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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Veröffentlicht in:Theoretical and applied genetics 2019-02, Vol.132 (2), p.355-370
Hauptverfasser: Tan, Chong, Liu, Zhiyong, Huang, Shengnan, Feng, Hui
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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.
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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 . 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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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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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