Genetic diagnosis of Rehmannia species micropropagated by tip tissue culture and an F1 hybrid by RAPD analysis
Identifieur interne : 000429 ( Istex/Corpus ); précédent : 000428; suivant : 000430Genetic diagnosis of Rehmannia species micropropagated by tip tissue culture and an F1 hybrid by RAPD analysis
Auteurs : M. Hatano ; R. Nakai ; F. Kawanishi2 ; K. Kedo2 ; Y. Shoyama1Source :
- Plant Breeding [ 0179-9541 ] ; 1997-12.
English descriptors
- Teeft :
- Clonal, Clonal multiplication, Clonal propagation, Genetic analysis, Genetic distance, Genetic distances, Genetic homogeneity, Genetie homogeneity, Glulinosa, Glutinosa, Hybrid, Hybrid strain, Iridoid glycoside contents, Kyushu university, Large amount, Medicinal plants, Micropropagation, Parental, Parental plants, Parental species, Pharmaceutical sciences, Plania mediea, Planl cell, Plant cell, Planta mediea, Plantlet, Plantlets regenerated, Primer, Purpurea, Purpurea makino, Qualitative analysis, Random primers, Rapd, Rapd analysis, Rapd markers, Regenerated, Regenerated plantlets, Rehmannia, Rehmannia glulinosa, Rehmannia species, Root division, Sample material, Secondary metabolites, Shoyama, Takeda chemical industries, Tissue culture, Tuberous roots, Typical bands, Virus infection.
Abstract
Shoot formation was induced from the tip tissue of Rehmannia glutinosa f. hueichingensis on hormone‐free Murashige‐Skoog medium within 4 weeks of culture. Shoots were propagated on Murashige‐Skoog medium supplemented with l.0mg/l benzy0ladenine for 4 weeks. Propagated shoots rooted on the hormone‐free Murashige‐Skoog medium during 4 weeks of culture. Total DNA was extracted from the leaves of a F1 hybrid and its parents. R. glulinosa f. huekliingensis and R. glutinosa var, purpurea. Analysis of random‐amplified polymorphic DNA (RAPD) using 10 arbitrary oligonucleotide 10‐mers. showed the genetic homogeneity ofthe above three species. The F1 hybrid was genetically intermediate between both parental plants, compared with the genetic distance between the F1 hybrid and individual parents. Furthermore, the comparison of the band patterns between the F1 hybrid, obtained from the crossing clearly showed that parts of the bands of both parents. R. glutinosa f. hueichingensis and R. glutinosa var. purpurea, were introduced into the F1 hybrid.
Url:
DOI: 10.1111/j.1439-0523.1997.tb02195.x
Links to Exploration step
ISTEX:8FC34F54F4B0E5F0DBFC14DAF20549370BA72A4FLe document en format XML
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Hatano</name><affiliation><mods:affiliation>Faculty of Pharmaceutical Sciences, Kyushu University, Higashiku, Fukuoka 812, Japan</mods:affiliation></affiliation></author><author><name sortKey="Nakai, R" sort="Nakai, R" uniqKey="Nakai R" first="R." last="Nakai">R. Nakai</name><affiliation><mods:affiliation>Faculty of Pharmaceutical Sciences, Kyushu University, Higashiku, Fukuoka 812, Japan</mods:affiliation></affiliation></author><author><name sortKey="Kawanishi2, F" sort="Kawanishi2, F" uniqKey="Kawanishi2 F" first="F." last="Kawanishi2">F. Kawanishi2</name><affiliation><mods:affiliation>Fukuchiyama Experitnental Farm, Takeda Chemical Industries Ltd, 4428‐2 Nagata, Fukuchiyama 620‐1, Japan</mods:affiliation></affiliation></author><author><name sortKey="Kedo2, K" sort="Kedo2, K" uniqKey="Kedo2 K" first="K." last="Kedo2">K. 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Shoyama1</name><affiliation><mods:affiliation>Faculty of Pharmaceutical Sciences, Kyushu University, Higashiku, Fukuoka 812, Japan</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Plant Breeding</title><title level="j" type="alt">PLANT BREEDING</title><idno type="ISSN">0179-9541</idno><idno type="eISSN">1439-0523</idno><imprint><biblScope unit="vol">116</biblScope><biblScope unit="issue">6</biblScope><biblScope unit="page" from="589">589</biblScope><biblScope unit="page" to="591">591</biblScope><biblScope unit="page-count">3</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="1997-12">1997-12</date></imprint><idno