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.2014 Apr;6(4):897-911.
doi: 10.1093/gbe/evu061.

Analyses of charophyte chloroplast genomes help characterize the ancestral chloroplast genome of land plants

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Analyses of charophyte chloroplast genomes help characterize the ancestral chloroplast genome of land plants

Peter Civaň et al. Genome Biol Evol.2014 Apr.

Abstract

Despite the significance of the relationships between embryophytes and their charophyte algal ancestors in deciphering the origin and evolutionary success of land plants, few chloroplast genomes of the charophyte algae have been reconstructed to date. Here, we present new data for three chloroplast genomes of the freshwater charophytes Klebsormidium flaccidum (Klebsormidiophyceae), Mesotaenium endlicherianum (Zygnematophyceae), and Roya anglica (Zygnematophyceae). The chloroplast genome of Klebsormidium has a quadripartite organization with exceptionally large inverted repeat (IR) regions and, uniquely among streptophytes, has lost the rrn5 and rrn4.5 genes from the ribosomal RNA (rRNA) gene cluster operon. The chloroplast genome of Roya differs from other zygnematophycean chloroplasts, including the newly sequenced Mesotaenium, by having a quadripartite structure that is typical of other streptophytes. On the basis of the improbability of the novel gain of IR regions, we infer that the quadripartite structure has likely been lost independently in at least three zygnematophycean lineages, although the absence of the usual rRNA operonic synteny in the IR regions of Roya may indicate their de novo origin. Significantly, all zygnematophycean chloroplast genomes have undergone substantial genomic rearrangement, which may be the result of ancient retroelement activity evidenced by the presence of integrase-like and reverse transcriptase-like elements in the Roya chloroplast genome. Our results corroborate the close phylogenetic relationship between Zygnematophyceae and land plants and identify 89 protein-coding genes and 22 introns present in the chloroplast genome at the time of the evolutionary transition of plants to land, all of which can be found in the chloroplast genomes of extant charophytes.

Keywords: bryophytes; charophytes; chloroplast genomics; land plants.

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Figures

F<sc>ig</sc>. 1.—
Fig. 1.—
Chloroplast genome maps ofKlebsormidium flaccidum (A),Mesotaenium endlicherianum (B), andRoya anglica (C).
F<sc>ig</sc>. 2.—
Fig. 2.—
IR regions ofKlebsormidium andRoya, in comparison toChaetosphaeridium andChara (charophytes), andPellia (a bryophyte).
F<sc>ig</sc>. 3.—
Fig. 3.—
Chloroplast gene content among charophytes and an inferred HLPA. All rRNA and protein-coding genes found within the sample set of the phylogenetic analyses are included. Gene presence and absence are indicated by blue and orange shading, respectively. Novel absences of genes with respect to other charophyte genomes are highlighted in red. (Note that the disambiguation ofycf2/ftsH has been newly interpreted, seesupplementary table S1,Supplementary Material online.)
F<sc>ig</sc>. 4.—
Fig. 4.—
Phylogenetic analyses. (A) Bayesian MCMC phylogenetic analyses of 83 protein-coding chloroplast genes: PhyloBayes CAT + gcpREV + Γ, marginal likelihood: −Lh = 244,645.3855. (B) Strict consensus tree of six most parsimonious trees (length 239, consistency index = 0.243, retention index = 0.786) resulting from analysis of the structural data (gene and intron content, operon structure). Numbers at nodes are posterior probabilities and nonparametric bootstrap values for (A) and (B), respectively. The nodes representing the HLPA are highlighted.
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