| http://purl.uniprot.org/citations/31233545 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/31233545 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/31233545 | http://www.w3.org/2000/01/rdf-schema#comment | "Recent plastid genome (plastome) studies of legumes (family Fabaceae) have shown that this family has undergone multiple atypical plastome evolutions from each of the major clades. The tribe Desmodieae belongs to the Phaseoloids, an important but systematically puzzling clade within Fabaceae. In this study, we investigated the plastome evolution of Desmodieae and analyzed its phylogenetic signaling. We sequenced six complete plastomes from representative members of Desmodieae and from its putative sister Phaseoloid genus Mucuna. Those genomes contain 128 genes and range in size from 148,450 to 153,826 bp. Analyses of gene and intron content revealed similar characters among the members of Desmodieae and Mucuna. However, there were also several distinct characters identified. The loss of the rpl2 intron was a feature shared between Desmodieae and Mucuna, whereas the loss of the rps12 intron was specific to Desmodieae. Likewise, gene loss of rps16 was observed in Mucuna but not in Desmodieae. Substantial sequence variation of ycf4 was detected from all the sequenced plastomes, but pseudogenization was restricted to the genus Desmodium. Comparative analysis of gene order revealed a distinct plastome conformation of Desmodieae compared with other Phaseoloid legumes, i.e., an inversion of an approximately 1.5-kb gene cluster (trnD-GUC, trnY-GUA, and trnE-UUC). The inversion breakpoint suggests that this event was mediated by the recombination of an 11-bp repeat motif. A phylogenetic analysis based on the plastome-scale data set found the tribe Desmodieae is a highly supported monophyletic group nested within the paraphyletic Phaseoleae, as has been found in previous phylogenetic studies. Two subtribes (Desmodiinae and Lespedezinae) of Desmodieae were also supported as monophyletic groups. Within the subtribe Lespedezinae, Lespedeza is closer to Kummerowia than Campylotropis."xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.org/dc/terms/identifier | "doi:10.1371/journal.pone.0218743"xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/author | "Choi B.H."xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/author | "Choi B.H."xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/author | "Choi I.S."xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/author | "Choi I.S."xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/author | "Jin D.P."xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/author | "Jin D.P."xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/date | "2019"xsd:gYear |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/date | "2019"xsd:gYear |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/name | "PLoS ONE"xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/name | "PLoS One"xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/pages | "e0218743"xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/pages | "e0218743"xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/title | "Plastid genome evolution in tribe Desmodieae (Fabaceae: Papilionoideae)."xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/title | "Plastid genome evolution in tribe Desmodieae (Fabaceae: Papilionoideae)."xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/volume | "14"xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://purl.uniprot.org/core/volume | "14"xsd:string |
| http://purl.uniprot.org/citations/31233545 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/31233545 |
| http://purl.uniprot.org/citations/31233545 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/31233545 |
| http://purl.uniprot.org/citations/31233545 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/31233545 |
| http://purl.uniprot.org/citations/31233545 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/31233545 |
| http://purl.uniprot.org/uniprot/A0A510BUX1 | http://purl.uniprot.org/core/citation | http://purl.uniprot.org/citations/31233545 |