Construction of a high-density linkage map and mapping quantitative trait loci for somatic embryogenesis using leaf petioles as explants in upland cotton (Gossypium hirsutum L.)

Key message The first high-density linkage map was constructed to identify quantitative trait loci (QTLs) for somatic embryogenesis (SE) in cotton ( Gossypium hirsutum L.) using leaf petioles as explants. Cotton transformation is highly limited by only a few regenerable genotypes and the lack of und...

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Veröffentlicht in:Plant cell reports 2015-07, Vol.34 (7), p.1177-1187
Hauptverfasser: Xu, Zhenzhen, Zhang, Chaojun, Ge, Xiaoyang, Wang, Ni, Zhou, Kehai, Yang, Xiaojie, Wu, Zhixia, Zhang, Xueyan, Liu, Chuanliang, Yang, Zuoren, Li, Changfeng, Liu, Kun, Yang, Zhaoen, Qian, Yuyuan, Li, Fuguang
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container_end_page 1187
container_issue 7
container_start_page 1177
container_title Plant cell reports
container_volume 34
creator Xu, Zhenzhen
Zhang, Chaojun
Ge, Xiaoyang
Wang, Ni
Zhou, Kehai
Yang, Xiaojie
Wu, Zhixia
Zhang, Xueyan
Liu, Chuanliang
Yang, Zuoren
Li, Changfeng
Liu, Kun
Yang, Zhaoen
Qian, Yuyuan
Li, Fuguang
description Key message The first high-density linkage map was constructed to identify quantitative trait loci (QTLs) for somatic embryogenesis (SE) in cotton ( Gossypium hirsutum L.) using leaf petioles as explants. Cotton transformation is highly limited by only a few regenerable genotypes and the lack of understanding of the genetic and molecular basis of somatic embryogenesis (SE) in cotton ( Gossypium hirsutum L.). To construct a more saturated linkage map and further identify quantitative trait loci (QTLs) for SE using leaf petioles as explants, a high embryogenesis frequency line (W10) from the commercial Chinese cotton cultivar CRI24 was crossed with TM-1, a genetic standard upland cotton with no embryogenesis frequency. The genetic map spanned 2300.41 cM in genetic distance and contained 411 polymorphic simple sequence repeat (SSR) loci. Of the 411 mapped loci, 25 were developed from unigenes identified for SE in our previous study. Six QTLs for SE were detected by composite interval mapping method, each explaining 6.88–37.07 % of the phenotypic variance. Single marker analysis was also performed to verify the reliability of QTLs detection, and the SSR markers NAU3325 and DPL0209 were detected by the two methods. Further studies on the relatively stable and anchoring QTLs/markers for SE in an advanced population of W10 × TM-1 and other cross combinations with different SE abilities may shed light on the genetic and molecular mechanism of SE in cotton.
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Cotton transformation is highly limited by only a few regenerable genotypes and the lack of understanding of the genetic and molecular basis of somatic embryogenesis (SE) in cotton ( Gossypium hirsutum L.). To construct a more saturated linkage map and further identify quantitative trait loci (QTLs) for SE using leaf petioles as explants, a high embryogenesis frequency line (W10) from the commercial Chinese cotton cultivar CRI24 was crossed with TM-1, a genetic standard upland cotton with no embryogenesis frequency. The genetic map spanned 2300.41 cM in genetic distance and contained 411 polymorphic simple sequence repeat (SSR) loci. Of the 411 mapped loci, 25 were developed from unigenes identified for SE in our previous study. Six QTLs for SE were detected by composite interval mapping method, each explaining 6.88–37.07 % of the phenotypic variance. Single marker analysis was also performed to verify the reliability of QTLs detection, and the SSR markers NAU3325 and DPL0209 were detected by the two methods. 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Cotton transformation is highly limited by only a few regenerable genotypes and the lack of understanding of the genetic and molecular basis of somatic embryogenesis (SE) in cotton ( Gossypium hirsutum L.). To construct a more saturated linkage map and further identify quantitative trait loci (QTLs) for SE using leaf petioles as explants, a high embryogenesis frequency line (W10) from the commercial Chinese cotton cultivar CRI24 was crossed with TM-1, a genetic standard upland cotton with no embryogenesis frequency. The genetic map spanned 2300.41 cM in genetic distance and contained 411 polymorphic simple sequence repeat (SSR) loci. Of the 411 mapped loci, 25 were developed from unigenes identified for SE in our previous study. Six QTLs for SE were detected by composite interval mapping method, each explaining 6.88–37.07 % of the phenotypic variance. Single marker analysis was also performed to verify the reliability of QTLs detection, and the SSR markers NAU3325 and DPL0209 were detected by the two methods. 