Development of EST-SSR markers of Ipomoea nil
Although Japanese morning glory (Ipomoea nil (L.) Roth.) has been used intensively for genetic studies, DNA markers have not been developed in Ipomoea nil sufficient to cover all chromosomes. Therefore, we conducted microsatellite (simple sequence repeats, SSR) marker development in I. nil for futur...
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Japanese Society of Breeding
2012
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405949/ |
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pubmed-34059492012-11-07 Development of EST-SSR markers of Ipomoea nil Ly, Tong Fukuoka, Hiroyuki Otaka, Asami Hoshino, Atsushi Iida, Shigeru Nitasaka, Eiji Watanabe, Nobuyoshi Kuboyama, Tsutomu Note Although Japanese morning glory (Ipomoea nil (L.) Roth.) has been used intensively for genetic studies, DNA markers have not been developed in Ipomoea nil sufficient to cover all chromosomes. Therefore, we conducted microsatellite (simple sequence repeats, SSR) marker development in I. nil for future genetic studies. From 92,662 expressed sequence tag (EST) sequences, 514 unique microsatellite-containing ESTs were identified. Primer pairs were designed automatically in 326 SSRs. Of 150 SSRs examined, 75 showed polymorphisms among strains. A phenogram based on the SSR genotypes revealed the genetic relation among seven Japanese morning glories from five different regions of the world and an ivyleaf morning glory (I. hederacea Jacq.). The developed SSR markers might be applicable for genetic studies of morning glories and their relatives. Japanese Society of Breeding 2012-03-20 2012-03 /pmc/articles/PMC3405949/ /pubmed/23136520 http://dx.doi.org/10.1270/jsbbs.62.99 Text en Copyright © 2012 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. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Ly, Tong Fukuoka, Hiroyuki Otaka, Asami Hoshino, Atsushi Iida, Shigeru Nitasaka, Eiji Watanabe, Nobuyoshi Kuboyama, Tsutomu |
spellingShingle |
Ly, Tong Fukuoka, Hiroyuki Otaka, Asami Hoshino, Atsushi Iida, Shigeru Nitasaka, Eiji Watanabe, Nobuyoshi Kuboyama, Tsutomu Development of EST-SSR markers of Ipomoea nil |
author_facet |
Ly, Tong Fukuoka, Hiroyuki Otaka, Asami Hoshino, Atsushi Iida, Shigeru Nitasaka, Eiji Watanabe, Nobuyoshi Kuboyama, Tsutomu |
author_sort |
Ly, Tong |
title |
Development of EST-SSR markers of Ipomoea nil |
title_short |
Development of EST-SSR markers of Ipomoea nil |
title_full |
Development of EST-SSR markers of Ipomoea nil |
title_fullStr |
Development of EST-SSR markers of Ipomoea nil |
title_full_unstemmed |
Development of EST-SSR markers of Ipomoea nil |
title_sort |
development of est-ssr markers of ipomoea nil |
description |
Although Japanese morning glory (Ipomoea nil (L.) Roth.) has been used intensively for genetic studies, DNA markers have not been developed in Ipomoea nil sufficient to cover all chromosomes. Therefore, we conducted microsatellite (simple sequence repeats, SSR) marker development in I. nil for future genetic studies. From 92,662 expressed sequence tag (EST) sequences, 514 unique microsatellite-containing ESTs were identified. Primer pairs were designed automatically in 326 SSRs. Of 150 SSRs examined, 75 showed polymorphisms among strains. A phenogram based on the SSR genotypes revealed the genetic relation among seven Japanese morning glories from five different regions of the world and an ivyleaf morning glory (I. hederacea Jacq.). The developed SSR markers might be applicable for genetic studies of morning glories and their relatives. |
publisher |
Japanese Society of Breeding |
publishDate |
2012 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405949/ |
_version_ |
1611545787866546176 |