Fig 1.
Map of the L. dussii plastome.
Genes (exons are denoted as closed boxes) on the outside of the outermost circle are transcribed in the counter clockwise direction, while genes on the inside of this circle are transcribed in the clockwise direction. Structural components are labeled on the inner circle as LSC and SSC regions, IRA and IRB. Inner graph charts % GC content across the genome. A color-coded scale classifies the genes into functional categories.
Table 1.
Summary table of the genes present in hornwort plastomes, + gene presence, ψ pseudogene.
Fig 2.
Map of the L. dussii mitogenome.
Genes (exons indicated as closed boxes) on the outside of the circle are transcribed in the clockwise direction, and genes on the inside of the circle are transcribed in the counter clockwise direction. Pseudogenes are marked with a ψ. A color-coded scale classifies the genes into functional categories.
Table 2.
Summary table of the genes present in hornwort mitogenomes, + gene presence, ψ pseudogene.
Table 3.
Nature and density of RNA edited sites in the organellar genomes of Leiosporoceros and other hornworts.
Fig 3.
Functional consequence and efficiency of RNA editing in the protein-coding regions of L. dussii plastid and mitochondrial transcripts.
The edited sites were classified into three categories: conservative (when the editing events improved sequence conservation to orthologous proteins from green algae or other land plants), non-conservative (when they reduced sequence conservation), and synonymous or silent sites (when the amino acids corresponding to these sites were not altered).
Table 4.
Conversion of amino acids resulting from RNA editing in the plastome and mitogenome of L. dussii.