Mapping of the male sterile mutant gene ftms in Brassica rapa L. ssp. pekinensis via BSR-Seq combined with whole-genome resequencing
Key message A male sterile mutant was created by 60 Co γ-rays of microspores isolated from Chinese cabbage DH line ‘FT’. A candidate gene for the male sterile trait was identified as Bra010198 . Male sterility is used for hybrid seed production in Chinese cabbage. In this study, we derived a male st...
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creator | Tan, Chong Liu, Zhiyong Huang, Shengnan Feng, Hui |
description | Key message
A male sterile mutant was created by
60
Co γ-rays of microspores isolated from Chinese cabbage DH line ‘FT’. A candidate gene for the male sterile trait was identified as
Bra010198
.
Male sterility is used for hybrid seed production in Chinese cabbage. In this study, we derived a male sterile mutant (
ftms
) from Chinese cabbage DH line ‘FT’ by irradiating microspores with
60
Co γ-rays and realized the rapid trait transformation from male fertility to sterility for creating valuable breeding materials. Genetic analysis indicated that the male sterile trait is controlled by a single recessive nuclear gene,
ftms
. Microspore development in mutant
ftms
was aborted at the tetrad stage and associated with severely retarded degeneration and vacuolation of tapetum. Using BSR-seq analysis, the candidate region for
ftms
was mapped on chromosome A05. A large
F
2
population was created, and the region was narrowed to approximately 1.7-Mb between markers Indel20 and Indel14 via linkage analysis. The recombination frequency was extremely suppressed because the region was located on the chromosome A05 centromere. Whole-genome resequencing of mutant
ftms
and wild-type ‘FT’ aligned only one nonsynonymous SNP to
Bra010198
; this gene is a homolog of
Arabidopsis KNS4/UPEX1,
which encodes a putative
β
-(1,3)-galactosyltransferase that controls pollen exine development. Comparative sequencing verified the SNP position on the fifth exon of
Bra010198
in mutant
ftms
. Further genotyping revealed that the male sterile phenotype was fully co-segregated with this SNP. Quantitative real-time PCR indicated that
Bra0101918
specifically expressed in stamen. The data presented herein suggested that
Bra010198
is a strong candidate gene for
ftms
. Hence, we developed a male sterile line for potential application in breeding and expanded the knowledge about the molecular mechanism underlying male sterility in Chinese cabbage. |
doi_str_mv | 10.1007/s00122-018-3223-2 |
format | Article |
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A male sterile mutant was created by
60
Co γ-rays of microspores isolated from Chinese cabbage DH line ‘FT’. A candidate gene for the male sterile trait was identified as
Bra010198
.
Male sterility is used for hybrid seed production in Chinese cabbage. In this study, we derived a male sterile mutant (
ftms
) from Chinese cabbage DH line ‘FT’ by irradiating microspores with
60
Co γ-rays and realized the rapid trait transformation from male fertility to sterility for creating valuable breeding materials. Genetic analysis indicated that the male sterile trait is controlled by a single recessive nuclear gene,
ftms
. Microspore development in mutant
ftms
was aborted at the tetrad stage and associated with severely retarded degeneration and vacuolation of tapetum. Using BSR-seq analysis, the candidate region for
ftms
was mapped on chromosome A05. A large
F
2
population was created, and the region was narrowed to approximately 1.7-Mb between markers Indel20 and Indel14 via linkage analysis. The recombination frequency was extremely suppressed because the region was located on the chromosome A05 centromere. Whole-genome resequencing of mutant
ftms
and wild-type ‘FT’ aligned only one nonsynonymous SNP to
Bra010198
; this gene is a homolog of
Arabidopsis KNS4/UPEX1,
which encodes a putative
β
-(1,3)-galactosyltransferase that controls pollen exine development. Comparative sequencing verified the SNP position on the fifth exon of
Bra010198
in mutant
ftms
. Further genotyping revealed that the male sterile phenotype was fully co-segregated with this SNP. Quantitative real-time PCR indicated that
Bra0101918
