Segregation analysis of heading traits in hexaploid wheat utilizing recombinant inbred lines
The purpose of this study was to analyze the genetic segregation of heading traits in wheat using recombinant inbred lines (RILs) of hexaploid wheat, derived from Triticum aestivum cv. Chinese Spring and T. spelta var. duhameliamum . The population was examined under controlled environmental conditi...
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| description | The purpose of this study was to analyze the genetic segregation of heading traits in wheat using recombinant inbred lines (RILs) of hexaploid wheat, derived from
Triticum aestivum
cv. Chinese Spring and
T. spelta
var.
duhameliamum
. The population was examined under controlled environmental conditions as well as in the field. This strategy differentiated the effect of three genetic factors (vernalization requirement, photoperiod sensitivity and narrow-sense earliness) and identified their interactions. Correlation analysis showed that photoperiod sensitivity and narrow-sense earliness are critical for heading time in the field. Single-marker analysis using 322 molecular markers segregating among RIL detected a total of 38 linked markers for each genetic factor and heading in the field. In interval analysis, two
Vrn
genes (
Vrn-B1
and
Vrn-D1
) and
Ppd-B1
were mapped on chromosomes 5B, 5D and 2B, respectively. It was noticed that
Vrn-B1
on 5B from the spelt wheat conferred a strong-spring habit equivalent to the homoeologous
Vrn-A1
. Quantitative trait locus analysis also showed that
Ppd-B1
was not detected under the short-day condition without vernalization treatment, and that there were two types of genes for photoperiod sensitivity, dependent on and independent of vernalization treatment. |
| doi_str_mv | 10.1038/sj.hdy.6800178 |
| format | Article |
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Triticum aestivum
cv. Chinese Spring and
T. spelta
var.
duhameliamum
. The population was examined under controlled environmental conditions as well as in the field. This strategy differentiated the effect of three genetic factors (vernalization requirement, photoperiod sensitivity and narrow-sense earliness) and identified their interactions. Correlation analysis showed that photoperiod sensitivity and narrow-sense earliness are critical for heading time in the field. Single-marker analysis using 322 molecular markers segregating among RIL detected a total of 38 linked markers for each genetic factor and heading in the field. In interval analysis, two
Vrn
genes (
Vrn-B1
and
Vrn-D1
) and
Ppd-B1
were mapped on chromosomes 5B, 5D and 2B, respectively. It was noticed that
Vrn-B1
on 5B from the spelt wheat conferred a strong-spring habit equivalent to the homoeologous
Vrn-A1
. Quantitative trait locus analysis also showed that
Ppd-B1
was not detected under the short-day condition without vernalization treatment, and that there were two types of genes for photoperiod sensitivity, dependent on and independent of vernalization treatment.</description><identifier>ISSN: 0018-067X</identifier><identifier>EISSN: 1365-2540</identifier><identifier>DOI: 10.1038/sj.hdy.6800178</identifier><identifier>PMID: 12522426</identifier><identifier>CODEN: HDTYAT</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Chromosome Mapping ; Chromosomes ; Correlation analysis ; Cytogenetics ; Ecology ; Environmental conditions ; Evolutionary Biology ; Gene mapping ; gene segregation ; Genetic factors ; genetic markers ; heading ; heading date ; Human Genetics ; inbred lines ; narrow-sense earliness ; original-article ; Photoperiod ; photoperiod sensitivity ; photoperiodism ; Plant Genetics and Genomics ; Quantitative Trait Loci ; restriction fragment length polymorphism ; Time Factors ; Triticum - genetics ; Triticum - growth & development ; Triticum aestivum ; Triticum aestivum subsp. spelta ; vernalization requirement ; Wheat</subject><ispartof>Heredity, 2003-01, Vol.90 (1), p.56-63</ispartof><rights>The Genetics Society 2003</rights><rights>Copyright Nature Publishing Group Jan 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c541t-b42cf804719c117b294473467a9bc9682985d279a5d431893744a034165abb963</citedby><cites>FETCH-LOGICAL-c541t-b42cf804719c117b294473467a9bc9682985d279a5d431893744a034165abb963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2727,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12522426$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shindo, C</creatorcontrib><creatorcontrib>Tsujimoto, H</creatorcontrib><creatorcontrib>Sasakuma, T</creatorcontrib><title>Segregation analysis of heading traits in hexaploid wheat utilizing recombinant inbred lines</title><title>Heredity</title><addtitle>Heredity</addtitle><addtitle>Heredity (Edinb)</addtitle><description>The purpose of this study was to analyze the genetic segregation of heading traits in wheat using recombinant inbred lines (RILs) of hexaploid wheat, derived from
Triticum aestivum
cv. Chinese Spring and
T. spelta
var.
