Development of a set of PCR markers specific to Aegilops longissima chromosome arms and application in breeding a translocation line
Key message Transcriptome data were used to develop 134 Aegilops longissima specific PCR markers and their comparative maps were constructed by contrasting with the homologous genes in the wheat B genome. Three wheat– Ae. longissima 1BL·1S l S translocation lines were identified using the correspond...
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creator | Wang, Kunyang Lin, Zhishan Wang, Long Wang, Ke Shi, Qinghua Du, Lipu Ye, Xingguo |
description | Key message
Transcriptome data were used to develop 134
Aegilops longissima
specific PCR markers and their comparative maps were constructed by contrasting with the homologous genes in the wheat B genome. Three wheat–
Ae. longissima
1BL·1S
l
S translocation lines were identified using the correspondence markers.
Aegilops longissima
is an important wild species of common wheat that harbors many genes that can be used to improve various traits of common wheat (
Triticum aestivum
L.). To efficiently transfer the traits conferred by these
Ae. longissima
genes into wheat, we sequenced the whole expression transcript of
Ae. longissima
. Using the transcriptome data, we developed 134 specific polymerase chain reaction markers located on the 14 chromosome arms of
Ae. longissima
. These novel molecular markers were assigned to specific chromosome locations based on a comparison with the homologous genes in the B genome of wheat. Annotation of these genes showed that most had functions related to metabolic processes, hydrolase activity, or catalytic activity. Additionally, we used these markers to identify three wheat–
Ae. longissima
1BL·1S
l
S translocation lines in somatic variation populations resulting from a cross between wheat cultivar Westonia and a wheat–
Ae. longissima
substitution line 1S
l
(1B). The translocation lines had several low molecular weight glutenin subunits encoding genes beneficial to flour processing quality that came from
Ae. longissima
1S
l
S. The three translocation lines were also confirmed by genomic in situ hybridization. These translocation lines will be further evaluated for potential quality improvement of bread-making properties of wheat. |
doi_str_mv | 10.1007/s00122-017-2982-5 |
format | Article |
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Transcriptome data were used to develop 134
Aegilops longissima
specific PCR markers and their comparative maps were constructed by contrasting with the homologous genes in the wheat B genome. Three wheat–
Ae. longissima
1BL·1S
l
S translocation lines were identified using the correspondence markers.
Aegilops longissima
is an important wild species of common wheat that harbors many genes that can be used to improve various traits of common wheat (
Triticum aestivum
L.). To efficiently transfer the traits conferred by these
Ae. longissima
genes into wheat, we sequenced the whole expression transcript of
Ae. longissima
. Using the transcriptome data, we developed 134 specific polymerase chain reaction markers located on the 14 chromosome arms of
Ae. longissima
. These novel molecular markers were assigned to specific chromosome locations based on a comparison with the homologous genes in the B genome of wheat. Annotation of these genes showed that most had functions related to metabolic processes, hydrolase activity, or catalytic activity. Additionally, we used these markers to identify three wheat–
Ae. longissima
1BL·1S
l
S translocation lines in somatic variation populations resulting from a cross between wheat cultivar Westonia and a wheat–
Ae. longissima
substitution line 1S
l
(1B). The translocation lines had several low molecular weight glutenin subunits encoding genes beneficial to flour processing quality that came from
Ae. longissima
1S
l
