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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Veröffentlicht in:Theoretical and applied genetics 2018, Vol.131 (1), p.13-25
Hauptverfasser: Wang, Kunyang, Lin, Zhishan, Wang, Long, Wang, Ke, Shi, Qinghua, Du, Lipu, Ye, Xingguo
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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
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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. 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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 ; 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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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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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