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Zhang, Chaojun ; Ge, Xiaoyang ; Wang, Ni ; Zhou, Kehai ; Yang, Xiaojie ; Wu, Zhixia ; Zhang, Xueyan ; Liu, Chuanliang ; Yang, Zuoren ; Li, Changfeng ; Liu, Kun ; Yang, Zhaoen ; Qian, Yuyuan ; Li, Fuguang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-12da8879d9e3c9242ac6626c2b3a967da5bc828f325f082062396c682e0719d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Base Sequence</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Cell Biology</topic><topic>Chromosome Mapping - methods</topic><topic>Chromosome Segregation - genetics</topic><topic>Cotton</topic><topic>Crosses, Genetic</topic><topic>Cultivars</topic><topic>Embryonic growth stage</topic><topic>Expressed Sequence Tags</topic><topic>Gene mapping</topic><topic>Genetic Linkage</topic><topic>Genetic Markers</topic><topic>Genotypes</topic><topic>Gossypium - embryology</topic><topic>Gossypium - genetics</topic><topic>Gossypium hirsutum</topic><topic>Life Sciences</topic><topic>Microsatellite Repeats - genetics</topic><topic>Original Paper</topic><topic>Plant Biochemistry</topic><topic>Plant Leaves - genetics</topic><topic>Plant Sciences</topic><topic>Plant Somatic Embryogenesis Techniques</topic><topic>Quantitative Trait Loci - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Zhenzhen</creatorcontrib><creatorcontrib>Zhang, Chaojun</creatorcontrib><creatorcontrib>Ge, Xiaoyang</creatorcontrib><creatorcontrib>Wang, Ni</creatorcontrib><creatorcontrib>Zhou, Kehai</creatorcontrib><creatorcontrib>Yang, Xiaojie</creatorcontrib><creatorcontrib>Wu, Zhixia</creatorcontrib><creatorcontrib>Zhang, Xueyan</creatorcontrib><creatorcontrib>Liu, Chuanliang</creatorcontrib><creatorcontrib>Yang, Zuoren</creatorcontrib><creatorcontrib>Li, Changfeng</creatorcontrib><creatorcontrib>Liu, Kun</creatorcontrib><creatorcontrib>Yang, Zhaoen</creatorcontrib><creatorcontrib>Qian, Yuyuan</creatorcontrib><creatorcontrib>Li, Fuguang</creatorcontrib><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>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; 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Cotton transformation is highly limited by only a few regenerable genotypes and the lack of understanding of the genetic and molecular basis of somatic embryogenesis (SE) in cotton ( Gossypium hirsutum L.). To construct a more saturated linkage map and further identify quantitative trait loci (QTLs) for SE using leaf petioles as explants, a high embryogenesis frequency line (W10) from the commercial Chinese cotton cultivar CRI24 was crossed with TM-1, a genetic standard upland cotton with no embryogenesis frequency. The genetic map spanned 2300.41 cM in genetic distance and contained 411 polymorphic simple sequence repeat (SSR) loci. Of the 411 mapped loci, 25 were developed from unigenes identified for SE in our previous study. Six QTLs for SE were detected by composite interval mapping method, each explaining 6.88–37.07 % of the phenotypic variance. Single marker analysis was also performed to verify the reliability of QTLs detection, and the SSR markers NAU3325 and DPL0209 were detected by the two methods. Further studies on the relatively stable and anchoring QTLs/markers for SE in an advanced population of W10 × TM-1 and other cross combinations with different SE abilities may shed light on the genetic and molecular mechanism of SE in cotton.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>25758337</pmid><doi>10.1007/s00299-015-1776-y</doi><tpages>11</tpages></addata></record>
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subjects Base Sequence
Biomedical and Life Sciences
Biotechnology
Cell Biology
Chromosome Mapping - methods
Chromosome Segregation - genetics
Cotton
Crosses, Genetic
Cultivars
Embryonic growth stage
Expressed Sequence Tags
Gene mapping
Genetic Linkage
Genetic Markers
Genotypes
Gossypium - embryology
Gossypium - genetics
Gossypium hirsutum
Life Sciences
Microsatellite Repeats - genetics
Original Paper
Plant Biochemistry
Plant Leaves - genetics
Plant Sciences
Plant Somatic Embryogenesis Techniques
Quantitative Trait Loci - genetics
title Construction of a high-density linkage map and mapping quantitative trait loci for somatic embryogenesis using leaf petioles as explants in upland cotton (Gossypium hirsutum L.)
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