type="ISSN">0179-9541</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0179-9541</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Clonal</term><term>Clonal multiplication</term><term>Clonal propagation</term><term>Genetic analysis</term><term>Genetic distance</term><term>Genetic distances</term><term>Genetic homogeneity</term><term>Genetie homogeneity</term><term>Glulinosa</term><term>Glutinosa</term><term>Hybrid</term><term>Hybrid strain</term><term>Iridoid glycoside contents</term><term>Kyushu university</term><term>Large amount</term><term>Medicinal plants</term><term>Micropropagation</term><term>Parental</term><term>Parental plants</term><term>Parental species</term><term>Pharmaceutical sciences</term><term>Plania mediea</term><term>Planl cell</term><term>Plant cell</term><term>Planta mediea</term><term>Plantlet</term><term>Plantlets regenerated</term><term>Primer</term><term>Purpurea</term><term>Purpurea makino</term><term>Qualitative analysis</term><term>Random primers</term><term>Rapd</term><term>Rapd analysis</term><term>Rapd markers</term><term>Regenerated</term><term>Regenerated plantlets</term><term>Rehmannia</term><term>Rehmannia glulinosa</term><term>Rehmannia species</term><term>Root division</term><term>Sample material</term><term>Secondary metabolites</term><term>Shoyama</term><term>Takeda chemical industries</term><term>Tissue culture</term><term>Tuberous roots</term><term>Typical bands</term><term>Virus infection</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Shoot formation was induced from the tip tissue of Rehmannia glutinosa f. hueichingensis on hormone‐free Murashige‐Skoog medium within 4 weeks of culture. Shoots were propagated on Murashige‐Skoog medium supplemented with l.0mg/l benzy0ladenine for 4 weeks. Propagated shoots rooted on the hormone‐free Murashige‐Skoog medium during 4 weeks of culture. Total DNA was extracted from the leaves of a F1 hybrid and its parents. R. glulinosa f. huekliingensis and R. glutinosa var, purpurea. Analysis of random‐amplified polymorphic DNA (RAPD) using 10 arbitrary oligonucleotide 10‐mers. showed the genetic homogeneity ofthe above three species. The F1 hybrid was genetically intermediate between both parental plants, compared with the genetic distance between the F1 hybrid and individual parents. Furthermore, the comparison of the band patterns between the F1 hybrid, obtained from the crossing clearly showed that parts of the bands of both parents. R. glutinosa f. hueichingensis and R. glutinosa var. purpurea, were introduced into the F1 hybrid.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>rapd</json:string><json:string>hybrid</json:string><json:string>rehmannia</json:string><json:string>purpurea</json:string><json:string>shoyama</json:string><json:string>regenerated</json:string><json:string>plantlet</json:string><json:string>primer</json:string><json:string>rapd analysis</json:string><json:string>glutinosa</json:string><json:string>glulinosa</json:string><json:string>tissue culture</json:string><json:string>clonal</json:string><json:string>micropropagation</json:string><json:string>parental plants</json:string><json:string>parental species</json:string><json:string>qualitative analysis</json:string><json:string>medicinal plants</json:string><json:string>secondary metabolites</json:string><json:string>rehmannia species</json:string><json:string>regenerated plantlets</json:string><json:string>pharmaceutical sciences</json:string><json:string>genetic analysis</json:string><json:string>genetic homogeneity</json:string><json:string>parental</json:string><json:string>kyushu university</json:string><json:string>plantlets regenerated</json:string><json:string>takeda chemical industries</json:string><json:string>root division</json:string><json:string>clonal propagation</json:string><json:string>purpurea makino</json:string><json:string>large amount</json:string><json:string>random primers</json:string><json:string>genetic distances</json:string><json:string>hybrid strain</json:string><json:string>sample material</json:string><json:string>typical bands</json:string><json:string>tuberous roots</json:string><json:string>rehmannia