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Exploration and Exploitation of Novel SSR Markers for Candidate Transcription Factor Genes in Lilium Species
Lilies (Lilium sp.) are commercially important horticultural crops widely cultivated for their flowers and bulbs. Here, we conducted large-scale data mining of the lily transcriptome to develop transcription factor (TF)-associated microsatellite markers (TFSSRs). Among 216,768 unigenes extracted fro...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852593/ https://www.ncbi.nlm.nih.gov/pubmed/29443955 http://dx.doi.org/10.3390/genes9020097 |
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author | Biswas, Manosh Kumar Nath, Ujjal Kumar Howlader, Jewel Bagchi, Mita Natarajan, Sathishkumar Kayum, Md Abdul Kim, Hoy-Taek Park, Jong-In Kang, Jong-Goo Nou, Ill-Sup |
author_facet | Biswas, Manosh Kumar Nath, Ujjal Kumar Howlader, Jewel Bagchi, Mita Natarajan, Sathishkumar Kayum, Md Abdul Kim, Hoy-Taek Park, Jong-In Kang, Jong-Goo Nou, Ill-Sup |
author_sort | Biswas, Manosh Kumar |
collection | PubMed |
description | Lilies (Lilium sp.) are commercially important horticultural crops widely cultivated for their flowers and bulbs. Here, we conducted large-scale data mining of the lily transcriptome to develop transcription factor (TF)-associated microsatellite markers (TFSSRs). Among 216,768 unigenes extracted from our sequence data, 6966 unigenes harbored simple sequence repeats (SSRs). Seventy-one SSRs were associated with TF genes, and these were used to design primers and validate their potential as markers. These 71 SSRs were accomplished with 31 transcription factor families; including bHLH, MYB, C2H2, ERF, C3H, NAC, bZIP, and so on. Fourteen highly polymorphic SSRs were selected based on Polymorphic Information Content (PIC) values and used to study genetic diversity and population structure in lily accessions. Higher genetic diversity was observed in Longiflorum compared to Oriental and Asiatic populations. Lily accessions were divided into three sub-populations based in our structure analysis, and an un-rooted neighbor-joining tree effectively separated the accessions according to Asiatic, Oriental, and Longiflorum subgroups. Finally, we showed that 46 of the SSR-associated genes were differentially expressed in response to Botrytis elliptica infection. Thus, our newly developed TFSSR markers represent a powerful tool for large-scale genotyping, high-density and comparative mapping, marker-aided backcrossing, and molecular diversity analysis of Lilium sp. |
format | Online Article Text |
id | pubmed-5852593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58525932018-03-19 Exploration and Exploitation of Novel SSR Markers for Candidate Transcription Factor Genes in Lilium Species Biswas, Manosh Kumar Nath, Ujjal Kumar Howlader, Jewel Bagchi, Mita Natarajan, Sathishkumar Kayum, Md Abdul Kim, Hoy-Taek Park, Jong-In Kang, Jong-Goo Nou, Ill-Sup Genes (Basel) Article Lilies (Lilium sp.) are commercially important horticultural crops widely cultivated for their flowers and bulbs. Here, we conducted large-scale data mining of the lily transcriptome to develop transcription factor (TF)-associated microsatellite markers (TFSSRs). Among 216,768 unigenes extracted from our sequence data, 6966 unigenes harbored simple sequence repeats (SSRs). Seventy-one SSRs were associated with TF genes, and these were used to design primers and validate their potential as markers. These 71 SSRs were accomplished with 31 transcription factor families; including bHLH, MYB, C2H2, ERF, C3H, NAC, bZIP, and so on. Fourteen highly polymorphic SSRs were selected based on Polymorphic Information Content (PIC) values and used to study genetic diversity and population structure in lily accessions. Higher genetic diversity was observed in Longiflorum compared to Oriental and Asiatic populations. Lily accessions were divided into three sub-populations based in our structure analysis, and an un-rooted neighbor-joining tree effectively separated the accessions according to Asiatic, Oriental, and Longiflorum subgroups. Finally, we showed that 46 of the SSR-associated genes were differentially expressed in response to Botrytis elliptica infection. Thus, our newly developed TFSSR markers represent a powerful tool for large-scale genotyping, high-density and comparative mapping, marker-aided backcrossing, and molecular diversity analysis of Lilium sp. MDPI 2018-02-14 /pmc/articles/PMC5852593/ /pubmed/29443955 http://dx.doi.org/10.3390/genes9020097 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Biswas, Manosh Kumar Nath, Ujjal Kumar Howlader, Jewel Bagchi, Mita Natarajan, Sathishkumar Kayum, Md Abdul Kim, Hoy-Taek Park, Jong-In Kang, Jong-Goo Nou, Ill-Sup Exploration and Exploitation of Novel SSR Markers for Candidate Transcription Factor Genes in Lilium Species |
title | Exploration and Exploitation of Novel SSR Markers for Candidate Transcription Factor Genes in Lilium Species |
title_full | Exploration and Exploitation of Novel SSR Markers for Candidate Transcription Factor Genes in Lilium Species |
title_fullStr | Exploration and Exploitation of Novel SSR Markers for Candidate Transcription Factor Genes in Lilium Species |
title_full_unstemmed | Exploration and Exploitation of Novel SSR Markers for Candidate Transcription Factor Genes in Lilium Species |
title_short | Exploration and Exploitation of Novel SSR Markers for Candidate Transcription Factor Genes in Lilium Species |
title_sort | exploration and exploitation of novel ssr markers for candidate transcription factor genes in lilium species |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852593/ https://www.ncbi.nlm.nih.gov/pubmed/29443955 http://dx.doi.org/10.3390/genes9020097 |
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