duhameliamum
. The population was examined under controlled environmental conditions as well as in the field. This strategy differentiated the effect of three genetic factors (vernalization requirement, photoperiod sensitivity and narrow-sense earliness) and identified their interactions. Correlation analysis showed that photoperiod sensitivity and narrow-sense earliness are critical for heading time in the field. Single-marker analysis using 322 molecular markers segregating among RIL detected a total of 38 linked markers for each genetic factor and heading in the field. In interval analysis, two
Vrn
genes (
Vrn-B1
and
Vrn-D1
) and
Ppd-B1
were mapped on chromosomes 5B, 5D and 2B, respectively. It was noticed that
Vrn-B1
on 5B from the spelt wheat conferred a strong-spring habit equivalent to the homoeologous
Vrn-A1
. Quantitative trait locus analysis also showed that
Ppd-B1
was not detected under the short-day condition without vernalization treatment, and that there were two types of genes for photoperiod sensitivity, dependent on and independent of vernalization treatment.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Chromosome Mapping</subject><subject>Chromosomes</subject><subject>Correlation analysis</subject><subject>Cytogenetics</subject><subject>Ecology</subject><subject>Environmental conditions</subject><subject>Evolutionary Biology</subject><subject>Gene mapping</subject><subject>gene segregation</subject><subject>Genetic factors</subject><subject>genetic markers</subject><subject>heading</subject><subject>heading date</subject><subject>Human Genetics</subject><subject>inbred lines</subject><subject>narrow-sense earliness</subject><subject>original-article</subject><subject>Photoperiod</subject><subject>photoperiod sensitivity</subject><subject>photoperiodism</subject><subject>Plant Genetics and Genomics</subject><subject>Quantitative Trait Loci</subject><subject>restriction fragment length polymorphism</subject><subject>Time Factors</subject><subject>Triticum - genetics</subject><subject>Triticum - growth & development</subject><subject>Triticum aestivum</subject><subject>Triticum aestivum subsp. spelta</subject><subject>vernalization requirement</subject><subject>Wheat</subject><issn>0018-067X</issn><issn>1365-2540</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkc1rFEEQxRsxmDV69aYOOXibTX9NfxwlGBUCHmLAg9D0zPRMepntXrt60PWvT4dZXAgETwX1fvWKqofQG4LXBDN1AZv1Xb9fC4UxkeoZWhEmmpo2HD9Hq9JTNRbyxyl6CbDBGDNJ9Qt0SmhDKadihX7euDG50WYfQ2WDnfbgoYpDdeds78NY5WR9hsqH0vljd1P0ffW7iLmas5_83wcmuS5uWx9syAVsk-uryQcHr9DJYCdwrw_1DN1effp--aW-_vb56-XH67prOMl1y2k3KMwl0R0hsqWac8m4kFa3nRaKatX0VGrb9JwRpZnk3GLGiWhs22rBztCHxXeX4q_ZQTZbD52bJhtcnMGUowWjqvkvSJTQinNewPNH4CbOqbwHDGXlj1QQVqD1AnUpAiQ3mF3yW5v2hmDzkI6BjSnpmEM6ZeDdwXVut64_4oc4CnCxAFCkMLp0XPuk5dtlItg8J_fP8qi_X_TBRmPH5MHc3lBMGCaYMqUJuwe0A604</recordid><startdate>20030101</startdate><enddate>20030101</enddate><creator>Shindo, C</creator><creator>Tsujimoto, H</creator><creator>Sasakuma, T</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>FBQ</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>3V.</scope><scope>7QL</scope><scope>7SN</scope><scope>7SS</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20030101</creationdate><title>Segregation analysis of heading traits in hexaploid wheat utilizing recombinant inbred lines</title><author>Shindo, C ; Tsujimoto, H ; Sasakuma, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c541t-b42cf804719c117b294473467a9bc9682985d279a5d431893744a034165abb963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Chromosome Mapping</topic><topic>Chromosomes</topic><topic>Correlation analysis</topic><topic>Cytogenetics</topic><topic>Ecology</topic><topic>Environmental conditions</topic><topic>Evolutionary Biology</topic><topic>Gene mapping</topic><topic>gene segregation</topic><topic>Genetic factors</topic><topic>genetic markers</topic><topic>heading</topic><topic>heading date</topic><topic>Human Genetics</topic><topic>inbred