Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers

Clonal reproduction of oil palm by means of tissue culture is a very inefficient process. Tissue culturability is known to be genotype dependent with some genotypes being more amenable to tissue culture than others. In this study, genetic linkage maps enriched with simple sequence repeat (SSR) marke...

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Main Authors: Ting, Ngoot Chin, Jansen, Johannes, Nagappan, Jayanthi, Ishak, Zamzuri, Chin, Cheuk Weng, Tan, Soon Guan, Cheah, Suan Choo, Singh, Rajinder
Format: Article
Language:English
Published: Public Library of Science 2013
Online Access:http://psasir.upm.edu.my/id/eprint/28028/
http://psasir.upm.edu.my/id/eprint/28028/1/journal.pone.0053076.pdf
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author Ting, Ngoot Chin
Jansen, Johannes
Nagappan, Jayanthi
Ishak, Zamzuri
Chin, Cheuk Weng
Tan, Soon Guan
Cheah, Suan Choo
Singh, Rajinder
author_facet Ting, Ngoot Chin
Jansen, Johannes
Nagappan, Jayanthi
Ishak, Zamzuri
Chin, Cheuk Weng
Tan, Soon Guan
Cheah, Suan Choo
Singh, Rajinder
author_sort Ting, Ngoot Chin
building UPM Institutional Repository
collection Online Access
description Clonal reproduction of oil palm by means of tissue culture is a very inefficient process. Tissue culturability is known to be genotype dependent with some genotypes being more amenable to tissue culture than others. In this study, genetic linkage maps enriched with simple sequence repeat (SSR) markers were developed for dura (ENL48) and pisifera (ML161), the two fruit forms of oil palm, Elaeis guineensis. The SSR markers were mapped onto earlier reported parental maps based on amplified fragment length polymorphism (AFLP) and restriction fragment length polymorphism (RFLP) markers. The new linkage map of ENL48 contains 148 markers (33 AFLPs, 38 RFLPs and 77 SSRs) in 23 linkage groups (LGs), covering a total map length of 798.0 cM. The ML161 map contains 240 markers (50 AFLPs, 71 RFLPs and 119 SSRs) in 24 LGs covering a total of 1,328.1 cM. Using the improved maps, two quantitative trait loci (QTLs) associated with tissue culturability were identified each for callusing rate and embryogenesis rate. A QTL for callogenesis was identified in LGD4b of ENL48 and explained 17.5% of the phenotypic variation. For embryogenesis rate, a QTL was detected on LGP16b in ML161 and explained 20.1% of the variation. This study is the first attempt to identify QTL associated with tissue culture amenity in oil palm which is an important step towards understanding the molecular processes underlying clonal regeneration of oil palm.
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spelling upm-280282016-04-22T03:50:55Z http://psasir.upm.edu.my/id/eprint/28028/ Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers Ting, Ngoot Chin Jansen, Johannes Nagappan, Jayanthi Ishak, Zamzuri Chin, Cheuk Weng Tan, Soon Guan Cheah, Suan Choo Singh, Rajinder Clonal reproduction of oil palm by means of tissue culture is a very inefficient process. Tissue culturability is known to be genotype dependent with some genotypes being more amenable to tissue culture than others. In this study, genetic linkage maps enriched with simple sequence repeat (SSR) markers were developed for dura (ENL48) and pisifera (ML161), the two fruit forms of oil palm, Elaeis guineensis. The SSR markers were mapped onto earlier reported parental maps based on amplified fragment length polymorphism (AFLP) and restriction fragment length polymorphism (RFLP) markers. The new linkage map of ENL48 contains 148 markers (33 AFLPs, 38 RFLPs and 77 SSRs) in 23 linkage groups (LGs), covering a total map length of 798.0 cM. The ML161 map contains 240 markers (50 AFLPs, 71 RFLPs and 119 SSRs) in 24 LGs covering a total of 1,328.1 cM. Using the improved maps, two quantitative trait loci (QTLs) associated with tissue culturability were identified each for callusing rate and embryogenesis rate. A QTL for callogenesis was identified in LGD4b of ENL48 and explained 17.5% of the phenotypic variation. For embryogenesis rate, a QTL was detected on LGP16b in ML161 and explained 20.1% of the variation. This study is the first attempt to identify QTL associated with tissue culture amenity in oil palm which is an important step towards understanding the molecular processes underlying clonal regeneration of oil palm. Public Library of Science 2013-01-29 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/28028/1/journal.pone.0053076.pdf Ting, Ngoot Chin and Jansen, Johannes and Nagappan, Jayanthi and Ishak, Zamzuri and Chin, Cheuk Weng and Tan, Soon Guan and Cheah, Suan Choo and Singh, Rajinder (2013) Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers. PLOS ONE, 8 (1). art. no. e53076. pp. 1-16. ISSN 1932-6203 10.1371/journal.pone.0053076
spellingShingle Ting, Ngoot Chin
Jansen, Johannes
Nagappan, Jayanthi
Ishak, Zamzuri
Chin, Cheuk Weng
Tan, Soon Guan
Cheah, Suan Choo
Singh, Rajinder
Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers
title Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers
title_full Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers
title_fullStr Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers
title_full_unstemmed Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers
title_short Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers
title_sort identification of qtls associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with ssr markers
url http://psasir.upm.edu.my/id/eprint/28028/
http://psasir.upm.edu.my/id/eprint/28028/
http://psasir.upm.edu.my/id/eprint/28028/1/journal.pone.0053076.pdf