specifically expressed in stamen. The data presented herein suggested that
Bra010198
is a strong candidate gene for
ftms
. Hence, we developed a male sterile line for potential application in breeding and expanded the knowledge about the molecular mechanism underlying male sterility in Chinese cabbage.</description><identifier>ISSN: 0040-5752</identifier><identifier>EISSN: 1432-2242</identifier><identifier>DOI: 10.1007/s00122-018-3223-2</identifier><identifier>PMID: 30382313</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Agriculture ; Amino Acid Sequence ; Arabidopsis ; Arabidopsis thaliana ; Base Sequence ; Biochemistry ; Biomedical and Life Sciences ; Biotechnology ; Brassica ; Brassica oleracea ; Brassica rapa - genetics ; Breeding ; Chromosome Mapping ; Chromosomes ; Data processing ; Degeneration ; Gene mapping ; Gene mutation ; Genes ; Genes, Plant ; Genes, Recessive ; Genetic analysis ; Genetic aspects ; Genetic transformation ; Genomes ; Genomics ; Genotyping ; Identification and classification ; Life Sciences ; Linkage analysis ; Male sterility ; Original Article ; Phenotypes ; Plant Biochemistry ; Plant Breeding ; Plant Breeding/Biotechnology ; Plant Genetics and Genomics ; Plant Infertility - genetics ; Plant sterility ; Recombination ; Seed industry ; Seeds ; Single nucleotide polymorphisms ; Single-nucleotide polymorphism</subject><ispartof>Theoretical and applied genetics, 2019-02, Vol.132 (2), p.355-370</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2018</rights><rights>COPYRIGHT 2019 Springer</rights><rights>Theoretical and Applied Genetics is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-8aac0b57f94aff2e37496ca2a0ac9ac53dde8daf5b895dc26c43f6cfe83610763</citedby><cites>FETCH-LOGICAL-c473t-8aac0b57f94aff2e37496ca2a0ac9ac53dde8daf5b895dc26c43f6cfe83610763</cites><orcidid>0000-0002-6345-6633</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00122-018-3223-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00122-018-3223-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30382313$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tan, Chong</creatorcontrib><creatorcontrib>Liu, Zhiyong</creatorcontrib><creatorcontrib>Huang, Shengnan</creatorcontrib><creatorcontrib>Feng, Hui</creatorcontrib><title>Mapping of the male sterile mutant gene ftms in Brassica rapa L. ssp. pekinensis via BSR-Seq combined with whole-genome resequencing</title><title>Theoretical and applied genetics</title><addtitle>Theor Appl Genet</addtitle><addtitle>Theor Appl Genet</addtitle><description>Key message
A male sterile mutant was created by
60
Co γ-rays of microspores isolated from Chinese cabbage DH line ‘FT’. A candidate gene for the male sterile trait was identified as
Bra010198
.
Male sterility is used for hybrid seed production in Chinese cabbage. In this study, we derived a male sterile mutant (
ftms
) from Chinese cabbage DH line ‘FT’ by irradiating microspores with
60
Co γ-rays and realized the rapid trait transformation from male fertility to sterility for creating valuable breeding materials. Genetic analysis indicated that the male sterile trait is controlled by a single recessive nuclear gene,
ftms
. Microspore development in mutant
ftms
was aborted at the tetrad stage and associated with severely retarded degeneration and vacuolation of tapetum. Using BSR-seq analysis, the candidate region for
ftms
was mapped on chromosome A05. A large
F
2
population was created, and the region was narrowed to approximately 1.7-Mb between markers Indel20 and Indel14 via linkage analysis. The recombination frequency was extremely suppressed because the region was located on the chromosome A05 centromere. Whole-genome resequencing of mutant
ftms
and wild-type ‘FT’ aligned only one nonsynonymous SNP to
Bra010198
; this gene is a homolog of
Arabidopsis KNS4/UPEX1,
which encodes a putative
β
-(1,3)-galactosyltransferase that controls pollen exine development. Comparative sequencing verified the SNP position on the fifth exon of
Bra010198
in mutant
ftms
. Further genotyping revealed that the male sterile phenotype was fully co-segregated with this SNP. Quantitative real-time PCR indicated that
Bra0101918
specifically expressed in stamen. The data presented herein suggested that