lines</topic><topic>narrow-sense earliness</topic><topic>original-article</topic><topic>Photoperiod</topic><topic>photoperiod sensitivity</topic><topic>photoperiodism</topic><topic>Plant Genetics and Genomics</topic><topic>Quantitative Trait Loci</topic><topic>restriction fragment length polymorphism</topic><topic>Time Factors</topic><topic>Triticum - genetics</topic><topic>Triticum - growth & development</topic><topic>Triticum aestivum</topic><topic>Triticum aestivum subsp. spelta</topic><topic>vernalization requirement</topic><topic>Wheat</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shindo, C</creatorcontrib><creatorcontrib>Tsujimoto, H</creatorcontrib><creatorcontrib>Sasakuma, T</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Research Library</collection><collection>ProQuest Science Journals</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Heredity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shindo, C</au><au>Tsujimoto, H</au><au>Sasakuma, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Segregation analysis of heading traits in hexaploid wheat utilizing recombinant inbred lines</atitle><jtitle>Heredity</jtitle><stitle>Heredity</stitle><addtitle>Heredity (Edinb)</addtitle><date>2003-01-01</date><risdate>2003</risdate><volume>90</volume><issue>1</issue><spage>56</spage><epage>63</epage><pages>56-63</pages><issn>0018-067X</issn><eissn>1365-2540</eissn><coden>HDTYAT</coden><abstract>The purpose of this study was to analyze the genetic segregation of heading traits in wheat using recombinant inbred lines (RILs) of hexaploid wheat, derived from
Triticum aestivum
cv. Chinese Spring and
T. spelta
var.
duhameliamum
. The population was examined under controlled environmental conditions as well as in the field. This strategy differentiated the effect of three genetic factors (vernalization requirement, photoperiod sensitivity and narrow-sense earliness) and identified their interactions. Correlation analysis showed that photoperiod sensitivity and narrow-sense earliness are critical for heading time in the field. Single-marker analysis using 322 molecular markers segregating among RIL detected a total of 38 linked markers for each genetic factor and heading in the field. In interval analysis, two
Vrn
genes (
Vrn-B1
and
Vrn-D1
) and
Ppd-B1
were mapped on chromosomes 5B, 5D and 2B, respectively. It was noticed that
Vrn-B1
on 5B from the spelt wheat conferred a strong-spring habit equivalent to the homoeologous
Vrn-A1
. Quantitative trait locus analysis also showed that
Ppd-B1
was not detected under the short-day condition without vernalization treatment, and that there were two types of genes for photoperiod sensitivity, dependent on and independent of vernalization treatment.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>12522426</pmid><doi>10.1038/sj.hdy.6800178</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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| ispartof | Heredity, 2003-01, Vol.90 (1), p.56-63 |
| issn | 0018-067X 1365-2540 |
| language | eng |
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| source | MEDLINE; Nature; Alma/SFX Local Collection; EZB Electronic Journals Library |
| subjects | Biomedical and Life Sciences Biomedicine Chromosome Mapping Chromosomes Correlation analysis Cytogenetics Ecology Environmental conditions Evolutionary Biology Gene mapping gene segregation Genetic factors genetic markers heading heading date Human Genetics inbred lines narrow-sense earliness original-article Photoperiod photoperiod sensitivity photoperiodism Plant Genetics and Genomics Quantitative Trait Loci restriction fragment length polymorphism Time Factors Triticum - genetics Triticum - growth & development Triticum aestivum Triticum aestivum subsp. spelta vernalization requirement Wheat |
| title | Segregation analysis of heading traits in hexaploid wheat utilizing recombinant inbred lines |
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