ログイン
言語:

WEKO3

  • トップ
  • ランキング
To
lat lon distance
To

Field does not validate



インデックスリンク

インデックスツリー

メールアドレスを入力してください。

WEKO

One fine body…

WEKO

One fine body…

アイテム

  1. INDEX:組織別
  2. 農研機構 野菜花き研究部門
  3. 研究報告
  4. 花き研報
  5. 9号

カーネーションにおける DNA マーカーの育種への利用と品種多様性に関する研究

https://doi.org/10.24514/00001426
https://doi.org/10.24514/00001426
afe5dfe7-62d6-48a5-8f56-cbd5f8ddcef5
名前 / ファイル ライセンス アクション
frc_report_No9p53-89p.pdf frc_report_No9p53-89p.pdf (1.6 MB)
Item type 紀要論文01 / Departmental Bulletin Original Article(1)
公開日 2019-03-22
タイトル
タイトル カーネーションにおける DNA マーカーの育種への利用と品種多様性に関する研究
タイトル
タイトル Study on the Application of DNA Markers to Breeding and Identification of Cultivar Diversity in Carnation
言語 en
言語
言語 jpn
キーワード
主題Scheme Other
主題 Carnation
キーワード
主題Scheme Other
主題 Anthocyanin
キーワード
主題Scheme Other
主題 Bacterial wilt
キーワード
主題Scheme Other
主題 Flow cytometry (FCM)
キーワード
主題Scheme Other
主題 Polyploidy
キーワード
主題Scheme Other
主題 QTL
キーワード
主題Scheme Other
主題 RAPD
キーワード
主題Scheme Other
主題 SSR
キーワード
言語 en
主題Scheme Other
主題 Carnation
キーワード
言語 en
主題Scheme Other
主題 Anthocyanin
キーワード
言語 en
主題Scheme Other
主題 Bacterial wilt
キーワード
言語 en
主題Scheme Other
主題 Flow cytometry (FCM)
キーワード
言語 en
主題Scheme Other
主題 Polyploidy
キーワード
言語 en
主題Scheme Other
主題 QTL
キーワード
言語 en
主題Scheme Other
主題 RAPD
キーワード
言語 en
主題Scheme Other
主題 SSR
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ departmental bulletin paper
ID登録
ID登録 10.24514/00001426
ID登録タイプ JaLC
著者 八木, 雅史

