Dissection of gene loci underlying pasting temperature in cassava
© 2018 Informa UK Limited, trading as Taylor & Francis Group. In this study, a fine genetic map within the quantitative trait loci (QTL) underlying pasting temperature (PT) of cassava (Manihot esculenta Crantz) was constructed using newly developed simple sequence repeat (SSR) markers. The SSR...
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th-mahidol.447162019-08-23T17:30:46Z Dissection of gene loci underlying pasting temperature in cassava Nattaya Srisawad Wikanda Worrapitirungsi Supajit Sraphet Opas Boonseng Duncan R. Smith Kanokporn Triwitayakorn Thailand Ministry of Agriculture and Cooperatives Mahidol University Center of Excellence on Agricultural Biotechnology: (AG-BIO/PERDO-CHE) Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology © 2018 Informa UK Limited, trading as Taylor & Francis Group. In this study, a fine genetic map within the quantitative trait loci (QTL) underlying pasting temperature (PT) of cassava (Manihot esculenta Crantz) was constructed using newly developed simple sequence repeat (SSR) markers. The SSRs were designed on the basis of two scaffolds (S11341 and S4043) of the cassava genome, which covered previously identified QTL regions of the PT trait. A total of 55 and 61 SSR markers derived from S11341 and S4043, respectively, representing 0.29% of the cassava genome, were generated; of which 23 and 19 showed informative polymorphic patterns. Consequently, all identified informative polymorphic markers were used to genotype 200 F1 progeny plants. The genotypic data were then analyzed, and the results showed that 480 markers were distributed across 23 linkage groups (LGs) with total length of 1,334 centimorgans (cM). An analysis of QTL underlying the PT trait revealed that marker EME81 on LG 1 had significant associations (P < 0.0001) in all environments evaluated. Four candidate genes were identified and selected for gene expression analysis in the parents, and among F1 lines with high and low PT values. Significant differences were observed in relative expression of carbohydrate phosphorylase (CP) and starch synthase II (SSII) between high and low PT in 6-month-old cassava. We found CP and SSII genes to potentially control the PT trait. In addition, the marker EME81 was found to be a promising marker for specific PT trait selection in cassava populations, which should facilitate marker-assisted selection for desired PT traits. 2019-08-23T10:15:49Z 2019-08-23T10:15:49Z 2018-07-04 Article Journal of Crop Improvement. Vol.32, No.4 (2018), 493-510 10.1080/15427528.2018.1458364 15427536 15427528 2-s2.0-85045028520 https://repository.li.mahidol.ac.th/handle/123456789/44716 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85045028520&origin=inward |
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Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology Nattaya Srisawad Wikanda Worrapitirungsi Supajit Sraphet Opas Boonseng Duncan R. Smith Kanokporn Triwitayakorn Dissection of gene loci underlying pasting temperature in cassava |
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© 2018 Informa UK Limited, trading as Taylor & Francis Group. In this study, a fine genetic map within the quantitative trait loci (QTL) underlying pasting temperature (PT) of cassava (Manihot esculenta Crantz) was constructed using newly developed simple sequence repeat (SSR) markers. The SSRs were designed on the basis of two scaffolds (S11341 and S4043) of the cassava genome, which covered previously identified QTL regions of the PT trait. A total of 55 and 61 SSR markers derived from S11341 and S4043, respectively, representing 0.29% of the cassava genome, were generated; of which 23 and 19 showed informative polymorphic patterns. Consequently, all identified informative polymorphic markers were used to genotype 200 F1 progeny plants. The genotypic data were then analyzed, and the results showed that 480 markers were distributed across 23 linkage groups (LGs) with total length of 1,334 centimorgans (cM). An analysis of QTL underlying the PT trait revealed that marker EME81 on LG 1 had significant associations (P < 0.0001) in all environments evaluated. Four candidate genes were identified and selected for gene expression analysis in the parents, and among F1 lines with high and low PT values. Significant differences were observed in relative expression of carbohydrate phosphorylase (CP) and starch synthase II (SSII) between high and low PT in 6-month-old cassava. We found CP and SSII genes to potentially control the PT trait. In addition, the marker EME81 was found to be a promising marker for specific PT trait selection in cassava populations, which should facilitate marker-assisted selection for desired PT traits. |
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Thailand Ministry of Agriculture and Cooperatives |
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Thailand Ministry of Agriculture and Cooperatives Nattaya Srisawad Wikanda Worrapitirungsi Supajit Sraphet Opas Boonseng Duncan R. Smith Kanokporn Triwitayakorn |
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Article |
author |
Nattaya Srisawad Wikanda Worrapitirungsi Supajit Sraphet Opas Boonseng Duncan R. Smith Kanokporn Triwitayakorn |
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Nattaya Srisawad |
title |
Dissection of gene loci underlying pasting temperature in cassava |
title_short |
Dissection of gene loci underlying pasting temperature in cassava |
title_full |
Dissection of gene loci underlying pasting temperature in cassava |
title_fullStr |
Dissection of gene loci underlying pasting temperature in cassava |
title_full_unstemmed |
Dissection of gene loci underlying pasting temperature in cassava |
title_sort |
dissection of gene loci underlying pasting temperature in cassava |
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2019 |
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https://repository.li.mahidol.ac.th/handle/123456789/44716 |
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1763498192697032704 |