glulinosa</json:string><json:string>rapd markers</json:string><json:string>genetic distance</json:string><json:string>planl cell</json:string><json:string>plant cell</json:string><json:string>clonal multiplication</json:string><json:string>planta mediea</json:string><json:string>plania mediea</json:string><json:string>virus infection</json:string><json:string>iridoid glycoside contents</json:string><json:string>genetie homogeneity</json:string></teeft></keywords><author><json:item><name>M. Hatano</name><affiliations><json:string>Faculty of Pharmaceutical Sciences, Kyushu University, Higashiku, Fukuoka 812, Japan</json:string></affiliations></json:item><json:item><name>R. Nakai</name><affiliations><json:string>Faculty of Pharmaceutical Sciences, Kyushu University, Higashiku, Fukuoka 812, Japan</json:string></affiliations></json:item><json:item><name>F. Kawanishi2</name><affiliations><json:string>Fukuchiyama Experitnental Farm, Takeda Chemical Industries Ltd, 4428‐2 Nagata, Fukuchiyama 620‐1, Japan</json:string></affiliations></json:item><json:item><name>K. Kedo2</name><affiliations><json:string>Fukuchiyama Experitnental Farm, Takeda Chemical Industries Ltd, 4428‐2 Nagata, Fukuchiyama 620‐1, Japan</json:string></affiliations></json:item><json:item><name>Y. 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Shoots were propagated on Murashige‐Skoog medium supplemented with l.0mg/l benzy0ladenine for 4 weeks. Propagated shoots rooted on the hormone‐free Murashige‐Skoog medium during 4 weeks of culture. Total DNA was extracted from the leaves of a F1 hybrid and its parents. R. glulinosa f. huekliingensis and R. glutinosa var, purpurea. Analysis of random‐amplified polymorphic DNA (RAPD) using 10 arbitrary oligonucleotide 10‐mers. showed the genetic homogeneity ofthe above three species. The F1 hybrid was genetically intermediate between both parental plants, compared with the genetic distance between the F1 hybrid and individual parents. Furthermore, the comparison of the band patterns between the F1 hybrid, obtained from the crossing clearly showed that parts of the bands of both parents. R. glutinosa f. hueichingensis and R. glutinosa var. purpurea, were introduced into the F1 hybrid.</abstract><qualityIndicators><score>6.337</score><pdfWordCount>2513</pdfWordCount><pdfCharCount>15545</pdfCharCount><pdfVersion>1.4</pdfVersion><pdfPageCount>4</pdfPageCount><pdfPageSize>579 x 838 pts</pdfPageSize><pdfWordsPerPage>628</pdfWordsPerPage><pdfText>true</pdfText><refBibsNative>true</refBibsNative><abstractWordCount>152</abstractWordCount><abstractCharCount>1049</abstractCharCount><keywordCount>5</keywordCount></qualityIndicators><title>Genetic diagnosis of Rehmannia species micropropagated by tip tissue culture and an F1 hybrid by RAPD analysis</title><genre><json:string>article</json:string></genre><host><title>Plant Breeding</title><language><json:string>unknown</json:string></language><doi><json:string>10.1111/(ISSN)1439-0523</json:string></doi><issn><json:string>0179-9541</json:string></issn><eissn><json:string>1439-0523</json:string></eissn><publisherId><json:string>PBR</json:string></publisherId><volume>116</volume><issue>6</issue><pages><first>589</first><last>591</last><total>3</total></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>10s</json:string><json:string>1997</json:string><json:string>60s</json:string><json:string>30s</json:string><json:string>19S</json:string></date><geogName></geogName><orgName><json:string>Japan Wilh</json:string><json:string>Ministry of Agriculture</json:string><json:string>Kyushu Umversily and Takeda Chemical Industries</json:string><json:string>Kyushu University</json:string><json:string>Biotech</json:string><json:string>Operon Technologies</json:string><json:string>Takeda Chemical Industries Ltd.</json:string></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName></persName><placeName><json:string>Uppsala</json:string><json:string>Japan</json:string><json:string>Sweden</json:string><json:string>Osaka</json:string></placeName><ref_url></ref_url><ref_bibl><json:string>Hatano et al. 1989</json:string><json:string>Shoyama et al, 1983</json:string><json:string>Matsumoto et al. 1988</json:string><json:string>Murashige and Skoog 1962</json:string><json:string>Shoyama et al.