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The Chloroplast Genomes of Four Bupleurum (Apiaceae) Species Endemic to Southwestern China, a Diversity Center of the Genus, As Well As Their Evolutionary Implications and Phylogenetic Inferences

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2021 Oct 3
PMID 34600494
Citations 20
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Abstract

Background: As one of the largest genera in Apiaceae, Bupleurum L. is well known for its high medicinal value. The genus has frequently attracted the attention of evolutionary biologist and taxonomist for its distinctive characteristics in the Apiaceae family. Although some chloroplast genomes data have been now available, the changes in the structure of chloroplast genomes and selective pressure in the genus have not been fully understood. In addition, few of the species are endemic to Southwest China, a distribution and diversity center of Chinese Bupleurum. Endemic species are key components of biodiversity and ecosystems, and investigation of the chloroplast genomes features of endemic species in Bupleurum will be helpful to develop a better understanding of evolutionary process and phylogeny of the genus. In this study, we analyzed the sequences of whole chloroplast genomes of 4 Southwest China endemic Bupleurum species in comparison with the published data of 17 Bupleurum species to determine the evolutionary characteristics of the genus and the phylogenetic relationships of Asian Bupleurum.

Results: The complete chloroplast genome sequences of the 4 endemic Bupleurum species are 155,025 bp to 155,323 bp in length including a SSC and a LSC region separated by a pair of IRs. Comparative analysis revealed an identical chloroplast gene content across the 21 Bupleurum species, including a total of 114 unique genes (30 tRNA genes, 4 rRNA genes and 80 protein-coding genes). Chloroplast genomes of the 21 Bupleurum species showed no rearrangements and a high sequence identity (96.4-99.2%). They also shared a similar tendency of SDRs and SSRs, but differed in number (59-83). In spite of their high conservation, they contained some mutational hotspots, which can be potentially exploited as high-resolution DNA barcodes for species discrimination. Selective pressure analysis showed that four genes were under positive selection. Phylogenetic analysis revealed that the 21 Bupleurum formed two major clades, which are likely to correspond to their geographical distribution.

Conclusions: The chloroplast genome data of the four endemic Bupleurum species provide important insights into the characteristics and evolution of chloroplast genomes of this genu, and the phylogeny of Bupleurum.

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References
1.
Tillich M, Lehwark P, Pellizzer T, Ulbricht-Jones E, Fischer A, Bock R . GeSeq - versatile and accurate annotation of organelle genomes. Nucleic Acids Res. 2017; 45(W1):W6-W11. PMC: 5570176. DOI: 10.1093/nar/gkx391. View

2.
Shaw J, Shafer H, Leonard O, Kovach M, Schorr M, Morris A . Chloroplast DNA sequence utility for the lowest phylogenetic and phylogeographic inferences in angiosperms: the tortoise and the hare IV. Am J Bot. 2014; 101(11):1987-2004. DOI: 10.3732/ajb.1400398. View

3.
Castellanos-Morales G, Gamez N, Castillo-Gamez R, Eguiarte L . Peripatric speciation of an endemic species driven by Pleistocene climate change: The case of the Mexican prairie dog (Cynomys mexicanus). Mol Phylogenet Evol. 2015; 94(Pt A):171-81. DOI: 10.1016/j.ympev.2015.08.027. View

4.
Dong W, Liu J, Yu J, Wang L, Zhou S . Highly variable chloroplast markers for evaluating plant phylogeny at low taxonomic levels and for DNA barcoding. PLoS One. 2012; 7(4):e35071. PMC: 3325284. DOI: 10.1371/journal.pone.0035071. View

5.
Drescher A, Ruf S, Calsa Jr T, Carrer H, Bock R . The two largest chloroplast genome-encoded open reading frames of higher plants are essential genes. Plant J. 2000; 22(2):97-104. DOI: 10.1046/j.1365-313x.2000.00722.x. View