Construction of molecule markers for prolific oil palm tissue culture; [Pembinaan Penanda Molekul bagi Kultur Tisu Kelapa Sawit Prolifik]

The use of DNA marker could minimize problems in tissue culture especially when applied during the selection of plants for tissue culture. Therefore, the aimed of this research was to develop molecular markers for prolific oil palm tissue culture using amplified fragment length polymorphism (AFLP) t...

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Published in:Sains Malaysiana
Main Author: Karim S.K.A.; Sidik N.M.
Format: Article
Language:Malay
Published: Penerbit Universiti Kebangsaan Malaysia 2018
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053613087&doi=10.17576%2fjsm-2018-4708-09&partnerID=40&md5=7f31cf318840b8312f415d7cfdbeb418
id 2-s2.0-85053613087
spelling 2-s2.0-85053613087
Karim S.K.A.; Sidik N.M.
Construction of molecule markers for prolific oil palm tissue culture; [Pembinaan Penanda Molekul bagi Kultur Tisu Kelapa Sawit Prolifik]
2018
Sains Malaysiana
47
8
10.17576/jsm-2018-4708-09
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053613087&doi=10.17576%2fjsm-2018-4708-09&partnerID=40&md5=7f31cf318840b8312f415d7cfdbeb418
The use of DNA marker could minimize problems in tissue culture especially when applied during the selection of plants for tissue culture. Therefore, the aimed of this research was to develop molecular markers for prolific oil palm tissue culture using amplified fragment length polymorphism (AFLP) technique. AFLP analysis was carried out upon 20 oil palm clones that have divided into three classes which are non-prolific clone (10 types of clone), normal clone (6 types of clone) and prolific clone (4 types of clone). All of the clones used were from different cell line. There were 25 primer combinations used in the AFLP analysis and 13 out of them have produced significant polymorphic amplification patterns. From these results, 44 polymorphic DNA fragments were isolated where 33 fragments for non-prolific clone, one fragment for normal clone and 10 fragments for prolific clone. These fragments were cloned into plasmid, sequenced and then sequence analysis was done. There were 36 polymorphic fragments have undergone the subsequent experiments. A pair of specific primers for each fragment was designed based on their sequences. The expected size of amplified DNA bands for each primer pair was between 70 bp to 500 bp. The optimized primer pairs were tested to the 20 types of oil palm clones in order to confirm the markers developed. From the 36 designated primers combinations, 2 pairs of the primers showed the potential to be used as marker for prolific oil palm tissue culture. © 2018 Penerbit Universiti Kebangsaan Malaysia. All Rights Reserved.
Penerbit Universiti Kebangsaan Malaysia
1266039
Malay
Article
All Open Access; Gold Open Access
author Karim S.K.A.; Sidik N.M.
spellingShingle Karim S.K.A.; Sidik N.M.
Construction of molecule markers for prolific oil palm tissue culture; [Pembinaan Penanda Molekul bagi Kultur Tisu Kelapa Sawit Prolifik]
author_facet Karim S.K.A.; Sidik N.M.
author_sort Karim S.K.A.; Sidik N.M.
title Construction of molecule markers for prolific oil palm tissue culture; [Pembinaan Penanda Molekul bagi Kultur Tisu Kelapa Sawit Prolifik]
title_short Construction of molecule markers for prolific oil palm tissue culture; [Pembinaan Penanda Molekul bagi Kultur Tisu Kelapa Sawit Prolifik]
title_full Construction of molecule markers for prolific oil palm tissue culture; [Pembinaan Penanda Molekul bagi Kultur Tisu Kelapa Sawit Prolifik]
title_fullStr Construction of molecule markers for prolific oil palm tissue culture; [Pembinaan Penanda Molekul bagi Kultur Tisu Kelapa Sawit Prolifik]
title_full_unstemmed Construction of molecule markers for prolific oil palm tissue culture; [Pembinaan Penanda Molekul bagi Kultur Tisu Kelapa Sawit Prolifik]
title_sort Construction of molecule markers for prolific oil palm tissue culture; [Pembinaan Penanda Molekul bagi Kultur Tisu Kelapa Sawit Prolifik]
publishDate 2018
container_title Sains Malaysiana
container_volume 47
container_issue 8
doi_str_mv 10.17576/jsm-2018-4708-09
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053613087&doi=10.17576%2fjsm-2018-4708-09&partnerID=40&md5=7f31cf318840b8312f415d7cfdbeb418
description The use of DNA marker could minimize problems in tissue culture especially when applied during the selection of plants for tissue culture. Therefore, the aimed of this research was to develop molecular markers for prolific oil palm tissue culture using amplified fragment length polymorphism (AFLP) technique. AFLP analysis was carried out upon 20 oil palm clones that have divided into three classes which are non-prolific clone (10 types of clone), normal clone (6 types of clone) and prolific clone (4 types of clone). All of the clones used were from different cell line. There were 25 primer combinations used in the AFLP analysis and 13 out of them have produced significant polymorphic amplification patterns. From these results, 44 polymorphic DNA fragments were isolated where 33 fragments for non-prolific clone, one fragment for normal clone and 10 fragments for prolific clone. These fragments were cloned into plasmid, sequenced and then sequence analysis was done. There were 36 polymorphic fragments have undergone the subsequent experiments. A pair of specific primers for each fragment was designed based on their sequences. The expected size of amplified DNA bands for each primer pair was between 70 bp to 500 bp. The optimized primer pairs were tested to the 20 types of oil palm clones in order to confirm the markers developed. From the 36 designated primers combinations, 2 pairs of the primers showed the potential to be used as marker for prolific oil palm tissue culture. © 2018 Penerbit Universiti Kebangsaan Malaysia. All Rights Reserved.
publisher Penerbit Universiti Kebangsaan Malaysia
issn 1266039
language Malay
format Article
accesstype All Open Access; Gold Open Access
record_format scopus
collection Scopus
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