S. The three translocation lines were also confirmed by genomic in situ hybridization. These translocation lines will be further evaluated for potential quality improvement of bread-making properties of wheat.</description><identifier>ISSN: 0040-5752</identifier><identifier>EISSN: 1432-2242</identifier><identifier>DOI: 10.1007/s00122-017-2982-5</identifier><identifier>PMID: 28887628</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Aegilops longissima ; Agriculture ; Biochemistry ; Biomedical and Life Sciences ; Biotechnology ; breadmaking ; Breeding ; Catalytic activity ; Chromosomes ; Chromosomes, Plant ; clonal variation ; cultivars ; Data processing ; enzyme activity ; flour ; Gene expression ; Gene loci ; Gene mapping ; genes ; Genetic aspects ; Genetic Markers ; Genomes ; Genomic in situ hybridization ; genomics ; Glutenin ; glutenins ; Glutens ; Goat grass ; Grasses ; Homology ; Hydrolase ; in situ hybridization ; Life Sciences ; Low molecular weights ; Molecular weight ; Observations ; Original Article ; Plant Biochemistry ; Plant Breeding ; Plant Breeding/Biotechnology ; Plant Genetics and Genomics ; Poaceae - genetics ; Polymerase Chain Reaction ; processing quality ; Quality control ; substitution lines ; Substitution reactions ; Transcription ; Transcriptome ; Translocation ; translocation lines ; Translocation, Genetic ; Translocations (Genetics) ; Triticum ; Triticum aestivum ; Wheat</subject><ispartof>Theoretical and applied genetics, 2018, Vol.131 (1), p.13-25</ispartof><rights>Springer-Verlag GmbH Germany 2017</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Theoretical and Applied Genetics is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-b93c9201266e4cd801e205835a84dc2d64262bbe2de85b40e86ea3316d11c5053</citedby><cites>FETCH-LOGICAL-c506t-b93c9201266e4cd801e205835a84dc2d64262bbe2de85b40e86ea3316d11c5053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00122-017-2982-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00122-017-2982-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28887628$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Kunyang</creatorcontrib><creatorcontrib>Lin, Zhishan</creatorcontrib><creatorcontrib>Wang, Long</creatorcontrib><creatorcontrib>Wang, Ke</creatorcontrib><creatorcontrib>Shi, Qinghua</creatorcontrib><creatorcontrib>Du, Lipu</creatorcontrib><creatorcontrib>Ye, Xingguo</creatorcontrib><title>Development of a set of PCR markers specific to Aegilops longissima chromosome arms and application in breeding a translocation line</title><title>Theoretical and applied genetics</title><addtitle>Theor Appl Genet</addtitle><addtitle>Theor Appl Genet</addtitle><description>Key message
Transcriptome data were used to develop 134
Aegilops longissima
specific PCR markers and their comparative maps were constructed by contrasting with the homologous genes in the wheat B genome. Three wheat–
Ae. longissima
1BL·1S
l
S translocation lines were identified using the correspondence markers.
Aegilops longissima
is an important wild species of common wheat that harbors many genes that can be used to improve various traits of common wheat (
Triticum aestivum
L.). To efficiently transfer the traits conferred by these
Ae. longissima
genes into wheat, we sequenced the whole expression transcript of
Ae. longissima
. Using the transcriptome data, we developed 134 specific polymerase chain reaction markers located on the 14 chromosome arms of
Ae. longissima
. These novel molecular markers were assigned to specific chromosome locations based on a comparison with the homologous genes in the B genome of wheat. Annotation of these genes showed that most had functions related to metabolic processes, hydrolase activity, or catalytic activity. Additionally, we used these markers to identify three wheat–
Ae. longissima
1BL·1S
l
S translocation lines in somatic variation populations resulting from a cross between wheat cultivar Westonia and a wheat–
Ae. longissima
substitution line 1S
l
(1B). The translocation lines had several low molecular weight glutenin subunits encoding genes beneficial to flour processing quality that came from
Ae. longissima
1S
l
S. The three translocation lines were also confirmed by genomic in situ hybridization. These translocation lines will be further evaluated for potential quality improvement of bread-making properties of wheat.