Phylogenetic analysis of eleven Malaysian rice cultivars using a chloroplastic DNA marker
To date, both the morphological and molecular characteristics of Malaysian rice cultivars are not well documented resulting in difficulty to identify cultivars with specific origin or traits. Although some rice information are available, the information are mostly not systematically organized with l...
Saved in:
主要作者: | |
---|---|
格式: | Thesis |
语言: | English |
出版: |
2014
|
主题: | |
在线阅读: | http://eprints.utm.my/id/eprint/48576/1/FikriFauziMFBME2014.pdf |
标签: |
添加标签
没有标签, 成为第一个标记此记录!
|
id |
my-utm-ep.48576 |
---|---|
record_format |
uketd_dc |
spelling |
my-utm-ep.485762020-02-05T01:22:37Z Phylogenetic analysis of eleven Malaysian rice cultivars using a chloroplastic DNA marker 2014 Fauzi, Fikri QK Botany To date, both the morphological and molecular characteristics of Malaysian rice cultivars are not well documented resulting in difficulty to identify cultivars with specific origin or traits. Although some rice information are available, the information are mostly not systematically organized with limited accessibility. Thus in this work, a chloroplastic DNA (cpDNA) marker gene, the large subunit of ribulose- 1,5 - bisphosphate carboxylase (rbcL) gene were used to construct a phylogenetic tree of eleven Malaysian rice (Oryza sativa L.) cultivars. cpDNA is most commonly used in phylogenetic and barcoding study for plant species because of its high success rate in PCR amplification, appropiate length and a base substitution rate for inferring phylogeny at higher levels. The rbcL gene was amplified from genomic DNA of the 11 rice cultivars, cloned and sequenced. The sequences obtained was analyzed and aligned using software MEGA 6. Then, the phylogenetic analysis was constructed by using method Maximum Parsimony. The result revealed that rbcL gene of eleven Malaysian rice cultivars are ~1400 bp in size. Based on the tree constructed, the eleven Malaysian rice cultivars studied can be classified into two major clades. The first clade consists of MR 220 CL2, MR 219, Putih and Wai while MR 269, MR 263, MR 220, Merah Udang, Pulut Bukit, MR Q76 and Bukit Hitam falled into the second clade. Bootstrap support (BS) value in some of the branches were a bit low and these value is reflected by the small number of informative character (844 were conserved and 319 were potentially informative) to design the tree. The formation of several subclades in the tree is due to its similar genetic pattern and thus support the system classification. In overall, this study suggested that rbcL gene can serve as a good candidate gene to distinguish the phylogenetic relationship in Malaysian rice cultivars. 2014 Thesis http://eprints.utm.my/id/eprint/48576/ http://eprints.utm.my/id/eprint/48576/1/FikriFauziMFBME2014.pdf application/pdf en public http://dms.library.utm.my:8080/vital/access/manager/Repository/vital:83245?queryType=vitalDismax&query=Phylogenetic+analysis+of+eleven+Malaysian+rice+cultivars+using+a+chloroplastic+DNA+marker&public=true masters Universiti Teknologi Malaysia, Faculty of Bioscience and Medical Engineering Faculty of Bioscience and Medical Engineering |
institution |
Universiti Teknologi Malaysia |
collection |
UTM Institutional Repository |
language |
English |
topic |
QK Botany |
spellingShingle |
QK Botany Fauzi, Fikri Phylogenetic analysis of eleven Malaysian rice cultivars using a chloroplastic DNA marker |
description |
To date, both the morphological and molecular characteristics of Malaysian rice cultivars are not well documented resulting in difficulty to identify cultivars with specific origin or traits. Although some rice information are available, the information are mostly not systematically organized with limited accessibility. Thus in this work, a chloroplastic DNA (cpDNA) marker gene, the large subunit of ribulose- 1,5 - bisphosphate carboxylase (rbcL) gene were used to construct a phylogenetic tree of eleven Malaysian rice (Oryza sativa L.) cultivars. cpDNA is most commonly used in phylogenetic and barcoding study for plant species because of its high success rate in PCR amplification, appropiate length and a base substitution rate for inferring phylogeny at higher levels. The rbcL gene was amplified from genomic DNA of the 11 rice cultivars, cloned and sequenced. The sequences obtained was analyzed and aligned using software MEGA 6. Then, the phylogenetic analysis was constructed by using method Maximum Parsimony. The result revealed that rbcL gene of eleven Malaysian rice cultivars are ~1400 bp in size. Based on the tree constructed, the eleven Malaysian rice cultivars studied can be classified into two major clades. The first clade consists of MR 220 CL2, MR 219, Putih and Wai while MR 269, MR 263, MR 220, Merah Udang, Pulut Bukit, MR Q76 and Bukit Hitam falled into the second clade. Bootstrap support (BS) value in some of the branches were a bit low and these value is reflected by the small number of informative character (844 were conserved and 319 were potentially informative) to design the tree. The formation of several subclades in the tree is due to its similar genetic pattern and thus support the system classification. In overall, this study suggested that rbcL gene can serve as a good candidate gene to distinguish the phylogenetic relationship in Malaysian rice cultivars. |
format |
Thesis |
qualification_level |
Master's degree |
author |
Fauzi, Fikri |
author_facet |
Fauzi, Fikri |
author_sort |
Fauzi, Fikri |
title |
Phylogenetic analysis of eleven Malaysian rice cultivars using a chloroplastic DNA marker |
title_short |
Phylogenetic analysis of eleven Malaysian rice cultivars using a chloroplastic DNA marker |
title_full |
Phylogenetic analysis of eleven Malaysian rice cultivars using a chloroplastic DNA marker |
title_fullStr |
Phylogenetic analysis of eleven Malaysian rice cultivars using a chloroplastic DNA marker |
title_full_unstemmed |
Phylogenetic analysis of eleven Malaysian rice cultivars using a chloroplastic DNA marker |
title_sort |
phylogenetic analysis of eleven malaysian rice cultivars using a chloroplastic dna marker |
granting_institution |
Universiti Teknologi Malaysia, Faculty of Bioscience and Medical Engineering |
granting_department |
Faculty of Bioscience and Medical Engineering |
publishDate |
2014 |
url |
http://eprints.utm.my/id/eprint/48576/1/FikriFauziMFBME2014.pdf |
_version_ |
1747817424170778624 |