A linkage map of sweet cherry based on RAPD analysis of a microspore-derived callus culture population
A partial linkage map was constructed for the sweet cherry (Prunus avium L.) cultivar Emperor Francis from a population of 56 microspore-derived callus culture individuals. The callus cultures were genotyped for two allozymes and 90 random amplified polymorphic DNA(RAPD) markers using 79 random deca...
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| Veröffentlicht in: | The Journal of heredity 1996-05, Vol.87 (3), p.214-218 |
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| container_title | The Journal of heredity |
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| creator | Stockinger, E.J. (Michigan State University, East Lansing, MI.) Mulinix, C.A Long, C.M Brettin, T.S Iezzoni, A.F |
| description | A partial linkage map was constructed for the sweet cherry (Prunus avium L.) cultivar Emperor Francis from a population of 56 microspore-derived callus culture individuals. The callus cultures were genotyped for two allozymes and 90 random amplified polymorphic DNA(RAPD) markers using 79 random decanucleotide DNA primers and the polymerase chain reaction (PCR). Eighty-nine markers mapped to 10 linkage groups totaling 503.3 cM. DNA blot and hybridization analysis using five cloned RAPDs as probes demonstrated that one of the decanucleotide primers amplified a region of the Emperor Francis genome containing a unique sequence, whereas the other four decanucleotide primers amplified regions of the Emperor Francis genome containing repeated sequences. The five cloned RAPD probes also recognized putative homologous regions in ground cherry, P. fruticosa Pall., and sour cherry, P. cerasus L., a naturally occurring allopolyploid between P. fruticosa and P. avium |
| doi_str_mv | 10.1093/oxfordjournals.jhered.a022987 |
| format | Article |
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(Michigan State University, East Lansing, MI.) ; Mulinix, C.A ; Long, C.M ; Brettin, T.S ; Iezzoni, A.F</creator><creatorcontrib>Stockinger, E.J. (Michigan State University, East Lansing, MI.) ; Mulinix, C.A ; Long, C.M ; Brettin, T.S ; Iezzoni, A.F</creatorcontrib><description>A partial linkage map was constructed for the sweet cherry (Prunus avium L.) cultivar Emperor Francis from a population of 56 microspore-derived callus culture individuals. The callus cultures were genotyped for two allozymes and 90 random amplified polymorphic DNA(RAPD) markers using 79 random decanucleotide DNA primers and the polymerase chain reaction (PCR). Eighty-nine markers mapped to 10 linkage groups totaling 503.3 cM. DNA blot and hybridization analysis using five cloned RAPDs as probes demonstrated that one of the decanucleotide primers amplified a region of the Emperor Francis genome containing a unique sequence, whereas the other four decanucleotide primers amplified regions of the Emperor Francis genome containing repeated sequences. The five cloned RAPD probes also recognized putative homologous regions in ground cherry, P. fruticosa Pall., and sour cherry, P. cerasus L., a naturally occurring allopolyploid between P. fruticosa and P. avium</description><identifier>ISSN: 0022-1503</identifier><identifier>EISSN: 1465-7333</identifier><identifier>EISSN: 1471-8505</identifier><identifier>DOI: 10.1093/oxfordjournals.jhered.a022987</identifier><identifier>PMID: 8683097</identifier><identifier>CODEN: JOHEA8</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>ADN ; Base Sequence ; CAL ; CALLO ; Chromosome Mapping ; CLONE ; CLONES ; Cloning, Molecular ; CULTIVO DE TEJIDOS ; CULTURE DE TISSU ; Culture Techniques ; Deoxyribonucleic acid ; DNA ; DNA, Plant ; ENZIMAS ; ENZYME ; Flowers & plants ; Fruit - genetics ; Fruits ; GENE ; GENES ; Genetic Linkage ; Genetic Markers ; Genetics ; Genome, Plant ; HIBRIDACION DE ADN ; HYBRIDATION D'ADN ; MARCADORES GENETICOS ; MARQUEUR GENETIQUE ; Molecular Sequence Data ; PCR ; PRUNUS ; PRUNUS AVIUM ; PRUNUS CERASUS ; Prunus fruticosa ; Random Amplified Polymorphic DNA Technique ; SECUENCIA NUCLEOTIDICA ; SEQUENCE NUCLEOTIDIQUE</subject><ispartof>The Journal of heredity, 1996-05, Vol.87 (3), p.214-218</ispartof><rights>Copyright Oxford University Press(England) May 1996</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-15f64a00c39e583f8e3df7d6091d407e551d93c7d26dc52038868dedb995dcea3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8683097$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stockinger, E.J. (Michigan State University, East Lansing, MI.)</creatorcontrib><creatorcontrib>Mulinix, C.A</creatorcontrib><creatorcontrib>Long, C.M</creatorcontrib><creatorcontrib>Brettin, T.S</creatorcontrib><creatorcontrib>Iezzoni, A.F</creatorcontrib><title>A linkage map of sweet cherry based on RAPD analysis of a microspore-derived callus culture population</title><title>The Journal of heredity</title><addtitle>J Hered</addtitle><description>A partial linkage map was constructed for the sweet cherry (Prunus avium L.) cultivar Emperor Francis from a population of 56 microspore-derived callus culture individuals. The callus cultures were genotyped for two allozymes and 90 random amplified polymorphic DNA(RAPD) markers using 79 random decanucleotide DNA primers and the polymerase chain reaction (PCR). Eighty-nine markers mapped to 10 linkage groups totaling 503.3 cM. DNA blot and hybridization analysis using five cloned RAPDs as probes demonstrated that one of the decanucleotide primers amplified a region of the Emperor Francis genome containing a unique sequence, whereas the other four decanucleotide primers amplified regions of the Emperor Francis genome containing repeated sequences. The five cloned RAPD probes also recognized putative homologous regions in ground cherry, P. fruticosa Pall., and sour cherry, P. cerasus L., a naturally occurring allopolyploid between P. fruticosa and P. avium</description><subject>ADN</subject><subject>Base Sequence</subject><subject>CAL</subject><subject>CALLO</subject><subject>Chromosome Mapping</subject><subject>CLONE</subject><subject>CLONES</subject><subject>Cloning, Molecular</subject><subject>CULTIVO DE TEJIDOS</subject><subject>CULTURE DE TISSU</subject><subject>Culture Techniques</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA, Plant</subject><subject>ENZIMAS</subject><subject>ENZYME</subject><subject>Flowers & plants</subject><subject>Fruit - genetics</subject><subject>Fruits</subject><subject>GENE</subject><subject>GENES</subject><subject>Genetic Linkage</subject><subject>Genetic Markers</subject><subject>Genetics</subject><subject>Genome, Plant</subject><subject>HIBRIDACION DE ADN</subject><subject>HYBRIDATION D'ADN</subject><subject>MARCADORES GENETICOS</subject><subject>MARQUEUR GENETIQUE</subject><subject>Molecular Sequence Data</subject><subject>PCR</subject><subject>PRUNUS</subject><subject>PRUNUS AVIUM</subject><subject>PRUNUS CERASUS</subject><subject>Prunus fruticosa</subject><subject>Random Amplified Polymorphic DNA Technique</subject><subject>SECUENCIA NUCLEOTIDICA</subject><subject>SEQUENCE