</json:string><json:string>Shoyama et al. 1997</json:string><json:string>Fahleson et al. 1994</json:string><json:string>Golo and Kawanishi 1991</json:string><json:string>Williams et al, 1990</json:string><json:string>Matsumoto et al.</json:string><json:string>Mizukami et al. 1993</json:string><json:string>Takemori et al. 1994</json:string><json:string>Rani et al. (1995)</json:string><json:string>Nakai et al. 1996</json:string><json:string>Yamazaki et al. 1994</json:string><json:string>Shoyama et al. 1983</json:string><json:string>Yatnada et al. 1991</json:string><json:string>Matsumoto et al. 1989</json:string><json:string>Goto and Kawanishi 1991</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/WNG-JM9DL1Z4-N</json:string></ark><categories><wos><json:string>1 - science</json:string><json:string>2 - plant sciences</json:string><json:string>2 - biotechnology & applied microbiology</json:string><json:string>2 - agronomy</json:string></wos><scienceMetrix><json:string>1 - natural sciences</json:string><json:string>2 - biology</json:string><json:string>3 - plant biology & botany</json:string></scienceMetrix><scopus><json:string>1 - Life Sciences</json:string><json:string>2 - Agricultural and Biological Sciences</json:string><json:string>3 - Plant Science</json:string><json:string>1 - Life 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<ref target="http://www.tei-c.org/">We use TEI</ref></desc></application></appInfo></encodingDesc><profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head><p>Shoot formation was induced from the tip tissue of <hi rend="italic">Rehmannia glutinosa</hi> f. <hi rend="italic">hueichingensis</hi> on hormone‐free Murashige‐Skoog medium within 4 weeks of culture. Shoots were propagated on Murashige‐Skoog medium supplemented with l.0mg/l benzy0ladenine for 4 weeks. Propagated shoots rooted on the hormone‐free Murashige‐Skoog medium during 4 weeks of culture. Total DNA was extracted from the leaves of a F<hi rend="subscript">1</hi> hybrid and its parents. <hi rend="italic">R. glulinosa</hi> f. <hi rend="italic">huekliingensis</hi> and <hi rend="italic">R. glutinosa</hi> var, <hi rend="italic">purpurea</hi>. Analysis of random‐amplified polymorphic DNA (RAPD) using 10 arbitrary oligonucleotide 10‐mers. showed the genetic homogeneity ofthe above three species. The F<hi rend="subscript">1</hi> hybrid was genetically intermediate between both parental plants, compared with the genetic distance between the F<hi rend="subscript">1</hi> hybrid and individual parents. Furthermore, the comparison of the band patterns between the F<hi rend="subscript">1</hi> hybrid, obtained from the crossing clearly showed that parts of the bands of both parents. <hi rend="italic">R. glutinosa</hi> f. <hi rend="italic">hueichingensis</hi> and <hi rend="italic">R. glutinosa</hi> var. <hi rend="italic">purpurea</hi>, were introduced into the F<hi rend="subscript">1</hi> hybrid.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1"><hi rend="italic">Rhemannia</hi> spec.</term><term xml:id="k2">clonal micropropagation</term><term xml:id="k3">F<hi rend="subscript">1</hi> hybrid</term><term xml:id="k4">genetic homogeneity</term><term xml:id="k5">RAPD analysis</term></keywords><keywords rend="tocHeading1"><term>Short Communication</term></keywords></textClass><langUsage><language ident="en"></language></langUsage></profileDesc><revisionDesc><change when="2019-12-20" who="#istex" xml:id="pub2tei">formatting</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/WNG-JM9DL1Z4-N/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Publishing Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1439-0523</doi><issn type="print">0179-9541</issn><issn type="electronic">1439-0523</issn><idGroup><id type="product" value="PBR"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="PLANT BREEDING">Plant Breeding</title></titleGroup></publicationMeta><publicationMeta