.F.</ce:given-name><ce:surname>Taylor</ce:surname><ce:cross-ref refid="GE964481A2"><ce:sup>b</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>L.K.</ce:given-name><ce:surname>Doud</ce:surname><ce:cross-ref refid="GE964481A3"><ce:sup>c</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>M.D.</ce:given-name><ce:surname>Bishop</ce:surname><ce:cross-ref refid="GE964481A3"><ce:sup>c</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>H.</ce:given-name><ce:surname>Hayes</ce:surname><ce:cross-ref refid="GE964481A4"><ce:sup>d</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>W.</ce:given-name><ce:surname>Barendse</ce:surname><ce:cross-ref refid="GE964481A5"><ce:sup>e</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>D.</ce:given-name><ce:surname>Vaiman</ce:surname><ce:cross-ref refid="GE964481A4"><ce:sup>d</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>R.A.</ce:given-name><ce:surname>McGraw</ce:surname><ce:cross-ref refid="GE964481A6"><ce:sup>f</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>T.</ce:given-name><ce:surname>Hirano</ce:surname><ce:cross-ref refid="GE964481A7"><ce:sup>g</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Y.</ce:given-name><ce:surname>Sugimoto</ce:surname><ce:cross-ref refid="GE964481A7"><ce:sup>g</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>B.W.</ce:given-name><ce:surname>Kirkpatrick</ce:surname><ce:cross-ref refid="GE964481A1"><ce:sup>a</ce:sup></ce:cross-ref><ce:cross-ref refid="GE964481FN1">1</ce:cross-ref></ce:author><ce:affiliation id="GE964481A1"><ce:label>a</ce:label><ce:textfn>Department of Animal Sciences, University of Wisconsin, Madison, Wisconsin, 53706</ce:textfn></ce:affiliation><ce:affiliation id="GE964481A2"><ce:label>b</ce:label><ce:textfn>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</ce:textfn></ce:affiliation><ce:affiliation id="GE964481A3"><ce:label>c</ce:label><ce:textfn>ABS Global Inc. DeForest, Wisconsin, 53532</ce:textfn></ce:affiliation><ce:affiliation id="GE964481A5"><ce:label>e</ce:label><ce:textfn>CSIRO, Division of Tropical Animal Production, University of Queensland, Queensland, 4072, Australia</ce:textfn></ce:affiliation><ce:affiliation id="GE964481A4"><ce:label>d</ce:label><ce:textfn>INRA, Laboratoire de Genetique Biochimique et de Cytogenetique, Jouy-en-Josas, France</ce:textfn></ce:affiliation><ce:affiliation id="GE964481A6"><ce:label>f</ce:label><ce:textfn>College of Veterinary Medicine, University of Georgia, Athens, Georgia, 30601</ce:textfn></ce:affiliation><ce:affiliation id="GE964481A7"><ce:label>g</ce:label><ce:textfn>Shirakawa Institute of Animal Genetics, Fukushima, Japan</ce:textfn></ce:affiliation><ce:footnote id="GE964481FN1"><ce:label>1</ce:label><ce:note-para>To whom correspondence should be addressed at Department of Animal Sciences, University of Wisconsin-Madison, 1675 Observatory Drive, Madison, WI 53706. Telephone: (608) 263-4323. Fax: (608) 262-5157. E-mail: kirkpat@calshp.cals.wisc.edu.</ce:note-para></ce:footnote></ce:author-group><ce:date-received day="26" month="6" year="1996"></ce:date-received><ce:date-accepted day="30" month="10" year="1996"></ce:date-accepted><ce:abstract><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para>A comparative linkage map of human chromosome 13 and bovine chromosome 12 was constructed using eight polymorphic microsatellite markers associated with six specific genes. Linkage of these was also examined relative to five previously mapped anonymous microsatellite markers. Seven gene-linked markers were developed from bovine large-insert genomic clones containing one of five genes of interest (serotonin receptor subtype 2, fms-related tyrosine kinase, coagulation factor 10, retinoblastoma susceptibility gene, collagen type IV alpha 1), and one additional marker was developed from a microsatellite resident within an intron of the bovine dopachrome tautomerase gene. Four of these loci were previously assigned to bovine chromosome 12 by analysis of a somatic cell hybrid panel. This study provides linkage information for examining gene order in this conserved synteny group. The comparative linkage mapping results indicate that the q arm of human chromosome 13 is almost entirely conserved in bovine chromosome 12. One intrachromosomal rearrangement was detected in this linkage group relative to human, and this rearrangement was confirmed by fluorescence<ce:italic>in situ</ce:italic>hybridization results.