NUCLEOTIDIQUE</subject><issn>0022-1503</issn><issn>1465-7333</issn><issn>1471-8505</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS0EKkvhDyAhWUhwyzKOYzs-cFi1lCJVBcFWQlwsbzwp2SZxaifQ_fd4lS0SXHqyNPO9mTd-hLxhsGSg-Tt_V_vgtn4KvW3jcvsTA7qlhTzXpXpEFqyQIlOc88dkAamaMQH8KXkW4xYAmNBwRI5KWXLQakHqFW2b_sZeI-3sQH1N42_EkVZpbNjRjY3oqO_p19WXU2rTxl1s4h6ztGuq4OPgA2YOQ_MrgZVt2ynSamrHKSAd_DC1dmx8_5w8qZNbfHF4j8nV2Yf1yXl28fnjp5PVRVaJnI3Jai0LC1BxjaLkdYnc1cpJ0MwVoFAI5jSvlMulSwrgZTrEodtoLVyFlh-Tt_PcIfjbCeNouiZW2La2Rz9Fo0oGUrHiQTCHgiuW8wdBJmRyxUUCX_8H3mdkmC5BSZXrBL2fof3XxYC1GULT2bAzDMw-XvNvvGaO1xziTfpXhyXTpkv1e_Uhz9TP5n4TR7z727bhxkjFlTDn33-YNSsv9en60pwl_uXM19Ybex2aaK6-aZlLSGb_AGqGv_0</recordid><startdate>19960501</startdate><enddate>19960501</enddate><creator>Stockinger, E.J. 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(Michigan State University, East Lansing, MI.)</au><au>Mulinix, C.A</au><au>Long, C.M</au><au>Brettin, T.S</au><au>Iezzoni, A.F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A linkage map of sweet cherry based on RAPD analysis of a microspore-derived callus culture population</atitle><jtitle>The Journal of heredity</jtitle><addtitle>J Hered</addtitle><date>1996-05-01</date><risdate>1996</risdate><volume>87</volume><issue>3</issue><spage>214</spage><epage>218</epage><pages>214-218</pages><issn>0022-1503</issn><eissn>1465-7333</eissn><eissn>1471-8505</eissn><coden>JOHEA8</coden><abstract>A partial linkage map was constructed for the sweet cherry (Prunus avium L.) cultivar Emperor Francis from a population of 56 microspore-derived callus culture individuals. The callus cultures were genotyped for two allozymes and 90 random amplified polymorphic DNA(RAPD) markers using 79 random decanucleotide DNA primers and the polymerase chain reaction (PCR). Eighty-nine markers mapped to 10 linkage groups totaling 503.3 cM. DNA blot and hybridization analysis using five cloned RAPDs as probes demonstrated that one of the decanucleotide primers amplified a region of the Emperor Francis genome containing a unique sequence, whereas the other four decanucleotide primers amplified regions of the Emperor Francis genome containing repeated sequences. The five cloned RAPD probes also recognized putative homologous regions in ground cherry, P. fruticosa Pall., and sour cherry, P. cerasus L., a naturally occurring allopolyploid between P. fruticosa and P. avium</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>8683097</pmid><doi>10.1093/oxfordjournals.jhered.a022987</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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| ispartof | The Journal of heredity, 1996-05, Vol.87 (3), p.214-218 |
| issn | 0022-1503 1465-7333 1471-8505 |
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| source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current) |
| subjects | ADN Base Sequence CAL CALLO Chromosome Mapping CLONE CLONES Cloning, Molecular CULTIVO DE TEJIDOS CULTURE DE TISSU Culture Techniques Deoxyribonucleic acid DNA DNA, Plant ENZIMAS ENZYME Flowers & plants Fruit - genetics Fruits GENE GENES Genetic Linkage Genetic Markers Genetics Genome, Plant HIBRIDACION DE ADN HYBRIDATION D'ADN MARCADORES GENETICOS MARQUEUR GENETIQUE Molecular Sequence Data PCR PRUNUS PRUNUS AVIUM PRUNUS CERASUS Prunus fruticosa Random Amplified Polymorphic DNA Technique SECUENCIA NUCLEOTIDICA SEQUENCE NUCLEOTIDIQUE |
| title | A linkage map of sweet cherry based on RAPD analysis of a microspore-derived callus culture population |
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