level="part" position="12006"><doi origin="wiley">10.1111/pbr.1997.116.issue-6</doi><numberingGroup><numbering type="journalVolume" number="116">116</numbering><numbering type="journalIssue" number="6">6</numbering></numberingGroup><coverDate startDate="1997-12">December 1997</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="0058900" status="forIssue"><doi origin="wiley">10.1111/j.1439-0523.1997.tb02195.x</doi><idGroup><id type="unit" value="PBR589"></id></idGroup><countGroup><count type="pageTotal" number="3"></count></countGroup><titleGroup><title type="tocHeading1">Short Communication</title></titleGroup><eventGroup><event type="firstOnline" date="2006-04-28"></event><event type="publishedOnlineFinalForm" date="2006-04-28"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.5 mode:FullText source:HeaderRef result:HeaderRef" date="2010-04-07"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-06"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-11-03"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="589">589</numbering><numbering type="pageLast" number="591">591</numbering></numberingGroup><linkGroup><link type="toTypesetVersion" href="file:PBR.PBR589.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Received December 18, 1996/ Accepted August 13, 1997 Coiniminicated bv R. Koebner</unparsedEditorialHistory><countGroup><count type="referenceTotal" number="24"></count><count type="linksCrossRef" number="7"></count></countGroup><titleGroup><title type="main">Genetic diagnosis of Rehmannia species micropropagated by tip tissue culture and an F<sup>1</sup> hybrid by RAPD analysis</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>M.</givenNames><familyName>Hatano</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1"><personName><givenNames>R.</givenNames><familyName>Nakai</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a2"><personName><givenNames>F.</givenNames><familyName>Kawanishi2</familyName></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a2"><personName><givenNames>K.</givenNames><familyName>Kedo2</familyName></personName></creator><creator creatorRole="author" xml:id="cr5" affiliationRef="#a1"><personName><givenNames>Y.</givenNames><familyName>Shoyama1</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="JP"><unparsedAffiliation>Faculty of Pharmaceutical Sciences, Kyushu University, Higashiku, Fukuoka 812, Japan</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="JP"><unparsedAffiliation>Fukuchiyama Experitnental Farm, Takeda Chemical Industries Ltd, 4428‐2 Nagata, Fukuchiyama 620‐1, Japan</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1"><i>Rhemannia</i> spec.</keyword><keyword xml:id="k2">clonal micropropagation</keyword><keyword xml:id="k3">F<sub>1</sub> hybrid</keyword><keyword xml:id="k4">genetic homogeneity</keyword><keyword xml:id="k5">RAPD analysis</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Shoot formation was induced from the tip tissue of <i>Rehmannia glutinosa</i> f. <i>hueichingensis</i> on hormone‐free Murashige‐Skoog medium within 4 weeks of culture. Shoots were propagated on Murashige‐Skoog medium supplemented with l.0mg/l benzy0ladenine for 4 weeks. Propagated shoots rooted on the hormone‐free Murashige‐Skoog medium during 4 weeks of culture. Total DNA was extracted from the leaves of a F<sub>1</sub> hybrid and its parents. <i>R. glulinosa</i> f. <i>huekliingensis</i> and <i>R. glutinosa</i> var, <i>purpurea</i>. Analysis of random‐amplified polymorphic DNA (RAPD) using 10 arbitrary oligonucleotide 10‐mers. showed the genetic homogeneity ofthe above three species. The F<sub>1</sub> hybrid was genetically intermediate between both parental plants, compared with the genetic distance between the F<sub>1</sub> hybrid and individual parents. Furthermore, the comparison of the band patterns between the F<sub>1</sub> hybrid, obtained from the crossing clearly showed that parts of the bands of both parents. <i>R. glutinosa</i> f. <i>hueichingensis</i> and <i>R. glutinosa</i> var. <i>purpurea</i>, were introduced into the F<sub>1</sub> hybrid.