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91 results for “chloroplast genome”
FIGURE 1 in Complete chloroplast genomes of Archiclematis, Naravelia and Clematis (Ranunculaceae), and their phylogenetic implications
FIGURE 1. Map of the chloroplast genomes of Clematis s.l. Genes shown outside the circle are transcribed clockwise, whereas those inside the circle are transcribed counterclockwise. Genes belonging to different functional groups are colored. The dashed area in the inner circle indicates the GC content of the plastomes.
FIGURE 5 in Complete chloroplast genomes of Archiclematis, Naravelia and Clematis (Ranunculaceae), and their phylogenetic implications
FIGURE 5. Analyses of repeated sequences in Clematis s.l. chloroplast genomes. A: Number of each repeat type; B: frequency of direct repeats by length; C: frequency of reverse repeats by length; D: frequency of palindromic repeats by length; E: location of repeats.
FIGURE 2 in Complete chloroplast genomes of Archiclematis, Naravelia and Clematis (Ranunculaceae), and their phylogenetic implications
FIGURE 2. Comparison of the LSC, IRs and SSC borders among Clematis s.l. samples used in this study.
Phylogeny of Crataegus (Rosaceae) based on 257 nuclear loci and chloroplast genomes: evaluating the impact of hybridization
<p>Assembled sequence alignments and phylogenetic trees for plastomes and nuclear loci for 24 samples of Crataegus.</p>
Comparative Analysis of Complete Chloroplast Genomes and Multiple DNA Sequences Reveals Interspecific Relationships of C. bretschneideri and Related Species in China
<p><strong> ITS, and <em>LEAFY</em> intron 1 sequencing of 36 Crataegus accessions.</strong></p>
Rhizophora complete chloroplast genome sequences
<p>Historical processes of long-distance migration and ocean-wide expansion feature the global biogeographic pattern of <i>Rhizophora</i> species. Throughout the Indian Ocean, <i>R. stylosa</i> and <i>R. mucronata</i> appear as a young phylogenetic group with expansion of <i>R. mucronata</i> towards the Western Indian Ocean (WIO) driven by the South Equatorial Current. Nuclear microsatellites revealed genetic patterns and breaks, however, estimating propagule dispersal routes requires maternally inherited cytoplasmic markers. Here, we examine the phylogeography of 21 <i>R. mucronata</i> provenances across a >4,200 km coastal stretch in the WIO using <i>R. stylosa</i> as outgroup. Full length chloroplast genome (164,474 bp) and nuclear ribosomal RNA cistron (8,033 bp) sequences were assembled. Boundaries, junction point, sequence orientation and stretch between LSC/IRb/SSC/IRa/LSC showed no differences with the <i>R. stylosa</i> chloroplast genome. A total of 58 mutations in <i>R. mucronata</i> encompassing transitions/transversions, insertion-deletions and mononucleotide repeats revealed three major haplogroups. Haplonetwork, Bayesian ML and Approximate Bayesian Computation (ABC) analyses supported discrete historical migration events. An ancient haplogroup A in the Seychelles and eastern Madagascar was as divergent from other <i>R. mucronata</i> haplogroups as it was from <i>R. stylosa</i>. A star-like haplonetwork referred to recent range expansion of haplogroup B from northern Madagascar towards the African mainland coastline, including a single variant spanning >1,800 km across the Mozambique Channel Area. Populations south of Delagoa Bight contained haplogroup C and originate from a unique bottleneck dispersal event. Divergence estimates of pre- and post-Last Glacial Maximum illustrated a recent emergence of WIO <i>Rhizophora </i>mangroves compared to other oceans. Connectivity patterns could be aligned with directionality of major ocean currents. Madagascar and the Seychelles each harbored haplogroups A and B, albeit among spatially separated populations, explained from a different migration era. Likewise, the Aldabra Atoll harbored spatially distinct haplotypes. Nuclear ribosomal cistron (8,033bp) variants corresponded to haplogroups and confirmed admixtures in the Seychelles and Aldabra. These findings shed new light on the origins and dispersal routes of <i>R. mucronata</i> lineages that have shaped their contemporary populations in large regions of the WIO, which may be important information for defining marine conservation units, both at ocean scale and at level of small islands.</p>
Comparative Analysis of Complete Chloroplast Genomes of 13 Species in Epilobium, Circaea, and Chamaenerion and Insights into Phylogenetic Relationships of Onagraceae