</description><subject>Aegilops longissima</subject><subject>Agriculture</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>breadmaking</subject><subject>Breeding</subject><subject>Catalytic activity</subject><subject>Chromosomes</subject><subject>Chromosomes, Plant</subject><subject>clonal variation</subject><subject>cultivars</subject><subject>Data processing</subject><subject>enzyme activity</subject><subject>flour</subject><subject>Gene expression</subject><subject>Gene loci</subject><subject>Gene mapping</subject><subject>genes</subject><subject>Genetic aspects</subject><subject>Genetic Markers</subject><subject>Genomes</subject><subject>Genomic in situ hybridization</subject><subject>genomics</subject><subject>Glutenin</subject><subject>glutenins</subject><subject>Glutens</subject><subject>Goat grass</subject><subject>Grasses</subject><subject>Homology</subject><subject>Hydrolase</subject><subject>in situ hybridization</subject><subject>Life Sciences</subject><subject>Low molecular weights</subject><subject>Molecular weight</subject><subject>Observations</subject><subject>Original Article</subject><subject>Plant Biochemistry</subject><subject>Plant Breeding</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Genetics and Genomics</subject><subject>Poaceae - genetics</subject><subject>Polymerase Chain Reaction</subject><subject>processing quality</subject><subject>Quality control</subject><subject>substitution lines</subject><subject>Substitution reactions</subject><subject>Transcription</subject><subject>Transcriptome</subject><subject>Translocation</subject><subject>translocation lines</subject><subject>Translocation, Genetic</subject><subject>Translocations (Genetics)</subject><subject>Triticum</subject><subject>Triticum aestivum</subject><subject>Wheat</subject><issn>0040-5752</issn><issn>1432-2242</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kktv1DAUhSMEokPhB7BBltjAIsW-jh3PcjTlUakSqMDacpyb4JLYwU4Q3feH42GGxyCQF7Z8v3t8j3yK4jGjZ4zS-kWilAGUlNUlrBWU4k6xYhWHEqCCu8WK0oqWohZwUjxI6ZpSCoLy-8UJKKVqCWpV3J7jVxzCNKKfSeiIIQl_HN5tr8ho4meMiaQJreucJXMgG-xd5hMZgu9dSm40xH6KYQwpjEhMHBMxviVmmgZnzeyCJ86TJiK2zvf5gTkan4ZwqA3O48PiXmeGhI8O-2nx8dXLD9s35eXb1xfbzWVpBZVz2ay5XUO2LCVWtlWUIVChuDCqai20sgIJTYPQohJNRVFJNJwz2TKWFQQ_LZ7tdacYviyYZj26ZHEYjMewJA2MSbWuOJcZffoXeh2W6PN0mq0VlwA1F7-p3gyone9CNmd3onojgAGtZa0ydfYPKq8WR2eDx87l-6OG50cNmZnx29ybJSV98f7qmGV71saQUsROTzH_SbzRjOpdSvQ-JTqnRO9SondjPzmYW5oR218dP2ORAdgDKZd8j_EP9_9V_Q5bqcUK</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Wang, Kunyang</creator><creator>Lin, Zhishan</creator><creator>Wang, Long</creator><creator>Wang, Ke</creator><creator>Shi, Qinghua</creator><creator>Du, Lipu</creator><creator>Ye, Xingguo</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><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>ISR</scope><scope>3V.</scope><scope>7SS</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>2018</creationdate><title>Development of a set of PCR markers specific to Aegilops longissima chromosome arms and application in breeding a translocation line</title><author>Wang, Kunyang ; Lin, Zhishan ; Wang, Long ; Wang, Ke ; Shi, Qinghua ; Du, Lipu ; Ye, Xingguo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-b93c9201266e4cd801e205835a84dc2d64262bbe2de85b40e86ea3316d11c5053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aegilops longissima</topic><topic>Agriculture</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>breadmaking</topic><topic>Breeding</topic><topic>Catalytic activity</topic><topic>Chromosomes</topic><topic>Chromosomes, Plant</topic><topic>clonal variation</topic><topic>cultivars</topic><topic>Data processing</topic><topic>enzyme activity</topic><topic>flour</topic><topic>Gene expression</topic><topic>Gene loci</topic><topic>Gene mapping</topic><topic>genes</topic><topic>Genetic aspects</topic><topic>Genetic Markers</topic><topic>Genomes</topic><topic>Genomic in situ hybridization</topic><topic>genomics</topic><topic>Glutenin</topic><topic>glutenins</topic><topic>Glutens</topic><topic>Goat grass</topic><topic>Grasses</topic><topic>Homology</topic><topic>Hydrolase</topic><topic>in situ hybridization</topic><topic>Life Sciences</topic><topic>Low molecular weights</topic><topic>Molecular weight</topic><topic>Observations</topic><topic>Original Article</topic><topic>Plant Biochemistry</topic><topic>Plant Breeding</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant Genetics and Genomics</topic><topic>Poaceae - genetics</topic><topic>Polymerase Chain Reaction</topic><topic>processing quality</topic><topic>Quality control</topic><topic>substitution lines</topic><topic>Substitution reactions</topic><topic>Transcription</topic><topic>Transcriptome</topic><topic>Translocation</topic><topic>translocation lines</topic><topic>Translocation, Genetic</topic><topic>Translocations (Genetics)</topic><topic>Triticum</topic><topic>Triticum