Examinando por Materia "Chloroplast genome"

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Chloroplast genome of Tillandsia landbeckii Phil. (Bromeliaceae) a species adapted to the hyper-arid conditions of the Atacama and Peruvian desert
(Taylor & Francis, 2021-11-10) Chávez Galarza, Julio César; Cardenas Ninasivincha, Stefanny; Contreras, Roberto; Ferro Mauricio, Rubén Darío; Huanca Mamani, Wilson
Tillandsia landbeckii Phil. is a vulnerable species belonging to the terrestrial Bromeliaceae family; it is highly adapted to extremely hyper-arid conditions of the Atacama Desert and Peruvian deserts. In this study, we sequenced, assembled, and annotated its chloroplast genome. T. landbeckii chloroplast genome is 159,131 bp in length, containing a large single-copy region of 87,164 bp, a small single-copy region of 18,521 bp, and a pair of inverted repeat regions of 26,723 bp. The GC content of the chloroplast genome is 37.33%. It encodes a total of 132 genes, including 86 protein-coding genes, 38 tRNA genes and 8 rRNA genes. The phylogenetic tree indicates that T. landbeckii is placed within the Bromeliaceae family and has a close relationship with T. marconae with 100% support.
Chloroplast genome of Tillandsia marconae till & Vitek (Bromeliaceae), a hyperarid desert endangered species
(Taylor & Francis, 2021-08-20) Chávez Galarza, Julio César; Cardenas Ninasivincha, Stefanny; Contreras, Roberto; Ferro Mauricio, Rubén Darío; Huanca Mamani, Wilson
Tillandsia marconae Till & Vitek (Bromeliaceae) is a rare plant native species that grows over sand, in the coastal desert from Perú and Chile and is considered an endangered species. In this study, we assembled its chloroplast genome. The draft chloroplast genome of T. marconae is ca. 158,873 bp in length, containing a large single-copy region of 86,937 bp, a small single-copy region of 18,506 bp, and a pair of inverted repeat regions of 26,715 bp. The GC content of the draft chloroplast genome is 37.4%. It encodes a total of 135 genes, including 86 protein-coding genes, 38 tRNA genes, 8 rRNA genes, and three pseudogenes. The phylogenetic tree indicated that T. marconae is placed within the Bromeliaceae family and a close relationship with Tillandsia usneoides with 100% support.
Decoding the chloroplast genome of the Amazonian fruit Myrciaria dubia (camu-camu): molecular evolution and comparative genomics across the order Myrtales
(Springer Nature, 2026-08-14) Castro, Juan C.; Leonardo, Diego A.; Cobos, Marianela; Vargas, Jhon A.; Paredes, Jae D.; Adrianzén, Pedro M.; Castro, Carlos G.; Imán Correa, Sixto Alfredo; Rodriguez, Hicler N.; Marapara, Jorge L.; Maddox , J. Dylan
Myrciaria dubia (camu-camu) is an economically important Amazonian fruit species with severely limited genomic resources despite growing commercial interest and conservation needs. This study sequenced, assembled, and comprehensively analyzed the complete chloroplast (cp) genome of M. dubia and performed comparative genomic analyses across the order Myrtales, including codon usage, codon decoding mechanisms, repetitive elements, nucleotide diversity, and phylogenetic reconstruction. The cp genome spanned 158,664 bp with a typical quadripartite organization: a large single-copy region (LSC = 87,640 bp), a small single-copy region (SSC = 18,324 bp), and paired inverted repeats (IRA/IRB = 26,350 bp each). Functional annotation identified 135 genomic features, comprising 84 protein-coding genes, 37 tRNA genes, eight rRNA genes, and five pseudogenes. Codon usage analysis revealed a strong AT bias (62.50%), with 30 preferred codons (RSCU >1.0) predominantly ending with A/T nucleotides. Codon decoding analysis assigned all 61 sense codons to five mechanistic categories, collectively achieving complete codon coverage across all 23 Myrtales accessions. Repetitive element analysis identified 69 simple sequence repeats in M. dubia (91.3% mononucleotide, predominantly adenine motifs in LSC intergenic spacers) and 439 long dispersed repeat pairs (97.5% palindromic, concentrated in the inverted repeat regions). Nucleotide diversity varied significantly across structural regions (SSC, mean π = 0.173; LSC, mean π = 0.084; IRA/IRB, mean π = 0.010–0.015), with the highest diversity window (π = 0.240) located in the SSC at approximately 117.7 kb. SWAN analysis of 78 protein-coding genes identified rpl22, ycf1, matK, ndhF, and ndhD as the most variable loci, with no gene exceeding ω = 1.0, indicating a pervasive purifying selection. Comparative analysis across 19 Myrtaceae accessions demonstrated complete gene collinearity and conserved IR boundary arrangement, with divergence concentrated in the SSC intergenic regions. Phylogenetic analysis positioned M. dubia as a sister species to Plinia trunciflora within the Myrteae tribe, nested in a well-supported monophyletic Myrtaceae clade (bootstrap = 100%).