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Chloroplast Genome Analysis for Genetic Information and Authentication in Five Barleria Species
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In order to authenticate the genomic information of Barleriacristata L., B. lupulina Lindl., B. repens Nees, B. siamensis Craib, and B. strigosa Willd, cp genomes were investigated. They revealed a general structure with a total size of 151,997–152,324 bp. The genomes encoded a total of 131 genes, including 86 CDS, 37 tRNA, and 8 rRNA genes. Other details found were as follows: different numbers and types of SSRs; identical gene content, which is adjacent to the border regions, except for B. strigosa, that revealed a shorter ndhF gene sequence and lacked the ycf1 gene; slightly different genetic distance values, which can be used for species identification; three distinct gaps of nucleotide variations between the species located at the intergenic spacer regions of the LSC and CDS of the SSC; three effective molecular markers derived from divergent hotspot regions, including the ccsA-ndhD, ndhA-ndhH-rps15, and ycf1. The genetic relationships derived from the cp genome and the CDS phylogenetic trees of Barleria and the 13 genera in Acanthaceae and different families, Scrophulariaceae and Phrymaceae, showed similar results. The six Barleria species as monophyletic groups with inner and outer outgroups were found to have perfect discrimination. These results have helped to authenticate the five Barleria species and the six genera in Acanthaceae.
Title: Chloroplast Genome Analysis for Genetic Information and Authentication in Five Barleria Species
Description:
In order to authenticate the genomic information of Barleriacristata L.
, B.
lupulina Lindl.
, B.
repens Nees, B.
siamensis Craib, and B.
strigosa Willd, cp genomes were investigated.
They revealed a general structure with a total size of 151,997–152,324 bp.
The genomes encoded a total of 131 genes, including 86 CDS, 37 tRNA, and 8 rRNA genes.
Other details found were as follows: different numbers and types of SSRs; identical gene content, which is adjacent to the border regions, except for B.
strigosa, that revealed a shorter ndhF gene sequence and lacked the ycf1 gene; slightly different genetic distance values, which can be used for species identification; three distinct gaps of nucleotide variations between the species located at the intergenic spacer regions of the LSC and CDS of the SSC; three effective molecular markers derived from divergent hotspot regions, including the ccsA-ndhD, ndhA-ndhH-rps15, and ycf1.
The genetic relationships derived from the cp genome and the CDS phylogenetic trees of Barleria and the 13 genera in Acanthaceae and different families, Scrophulariaceae and Phrymaceae, showed similar results.
The six Barleria species as monophyletic groups with inner and outer outgroups were found to have perfect discrimination.
These results have helped to authenticate the five Barleria species and the six genera in Acanthaceae.
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