SSR markers developed using next-generation sequencing technology in pineapple, Ananas comosus (L.) Merr

  • Nashima Kenji
    College of Bioresource Sciences, Nihon University
  • Hosaka Fumiko
    Institute of Fruit Tree and Tea Science, National Agriculture and Food Research Organization
  • Terakami Shingo
    Institute of Fruit Tree and Tea Science, National Agriculture and Food Research Organization
  • Kunihisa Miyuki
    Institute of Fruit Tree and Tea Science, National Agriculture and Food Research Organization
  • Nishitani Chikako
    Institute of Fruit Tree and Tea Science, National Agriculture and Food Research Organization
  • Moromizato Chie
    Okinawa Prefectural Agricultural Research Center Nago Branch
  • Takeuchi Makoto
    Okinawa Prefectural Agricultural Research Center Nago Branch
  • Shoda Moriyuki
    Okinawa Prefectural Agricultural Research Center
  • Tarora Kazuhiko
    Okinawa Prefectural Agricultural Research Center
  • Urasaki Naoya
    Okinawa Prefectural Agricultural Research Center
  • Yamamoto Toshiya
    Institute of Fruit Tree and Tea Science, National Agriculture and Food Research Organization

書誌事項

タイトル別名
  • SSR markers developed using next-generation sequencing technology in pineapple, <i>Ananas comosus</i> (L.) Merr.

この論文をさがす

抄録

<p>Simple sequence repeat (SSR) markers provide a reliable tool for the identification of accessions and the construction of genetic linkage maps because of their co-dominant inheritance. In the present study, we developed new SSR markers with next-generation sequencing using the Roche 454 GS FLX+ platform. Five hundred SSR primer sets were tested for the genetic identification of pineapple, including 100 each for the di-, tri-, tetra-, penta-, and hexa-nucleotide motif SSRs. In total, 160 SSR markers successfully amplified fragments and exhibited polymorphism among accessions. The SSR markers revealed the number of alleles per locus (ranging from 2 to 13), the expected heterozygosity (ranging from 0.041 to 0.823), and the observed heterozygosity (ranging from 0 to 0.875). A total of 117 SSR markers with tri- or greater nucleotide motifs were shown to be effective at facilitating accurate genotyping. Using the SSR markers, 25 accessions were distinguished genetically, with the exception of accessions ‘MD-2’ and ‘Yonekura’. The developed SSR markers could facilitate the establishment of efficient and accurate genetic identification systems and the construction of genetic linkage maps in the future.</p>

収録刊行物

被引用文献 (1)*注記

もっと見る

参考文献 (20)*注記

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