<p>This is all the alignments which used to constructed a phylogenetic tree in our study about Onagraceae. The evening primrose family, Onagraceae, is a well defined family of the order Myrtales, which comprises 22 genera widely distributed from boreal to tropical areas. In the present study, we report and characterize the complete chloroplast genome sequences of 13 species in <em>Circaea</em>,<em> Chamaenerion</em>, and <em>Epilobium</em> using a next-generation sequencing method. We also retrieved plastome sequences from two other Onagraceae genera to characterize the chloroplast genome of the family. The complete plastomes of Onagraceae showed a typical quadripartite structure and encoded an identical set of 112 genes (with exclusion of duplication), including 78 protein-coding genes, 30 transfer RNAs, and four ribosomal RNAs. The results show that chloroplast genomes are basically conserved in gene arrangement across the family. Whereas, a large segment of inversion was detected in the LSC region of all samples in the<em> Oenothera </em>subsect. <em>Oenothera</em>. An inverted repeat (IR) contraction was found in <em>Circaea</em> and<em> Ludwigia </em>samples. We also compared chloroplast genomes across the Onagraceae samples and revealed similarities in some features, including nucleotide content, codon usage, RNA editing sites, and simple sequence repeats (SSRs). Phylogeny was inferred by the chloroplast genome data using maximum-likelihood (ML) and Bayesian inference (BI) methods. The generic relationship of Onagraceae was well resolved by the complete plastome sequences, showing potential value in inferring phylogeny within the family. <em>Oenothera </em>phylogeny was better resolved than other densely sampled genera. Biparental transmission may be the main cause of higher variation in the genus<em> Oenothera</em>.</p>
Chloroplast genome of the invasive Pyrus calleryana
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Data from: Identification of chloroplast genome loci suitable for high-resolution phylogeographic studies of Colocasia esculenta (L.) Schott (Araceae) and closely related taxa
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Data from: Assemblage Accumulation Curves: A framework for resolving species accumulation in biological communities using chloroplast genome sequences
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Genome-wide RAD sequencing resolves the evolutionary history of serrate leaf Juniperus and reveals discordance with chloroplast phylogeny
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Complete chloroplast genomes of Desmidorchis penicillata (Deflers) Plowes and Desmidorchis retrospiciens Ehrenb: Comparative and phylogenetic analyses among subtribe Stapeliinae (Ceropegieae, Asclepiadoideae, Apocynaceae)
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Rhizophora complete chloroplast genome sequences
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Figure 3 from: Maurin KJL (2020) A dated phylogeny of the genus Pennantia (Pennantiaceae) based on whole chloroplast genome and nuclear ribosomal 18S–26S repeat region sequences. PhytoKeys 155: 15-32. https://doi.org/10.3897/phytokeys.155.53460
Figure 3 Undated 18S–26S nuclear DNA repeat region BEAST 2 phylogeny of Pennantia, under the Birth-Death model. The tree was rooted to make P. cunninghamii sister to the other species of Pennantia, in accordance with the chloroplast DNA tree and the ITS tree of Keeling et al. (2004). Node posterior probability is shown next to the corresponding node. The sequences downloaded from GenBank have their accession number in round brackets; the others were generated from the samples used in this study.
Supplementary material 2 from: Maurin KJL (2020) A dated phylogeny of the genus Pennantia (Pennantiaceae) based on whole chloroplast genome and nuclear ribosomal 18S–26S repeat region sequences. PhytoKeys 155: 15-32. https://doi.org/10.3897/phytokeys.155.53460
BEAST2 and RAxML files
Figure 2 from: Maurin KJL (2020) A dated phylogeny of the genus Pennantia (Pennantiaceae) based on whole chloroplast genome and nuclear ribosomal 18S–26S repeat region sequences. PhytoKeys 155: 15-32. https://doi.org/10.3897/phytokeys.155.53460
Figure 2 Dated chloroplast DNA BEAST 2 phylogeny of Pennantia, under the Birth-Death model. Mean node age and 95% HPD (in My) is given in the table embedded in the figure under the corresponding letter code. 95% HPD is also represented by blue bars. All node posterior probabilities are equal to 1 except if indicated otherwise. The calibrated nodes (see text) are indicated by red dots.