</ce:simple-para></ce:abstract-sec></ce:abstract></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12</title></titleInfo><titleInfo type="alternative" lang="en" contentType="CDATA"><title>Comparative Linkage Mapping of Human Chromosome 13 and Bovine Chromosome 12</title></titleInfo><name type="personal"><namePart type="given">H.S.</namePart><namePart type="family">Sun</namePart><affiliation>Department of Animal Sciences, University of Wisconsin, Madison, Wisconsin, 53706</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">L.</namePart><namePart type="family">Cai</namePart><affiliation>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S.K.</namePart><namePart type="family">Davis</namePart><affiliation>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">J.F.</namePart><namePart type="family">Taylor</namePart><affiliation>Department of Animal Science, Texas A&M University, College Station, Texas, 77843</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">L.K.</namePart><namePart type="family">Doud</namePart><affiliation>ABS Global Inc. DeForest, Wisconsin, 53532</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M.D.</namePart><namePart type="family">Bishop</namePart><affiliation>ABS Global Inc. DeForest, Wisconsin, 53532</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H.</namePart><namePart type="family">Hayes</namePart><affiliation>INRA, Laboratoire de Genetique Biochimique et de Cytogenetique, Jouy-en-Josas, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">W.</namePart><namePart type="family">Barendse</namePart><affiliation>CSIRO, Division of Tropical Animal Production, University of Queensland, Queensland, 4072, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">D.</namePart><namePart type="family">Vaiman</namePart><affiliation>INRA, Laboratoire de Genetique Biochimique et de Cytogenetique, Jouy-en-Josas, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">R.A.</namePart><namePart type="family">McGraw</namePart><affiliation>College of Veterinary Medicine, University of Georgia, Athens, Georgia, 30601</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T.</namePart><namePart type="family">Hirano</namePart><affiliation>Shirakawa Institute of Animal Genetics, Fukushima, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y.</namePart><namePart type="family">Sugimoto</namePart><affiliation>Shirakawa Institute of Animal Genetics, Fukushima, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">B.W.</namePart><namePart type="family">Kirkpatrick</namePart><affiliation>Department of Animal Sciences, University of Wisconsin, Madison, Wisconsin, 53706</affiliation><description>To whom correspondence should be addressed at Department of Animal Sciences, University of Wisconsin-Madison, 1675 Observatory Drive, Madison, WI 53706. Telephone: (608) 263-4323. Fax: (608) 262-5157. E-mail: kirkpat@calshp.cals.wisc.edu.</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1997</dateIssued><copyrightDate encoding="w3cdtf">1997</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><abstract lang="en">Abstract: A comparative linkage map of human chromosome 13 and bovine chromosome 12 was constructed using eight polymorphic microsatellite markers associated with six specific genes. Linkage of these was also examined relative to five previously mapped anonymous microsatellite markers. Seven gene-linked markers were developed from bovine large-insert genomic clones containing one of five genes of interest (serotonin receptor subtype 2, fms-related tyrosine kinase, coagulation factor 10, retinoblastoma susceptibility gene, collagen type IV alpha 1), and one additional marker was developed from a microsatellite resident within an intron of the bovine dopachrome tautomerase gene. Four of these loci were previously assigned to bovine chromosome 12 by analysis of a somatic cell hybrid panel. This study provides linkage information for examining gene order in this conserved synteny group. The comparative linkage mapping results indicate that the q arm of human chromosome 13 is almost entirely conserved in bovine chromosome 12. One intrachromosomal rearrangement was detected in this linkage group relative to human, and this rearrangement was confirmed by fluorescencein situhybridization results.</abstract><note>Sequence data from this article have been deposited with the GenBank/EMBL Data Libraries under Accession Nos. 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