</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="n-fnt-1" numbered="no"><p> <i>Wilh 2 figures</i> </p></note><note xml:id="n-fnt-2" numbered="no"><p> <i>Communicated by R. Koebner</i> </p></note></noteGroup></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Genetic diagnosis of Rehmannia species micropropagated by tip tissue culture and an F1 hybrid by RAPD analysis</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Genetic diagnosis of Rehmannia species micropropagated by tip tissue culture and an F1 hybrid by RAPD analysis</title></titleInfo><name type="personal"><namePart type="given">M.</namePart><namePart type="family">Hatano</namePart><affiliation>Faculty of Pharmaceutical Sciences, Kyushu University, Higashiku, Fukuoka 812, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">R.</namePart><namePart type="family">Nakai</namePart><affiliation>Faculty of Pharmaceutical Sciences, Kyushu University, Higashiku, Fukuoka 812, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">F.</namePart><namePart type="family">Kawanishi2</namePart><affiliation>Fukuchiyama Experitnental Farm, Takeda Chemical Industries Ltd, 4428‐2 Nagata, Fukuchiyama 620‐1, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K.</namePart><namePart type="family">Kedo2</namePart><affiliation>Fukuchiyama Experitnental Farm, Takeda Chemical Industries Ltd, 4428‐2 Nagata, Fukuchiyama 620‐1, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y.</namePart><namePart type="family">Shoyama1</namePart><affiliation>Faculty of Pharmaceutical Sciences, Kyushu University, Higashiku, Fukuoka 812, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">1997-12</dateIssued><edition>Received December 18, 1996/ Accepted August 13, 1997 Coiniminicated bv R. Koebner</edition><copyrightDate encoding="w3cdtf">1997</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="references">24</extent><extent unit="linksCrossRef">7</extent></physicalDescription><abstract lang="en">Shoot formation was induced from the tip tissue of Rehmannia glutinosa f. hueichingensis on hormone‐free Murashige‐Skoog medium within 4 weeks of culture. Shoots were propagated on Murashige‐Skoog medium supplemented with l.0mg/l benzy0ladenine for 4 weeks. Propagated shoots rooted on the hormone‐free Murashige‐Skoog medium during 4 weeks of culture. Total DNA was extracted from the leaves of a F1 hybrid and its parents. R. glulinosa f. huekliingensis and R. glutinosa var, purpurea. Analysis of random‐amplified polymorphic DNA (RAPD) using 10 arbitrary oligonucleotide 10‐mers. showed the genetic homogeneity ofthe above three species. The F1 hybrid was genetically intermediate between both parental plants, compared with the genetic distance between the F1 hybrid and individual parents. Furthermore, the comparison of the band patterns between the F1 hybrid, obtained from the crossing clearly showed that parts of the bands of both parents. R. glutinosa f. hueichingensis and R. glutinosa var. purpurea, were introduced into the F1 hybrid.</abstract><subject lang="en"><genre>keywords</genre><topic>Rhemannia spec.</topic><topic>clonal micropropagation</topic><topic>F1 hybrid</topic><topic>genetic homogeneity</topic><topic>RAPD analysis</topic></subject><relatedItem type="host"><titleInfo><title>Plant Breeding</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><identifier type="ISSN">0179-9541</identifier><identifier type="eISSN">1439-0523</identifier><identifier type="DOI">10.1111/(ISSN)1439-0523</identifier><identifier type="PublisherID">PBR</identifier><part><date>1997</date><detail type="volume"><caption>vol.</caption><number>116</number></detail><detail type="issue"><caption>no.</caption><number>6</number></detail><extent unit="pages"><start>589</start><end>591</end><total>3</total></extent></part></relatedItem><relatedItem type="references" displayLabel="cit1"><titleInfo><title>Comparison of chloroplast DNAs by specific fragmentation with EcoRI endonuclease</title></titleInfo><name type="personal"><namePart type="given">B. 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