Supplementary material 1 from: Maurin KJL (2020) A dated phylogeny of the genus Pennantia (Pennantiaceae) based on whole chloroplast genome and nuclear ribosomal 18S–26S repeat region sequences. PhytoKeys 155: 15-32. https://doi.org/10.3897/phytokeys.155.53460
Figs S1–S5; Tables S1–S3
Figure 1 from: Maurin KJL (2020) A dated phylogeny of the genus Pennantia (Pennantiaceae) based on whole chloroplast genome and nuclear ribosomal 18S–26S repeat region sequences. PhytoKeys 155: 15-32. https://doi.org/10.3897/phytokeys.155.53460
Figure 1 General distribution of the four Pennantia species. TKI = Three Kings Islands. Generated in QGIS 3.0.1 from Google Satellite data obtained through the XYZ Tiles tool (https://mt1.google.com/vt/lyrs=s&x={x}&y={y}&z={z}).
Evolution of Rosaceae chloroplast genomes highlights unique Cerasus diversification and independent origins of fruit cherry
<p>Rosaceae plants comprise numerous fruit crops with huge economic values. The lack of genomic characteristics has largely blocked our understanding about the Rosaceae gene and plastome evolution. Here, we analyzed 121 Rosaceae chloroplast (cp) genomes of 51 taxa from 19 genera, predominantly including the Cerasus plants and their relatives. To our knowledge, we generated the first comprehensive map of genomic variation across Rosaceae plastomes. Protein-coding genes of Rosaceae plastomes were characterized with high proportion (over 50%) of synonymous variants and InDels with multiple triplets. Four photosynthesis-related genes were under Darwin selection, which are unique in woody fruit trees of Rosaceae. We detected considerable variations in genome size among Rosaceae plastomes and observed trivial and obvious structural variation in the examined cp genomes of tribes Pyrodae and Amygdaleae. Phylogenomic analyses and molecular dating highlighted the independent evolution of true cherry, dwarf cherry and relatives. Our findings strongly support to taxonomically treat the monophyletic true cherry group as a separate genus excluding dwarf cherry. High levels of genomic differentiation and distinct phylogenetic relationships implied independent origins and domestication between fruit cherries, particularly between cultivated Cerasus psuedocerasus and Cerasus avium. We further proposed an evolutionary model to elucidate multiple genomic introgression events among true cherries occurring since ~15 Mya. Well-resolved maternal phylogeny suggested that the cultivated C. pseudocerasus might be originated from Longmenshan Fault zone, the eastern edge of Himalaya-Hengduan Mountains, where they have subjected to frequent genomic introgression between its presumed wild ancestors and other close relatives. In conclusion, comparative analyses of plastomes and chloroplast genes detected diverse evolutionary behaviors and divergent adaptive selection in Rosaceae. We provide robust evidences for the independent origins and domestication of fruit cherries.</p>
Data from: Congruent deep relationships in the grape family (Vitaceae) based on sequences of chloroplast genomes and mitochondrial genes via genome skimming
Vitaceae is well-known for having one of the most economically important fruits, i.e., the grape (Vitis vinifera). The deep phylogeny of the grape family was not resolved until a recent phylogenomic analysis of 417 nuclear genes from transcriptome data. However, it has been reported extensively that topologies based on nuclear and organellar genes may be incongruent due to differences in their evolutionary histories. Therefore, it is important to reconstruct a backbone phylogeny of the grape family using plastomes and mitochondrial genes. In this study, next-generation sequencing data sets of 27 species were obtained using genome skimming with total DNAs from silica-gel preserved tissue samples on an Illumina HiSeq 2500 instrument. Plastomes were assembled using the combination of de novo and reference genome (of V. vinifera) methods. Sixteen mitochondrial genes were also obtained via genome skimming using the reference genome of V. vinifera. Extensive phylogenetic analyses were performed using maximum likelihood and Bayesian methods. The topology based on either plastome data or mitochondrial genes is congruent with the one using hundreds of nuclear genes, indicating that the grape family did not exhibit significant reticulation at the deep level. The results showcase the power of genome skimming in capturing extensive phylogenetic data: especially from chloroplast and mitochondrial DNAs.
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Allen Brain Atlas
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