× 八木, 雅史

八木, 雅史

ja-Kana ヤギ, マサフミ

en YAGI, Masafumi

Search repository
抄録
内容記述タイプ Abstract
内容記述 This study was carried out to utilize DNA markers in carnation (Dianthus caryophyllus L.) breeding and to clarify the genetic basis such as the ploidy level and genetic diversity of carnation cultivars. 1. Construction of genetic linkage map, quantitative trait locus (QTL) analysis and application to breeding in carnation To improve the selection efficiency in carnation breeding for resistance to bacterial wilt caused by Burkholderia caryophylli, the first genetic linkage map for the carnation was constructed by using a resistance-segregating population of 134 progeny lines derived from a cross between 'Carnation Nou No.1' (a line resistant to bacterial wilt) and 'Pretty Favvare' (a susceptible cultivar) based on RAPD and SSR analysis. The linkage map contained 137 RAPD and 9 SSR markers. Linkage analysis revealed that 124 loci could be mapped to 16 linkage groups that extended for 605.0 cM. The average interval between two loci was 4.9 cM. QTL analysis was applied to replication 8 evaluations of resistance to bacterial wilt. A QTL with a large resistance effect was detected on Group 6, which accounted for 60.5% of the total phenotypic variance with an LOD score of 23.46. Two other QTL with a small effect were detected on Groups 2 and 5 with LOD scores of 2.32 and 2.87, respectively. These results suggest that resistance to bacterial wilt in carnation is related to one major and at least two minor genes. The availability of marker-assisted selection (MAS) using DNA markers close to the QTL of resistance to bacterial wilt in carnation was examined. The STS-WG44 marker tightly linked to the major resistance gene was detected in all backcross lines with resistance selected by the root-soaking method. The ratio of markers OQ12 and STS-WB66 close to the two QTL with a small effect in resistant lines was lower in succeeding generations of backcrossing. These findings suggest that STS-WG44 is available for selecting resistant lines. In practical breeding populations, the difference in mean disease incidence between two groups categorized as having or lacking STS-WG44 was 62.6% and STS-WG44 was present in most lines showing disease incidence of less than 20%. These findings suggest that STS-WG44 as a selective marker facilitated the narrowing of populations to those that are highly resistant for practical breeding. MAS would be available for breeding improved resistance to bacterial wilt in carnation. Flower color is an important trait in ornamental plants. To understand the genetic basis for anthocyanin pigmentation traits in the flower petals of carnation, the segregation of anthocyanin content in petals was evaluated and QTL analysis was conducted by using the linkage map constructed in this study. The frequency of low anthocyanin content (<0.5 mg/g FW.) was highest and the frequency decreased in inverse proportion to anthocyanin content. QTL analysis identified two QTL on linkage Groups 6 and 9, which accounted for 21.6% and 15.0% of the total phenotypic variance, with LOD scores of 6.33 and 4.15, respectively. 2. Identification of ploidy level and cultivar diversity by flow cytometry (FCM) and SSR markers FCM was conducted to estimate the polyploidy level of 304 cut and 45 potted carnation cultivars preserved at the National Institute of Floricultural Science. To verify the actual level, the chromosome count in the root tips was investigated. In the cut carnation cultivars, an estimated 297 cultivars were diploid. Three cultivars ('Wiko', 'Scarlet Bell', and 'Spiral Vivid Red') were triploid and 'Saleya' was tetraploid. Another three cultivars ('Pink Roland', 'Youkihi', and 'Sonnet Sailor') were possibly tetraploid. In the 45 potted carnation cultivars, the results strongly suggested that 27 cultivars were diploid, three were triploid, and 15 were tetraploid. The chromosome count in the root tips revealed that 'Camille' was diploid, 'Baby Heart' was triploid, and 'Tula' was tetraploid. Our results suggest that the ploidy level varies among potted carnation cultivars. The stomatal length of 12 cut and 10 potted carnation cultivars was measured to determine if this method was convenient for distinguishing polyploidy. The results drew a distinction between diploid and polyploidy cultivars, but not between triploid and tetraploid. The genotypes of 32 cultivars were investigated by using five SSR markers to estimate the correspondence with the FCM ploidy levels and to analyze the genetic diversity. The ploidy estimated from the maximum number of alleles per locus corresponded with that estimated by FCM among the diploid and triploid cultivars, but not among the tetraploids. Among the diploid potted cultivars, only three or four alleles were found, and most of the alleles were also found in the diploid cut cultivars. On the other hand, triploid and tetraploid potted cultivars had four to eight alleles, and most were unique to a given ploidy levels. SSR analysis suggested that diploid potted cultivars were derived from cut cultivars because of their close genetic relationship, and that the triploids and tetraploids were produced by crossing wild Dianthus spp. and similar genetic resources because of their unique genetic background. In total, 30 potted cultivars with different ploidy levels could be successfully differentiated using five SSR markers.
書誌情報 花き研究所研究報告
en : Bulletin of the National Institute of Floricultural Science

巻 9, p. 53-89, 発行日 2009-12-20
出版者
出版者 独立行政法人 農業・食品産業技術総合研究機構 花き研究所
ISSN
収録物識別子タイプ ISSN
収録物識別子 1347-2917
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.24514/00001426
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
戻る
0
views
See details
Views

Versions

Ver.1 2023-05-15 15:49:53.132797
Show All versions

Share

Mendeley Twitter Facebook Print Addthis

Cite as

エクスポート

OAI-PMH
  • OAI-PMH JPCOAR 2.0
  • OAI-PMH JPCOAR 1.0
  • OAI-PMH DublinCore
  • OAI-PMH DDI
Other Formats
  • JSON
  • BIBTEX

Confirm


Powered by WEKO3


Powered by WEKO3