Bra010198
is a strong candidate gene for
ftms
. Hence, we developed a male sterile line for potential application in breeding and expanded the knowledge about the molecular mechanism underlying male sterility in Chinese cabbage.</description><subject>Agriculture</subject><subject>Amino Acid Sequence</subject><subject>Arabidopsis</subject><subject>Arabidopsis thaliana</subject><subject>Base Sequence</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Brassica</subject><subject>Brassica oleracea</subject><subject>Brassica rapa - genetics</subject><subject>Breeding</subject><subject>Chromosome Mapping</subject><subject>Chromosomes</subject><subject>Data processing</subject><subject>Degeneration</subject><subject>Gene mapping</subject><subject>Gene mutation</subject><subject>Genes</subject><subject>Genes, Plant</subject><subject>Genes, Recessive</subject><subject>Genetic analysis</subject><subject>Genetic aspects</subject><subject>Genetic transformation</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Genotyping</subject><subject>Identification and classification</subject><subject>Life Sciences</subject><subject>Linkage analysis</subject><subject>Male sterility</subject><subject>Original Article</subject><subject>Phenotypes</subject><subject>Plant Biochemistry</subject><subject>Plant Breeding</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Infertility - genetics</subject><subject>Plant sterility</subject><subject>Recombination</subject><subject>Seed industry</subject><subject>Seeds</subject><subject>Single nucleotide polymorphisms</subject><subject>Single-nucleotide polymorphism</subject><issn>0040-5752</issn><issn>1432-2242</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kk9v1DAQxSMEokvhA3BBlri0hyz-EyfOsa0oVFqE1IWz5XXGuy4bJ_U4FO58cLxsoVoE8mEk-_feeEavKF4yOmeUNm-QUsZ5SZkqBeei5I-KGasELzmv-ONiRmlFS9lIflQ8Q7yhlHJJxdPiSFChuGBiVvz4YMbRhzUZHEkbIL3ZAsEE0efaT8mERNYQgLjUI_GBnEeD6K0h0YyGLOYEcZyTEb74AAE9kq_ekPPldbmEW2KHfpXvO3Ln04bcbYYtlNlt6IFEQLidINjc_HnxxJktwov7elx8vnz76eJ9ufj47uribFHaqhGpVMZYupKNayvjHAfRVG1tDTfU2NZYKboOVGecXKlWdpbXthKutg6UqBltanFcnOx9xzjk3ph079HCdmsCDBNqznjTVq1SVUZf_4XeDFMM-Xe_KKmUbOsHap3Xpn1wQ4rG7kz1mWyYrBSvd9T8H1Q-HfTeDgFcXvah4PRAkJkE39LaTIj6anl9yLI9a-OAGMHpMfrexO-aUb1Lid6nROeU6F1KNM-aV_fDTaseuj-K37HIAN8DmJ_CGuLD9P93_QnG-MWX</recordid><startdate>20190201</startdate><enddate>20190201</enddate><creator>Tan, Chong</creator><creator>Liu, Zhiyong</creator><creator>Huang, Shengnan</creator><creator>Feng, Hui</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>7X8</scope><orcidid>https://orcid.org/0000-0002-6345-6633</orcidid></search><sort><creationdate>20190201</creationdate><title>Mapping of the male sterile mutant gene ftms in Brassica rapa L. ssp. pekinensis via BSR-Seq combined with whole-genome resequencing</title><author>Tan, Chong ; Liu, Zhiyong ; Huang, Shengnan ; Feng, Hui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c473t-8aac0b57f94aff2e37496ca2a0ac9ac53dde8daf5b895dc26c43f6cfe83610763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Agriculture</topic><topic>Amino Acid Sequence</topic><topic>Arabidopsis</topic><topic>Arabidopsis thaliana</topic><topic>Base Sequence</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Brassica</topic><topic>Brassica oleracea</topic><topic>Brassica rapa - genetics</topic><topic>Breeding</topic><topic>Chromosome Mapping</topic><topic>Chromosomes</topic><topic>Data processing</topic><topic>Degeneration</topic><topic>Gene mapping</topic><topic>Gene mutation</topic><topic>Genes</topic><topic>Genes, Plant</topic><topic>Genes, Recessive</topic><topic>Genetic analysis</topic><topic>Genetic aspects</topic><topic>Genetic transformation</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Genotyping</topic><topic>Identification and classification</topic><topic>Life Sciences</topic><topic>Linkage analysis</topic><topic>Male sterility</topic><topic>Original Article</topic><topic>Phenotypes</topic><topic>Plant Biochemistry</topic><topic>Plant Breeding</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Infertility - genetics</topic><topic>Plant sterility</topic><topic>Recombination</topic><topic>Seed industry</topic><topic>Seeds</topic><topic>Single nucleotide