2015
DOI: 10.1007/s12686-015-0485-8
|View full text |Cite
|
Sign up to set email alerts
|

Development of polymorphic chloroplast DNA markers for the endangered tree Eusideroxylon zwageri through chloroplast isolation and next-generation sequencing

Abstract: Borneo ironwood (Eusideroxylon zwageri) is a tall tropical tree that is threatened by illegal logging and exploitation due to its economic value. In the present study, approximately 10,618 bp of E. zwageri chloroplast DNA were sequenced genome-wide and 16 polymorphic markers of chloroplast DNA were developed, using next-generation sequencing technology. In total, 26 nucleotide substitutions, 3 indels, 1 sequence inversion, and 1 mononucleotide repeat variation were detected in samples of 10 trees collected fro… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
5
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
6
1

Relationship

3
4

Authors

Journals

citations
Cited by 8 publications
(6 citation statements)
references
References 11 publications
0
5
0
Order By: Relevance
“…In this study, we detected 21 chloroplast haplotypes from nine populations ( Table 1 and Figure 1) using our previously developed chloroplast DNA markers [9]. Previously, several studies have examined the genetic distribution of tropical woody species through the analysis of chloroplast haplotypes.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In this study, we detected 21 chloroplast haplotypes from nine populations ( Table 1 and Figure 1) using our previously developed chloroplast DNA markers [9]. Previously, several studies have examined the genetic distribution of tropical woody species through the analysis of chloroplast haplotypes.…”
Section: Discussionmentioning
confidence: 99%
“…The extracted DNA was stored at 4 • C until further analysis. Six chloroplast DNA regions (Ez_Cp_01, Ez_Cp_05, Ez_Cp_07, Ez_Cp_09, Ez_Cp_11, and Ez_Cp_12; [9], see Supplementary S2) were amplified by PCR, as described in [10]. Finally, chloroplast DNA sequencing reactions were performed as described in [10], using an ABI 3100 Genetic Analyzer (Thermo Fisher Scientific K.K., Kanagawa, Japan).…”
Section: Dna Extraction and Chloroplast Dna Sequencingmentioning
confidence: 99%
“…DNA fragments, approximately 200 bp in length, were sequenced using an Ion Proton TM Sequencer (Applied Biosystems, Waltham, MA, USA). The sequences were collected as described by Kurokochi et al [ 16 ] and Sugiura et al [ 17 ]. SSRs were derived using MISA software ( ); 15 regions were selected and Primer3Plus software [ 18 ] was used to design primers for these SSRs ( Supplementary 1 ).…”
Section: Methodsmentioning
confidence: 99%
“…PCR products were adjusted essentially in accordance with Ion 16S Metagenomics kit (Thermo Fisher Scientific), however, the number of cycles for amplifying the library was 30 in this study. The amplified DNAs were set to an IonPGM sequencer (Thermo Fisher Scientific) according to Kurokochi et al (2015).…”
Section: Soil Dna Extraction Pyrosequencing and Community Analysismentioning
confidence: 99%