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

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+ plat...

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Autores principales: Nashima, Kenji, Hosaka, Fumiko, Terakami, Shingo, Kunihisa, Miyuki, Nishitani, Chikako, Moromizato, Chie, Takeuchi, Makoto, Shoda, Moriyuki, Tarora, Kazuhiko, Urasaki, Naoya, Yamamoto, Toshiya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society of Breeding 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372017/
https://www.ncbi.nlm.nih.gov/pubmed/32714066
http://dx.doi.org/10.1270/jsbbs.19158
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author Nashima, Kenji
Hosaka, Fumiko
Terakami, Shingo
Kunihisa, Miyuki
Nishitani, Chikako
Moromizato, Chie
Takeuchi, Makoto
Shoda, Moriyuki
Tarora, Kazuhiko
Urasaki, Naoya
Yamamoto, Toshiya
author_facet Nashima, Kenji
Hosaka, Fumiko
Terakami, Shingo
Kunihisa, Miyuki
Nishitani, Chikako
Moromizato, Chie
Takeuchi, Makoto
Shoda, Moriyuki
Tarora, Kazuhiko
Urasaki, Naoya
Yamamoto, Toshiya
author_sort Nashima, Kenji
collection PubMed
description 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.
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spelling pubmed-73720172020-07-23 SSR markers developed using next-generation sequencing technology in pineapple, Ananas comosus (L.) Merr. Nashima, Kenji Hosaka, Fumiko Terakami, Shingo Kunihisa, Miyuki Nishitani, Chikako Moromizato, Chie Takeuchi, Makoto Shoda, Moriyuki Tarora, Kazuhiko Urasaki, Naoya Yamamoto, Toshiya Breed Sci Note 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. Japanese Society of Breeding 2020-06 2020-05-30 /pmc/articles/PMC7372017/ /pubmed/32714066 http://dx.doi.org/10.1270/jsbbs.19158 Text en Copyright © 2020 by JAPANESE SOCIETY OF BREEDING http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Note
Nashima, Kenji
Hosaka, Fumiko
Terakami, Shingo
Kunihisa, Miyuki
Nishitani, Chikako
Moromizato, Chie
Takeuchi, Makoto
Shoda, Moriyuki
Tarora, Kazuhiko
Urasaki, Naoya
Yamamoto, Toshiya
SSR markers developed using next-generation sequencing technology in pineapple, Ananas comosus (L.) Merr.
title SSR markers developed using next-generation sequencing technology in pineapple, Ananas comosus (L.) Merr.
title_full SSR markers developed using next-generation sequencing technology in pineapple, Ananas comosus (L.) Merr.
title_fullStr SSR markers developed using next-generation sequencing technology in pineapple, Ananas comosus (L.) Merr.
title_full_unstemmed SSR markers developed using next-generation sequencing technology in pineapple, Ananas comosus (L.) Merr.
title_short SSR markers developed using next-generation sequencing technology in pineapple, Ananas comosus (L.) Merr.
title_sort ssr markers developed using next-generation sequencing technology in pineapple, ananas comosus (l.) merr.
topic Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372017/
https://www.ncbi.nlm.nih.gov/pubmed/32714066
http://dx.doi.org/10.1270/jsbbs.19158
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