polymorphisms</topic><topic>Single-nucleotide polymorphism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tan, Chong</creatorcontrib><creatorcontrib>Liu, Zhiyong</creatorcontrib><creatorcontrib>Huang, Shengnan</creatorcontrib><creatorcontrib>Feng, Hui</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>MEDLINE - Academic</collection><jtitle>Theoretical and applied genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tan, Chong</au><au>Liu, Zhiyong</au><au>Huang, Shengnan</au><au>Feng, Hui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mapping of the male sterile mutant gene ftms in Brassica rapa L. ssp. pekinensis via BSR-Seq combined with whole-genome resequencing</atitle><jtitle>Theoretical and applied genetics</jtitle><stitle>Theor Appl Genet</stitle><addtitle>Theor Appl Genet</addtitle><date>2019-02-01</date><risdate>2019</risdate><volume>132</volume><issue>2</issue><spage>355</spage><epage>370</epage><pages>355-370</pages><issn>0040-5752</issn><eissn>1432-2242</eissn><abstract>Key message
A male sterile mutant was created by
60
Co γ-rays of microspores isolated from Chinese cabbage DH line ‘FT’. A candidate gene for the male sterile trait was identified as
Bra010198
.
Male sterility is used for hybrid seed production in Chinese cabbage. In this study, we derived a male sterile mutant (
ftms
) from Chinese cabbage DH line ‘FT’ by irradiating microspores with
60
Co γ-rays and realized the rapid trait transformation from male fertility to sterility for creating valuable breeding materials. Genetic analysis indicated that the male sterile trait is controlled by a single recessive nuclear gene,
ftms
. Microspore development in mutant
ftms
was aborted at the tetrad stage and associated with severely retarded degeneration and vacuolation of tapetum. Using BSR-seq analysis, the candidate region for
ftms
was mapped on chromosome A05. A large
F
2
population was created, and the region was narrowed to approximately 1.7-Mb between markers Indel20 and Indel14 via linkage analysis. The recombination frequency was extremely suppressed because the region was located on the chromosome A05 centromere. Whole-genome resequencing of mutant
ftms
and wild-type ‘FT’ aligned only one nonsynonymous SNP to
Bra010198
; this gene is a homolog of
Arabidopsis KNS4/UPEX1,
which encodes a putative
β
-(1,3)-galactosyltransferase that controls pollen exine development. Comparative sequencing verified the SNP position on the fifth exon of
Bra010198
in mutant
ftms
. Further genotyping revealed that the male sterile phenotype was fully co-segregated with this SNP. Quantitative real-time PCR indicated that
Bra0101918
specifically expressed in stamen. The data presented herein suggested that
Bra010198
is a strong candidate gene for
ftms
. Hence, we developed a male sterile line for potential application in breeding and expanded the knowledge about the molecular mechanism underlying male sterility in Chinese cabbage.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>30382313</pmid><doi>10.1007/s00122-018-3223-2</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-6345-6633</orcidid></addata></record> |
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language | eng |
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source | MEDLINE; SpringerNature Journals |
subjects | Agriculture Amino Acid Sequence Arabidopsis Arabidopsis thaliana Base Sequence Biochemistry Biomedical and Life Sciences Biotechnology Brassica Brassica oleracea Brassica rapa - genetics Breeding Chromosome Mapping Chromosomes Data processing Degeneration Gene mapping Gene mutation Genes Genes, Plant Genes, Recessive Genetic analysis Genetic aspects Genetic transformation Genomes Genomics Genotyping Identification and classification Life Sciences Linkage analysis Male sterility Original Article Phenotypes Plant Biochemistry Plant Breeding Plant Breeding/Biotechnology Plant Genetics and Genomics Plant Infertility - genetics Plant sterility Recombination Seed industry Seeds Single nucleotide polymorphisms Single-nucleotide polymorphism |
title | Mapping of the male sterile mutant gene ftms in Brassica rapa L. ssp. pekinensis via BSR-Seq combined with whole-genome resequencing |
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