aestivum</topic><topic>Wheat</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Kunyang</creatorcontrib><creatorcontrib>Lin, Zhishan</creatorcontrib><creatorcontrib>Wang, Long</creatorcontrib><creatorcontrib>Wang, Ke</creatorcontrib><creatorcontrib>Shi, Qinghua</creatorcontrib><creatorcontrib>Du, Lipu</creatorcontrib><creatorcontrib>Ye, Xingguo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>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>Medical Database</collection><collection>Biological Science Database</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 China</collection><collection>Genetics Abstracts</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Theoretical and applied genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Kunyang</au><au>Lin, Zhishan</au><au>Wang, Long</au><au>Wang, Ke</au><au>Shi, Qinghua</au><au>Du, Lipu</au><au>Ye, Xingguo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a set of PCR markers specific to Aegilops longissima chromosome arms and application in breeding a translocation line</atitle><jtitle>Theoretical and applied genetics</jtitle><stitle>Theor Appl Genet</stitle><addtitle>Theor Appl Genet</addtitle><date>2018</date><risdate>2018</risdate><volume>131</volume><issue>1</issue><spage>13</spage><epage>25</epage><pages>13-25</pages><issn>0040-5752</issn><eissn>1432-2242</eissn><abstract>Key message
Transcriptome data were used to develop 134
Aegilops longissima
specific PCR markers and their comparative maps were constructed by contrasting with the homologous genes in the wheat B genome. Three wheat–
Ae. longissima
1BL·1S
l
S translocation lines were identified using the correspondence markers.
Aegilops longissima
is an important wild species of common wheat that harbors many genes that can be used to improve various traits of common wheat (
Triticum aestivum
L.). To efficiently transfer the traits conferred by these
Ae. longissima
genes into wheat, we sequenced the whole expression transcript of
Ae. longissima
. Using the transcriptome data, we developed 134 specific polymerase chain reaction markers located on the 14 chromosome arms of
Ae. longissima
. These novel molecular markers were assigned to specific chromosome locations based on a comparison with the homologous genes in the B genome of wheat. Annotation of these genes showed that most had functions related to metabolic processes, hydrolase activity, or catalytic activity. Additionally, we used these markers to identify three wheat–
Ae. longissima
1BL·1S
l
S translocation lines in somatic variation populations resulting from a cross between wheat cultivar Westonia and a wheat–
Ae. longissima
substitution line 1S
l
(1B). The translocation lines had several low molecular weight glutenin subunits encoding genes beneficial to flour processing quality that came from
Ae. longissima
1S
l
S. The three translocation lines were also confirmed by genomic in situ hybridization. These translocation lines will be further evaluated for potential quality improvement of bread-making properties of wheat.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28887628</pmid><doi>10.1007/s00122-017-2982-5</doi><tpages>13</tpages></addata></record> |
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language | eng |
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source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Aegilops longissima Agriculture Biochemistry Biomedical and Life Sciences Biotechnology breadmaking Breeding Catalytic activity Chromosomes Chromosomes, Plant clonal variation cultivars Data processing enzyme activity flour Gene expression Gene loci Gene mapping genes Genetic aspects Genetic Markers Genomes Genomic in situ hybridization genomics Glutenin glutenins Glutens Goat grass Grasses Homology Hydrolase in situ hybridization Life Sciences Low molecular weights Molecular weight Observations Original Article Plant Biochemistry Plant Breeding Plant Breeding/Biotechnology Plant Genetics and Genomics Poaceae - genetics Polymerase Chain Reaction processing quality Quality control substitution lines Substitution reactions Transcription Transcriptome Translocation translocation lines Translocation, Genetic Translocations (Genetics) Triticum Triticum aestivum Wheat |
title | Development of a set of PCR markers specific to Aegilops longissima chromosome arms and application in breeding a translocation line |
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