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. 2009 Feb 12:9:39.
doi: 10.1186/1471-2148-9-39.

Gain and loss of elongation factor genes in green algae

Affiliations

Gain and loss of elongation factor genes in green algae

Ellen Cocquyt et al. BMC Evol Biol. .

Abstract

Background: Two key genes of the translational apparatus, elongation factor-1 alpha (EF-1alpha) and elongation factor-like (EFL) have an almost mutually exclusive distribution in eukaryotes. In the green plant lineage, the Chlorophyta encode EFL except Acetabularia where EF-1alpha is found, and the Streptophyta possess EF-1alpha except Mesostigma, which has EFL. These results raise questions about evolutionary patterns of gain and loss of EF-1alpha and EFL. A previous study launched the hypothesis that EF-1alpha was the primitive state and that EFL was gained once in the ancestor of the green plants, followed by differential loss of EF-1alpha or EFL in the principal clades of the Viridiplantae. In order to gain more insight in the distribution of EF-1alpha and EFL in green plants and test this hypothesis we screened the presence of the genes in a large sample of green algae and analyzed their gain-loss dynamics in a maximum likelihood framework using continuous-time Markov models.

Results: Within the Chlorophyta, EF-1alpha is shown to be present in three ulvophycean orders (i.e., Dasycladales, Bryopsidales, Siphonocladales) and the genus Ignatius. Models describing gene gain-loss dynamics revealed that the presence of EF-1alpha, EFL or both genes along the backbone of the green plant phylogeny is highly uncertain due to sensitivity to branch lengths and lack of prior knowledge about ancestral states or rates of gene gain and loss. Model refinements based on insights gained from the EF-1alpha phylogeny reduce uncertainty but still imply several equally likely possibilities: a primitive EF-1alpha state with multiple independent EFL gains or coexistence of both genes in the ancestor of the Viridiplantae or Chlorophyta followed by differential loss of one or the other gene in the various lineages.

Conclusion: EF-1alpha is much more common among green algae than previously thought. The mutually exclusive distribution of EF-1alpha and EFL is confirmed in a large sample of green plants. Hypotheses about the gain-loss dynamics of elongation factor genes are hard to test analytically due to a relatively flat likelihood surface, even if prior knowledge is incorporated. Phylogenetic analysis of EFL genes indicates misinterpretations in the recent literature due to uncertainty regarding the root position.

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Figures

Figure 1
Figure 1
Distribution of EF-1α and EFL in the green plants. The type of elongation factor is indicated with black (EF-1α) or gray (EFL) squares. The reference phylogeny was obtained by Bayesian phylogenetic inference of nuclear SSU rDNA and the plastid genes rbcL and atpB. Numbers at nodes indicate posterior probabilities (top) and ML bootstrap values (bottom); values below respectively 0.9 and 50 are not shown.
Figure 2
Figure 2
Phylogenies inferred from EF-1α and EFL amino-acid sequences with Bayesian techniques. Sequences belonging to the green plant lineage are in gray boxes. Whereas all green plant EF-1α sequences group in a single clade, the green plant EFL sequences seem to form separate lineages. Sequences generated for this study are indicated with triangles. Numbers at nodes indicate posterior probabilities (top) and ML bootstrap values (bottom); values below respectively 0.9 and 50 are not shown.
Figure 3
Figure 3
Gain-loss dynamics of green algal elongation factor genes and their inferred presence in ancestral genomes. Gain and loss rates, as well as the estimated probabilities for presence of the genes in ancestral genomes are given for a variety of analysis conditions. Panels A-C show the outcome of models in which EF-1α and EFL gain and loss rates were not constrained. In panels D-F, the gain rate of EF-1α was constrained to be 10-6. Colors were used to visualize estimated probabilities for presence of genes along the tree. Red indicates a high probability for EF-1α, blue marks a high probability of EFL and yellow stands for a high probability of the presence of both genes. Intermediate colors indicate uncertainty.
Figure 4
Figure 4
Visualization of the posterior probability of rooting of the EFL tree. The topology represents the unrooted topology of EFL genes. Branch width is proportional to the posterior probability that the outgroup, consisting of archaebacterial EF-1α, EF-1α, eRF3 and HBS1 sequences, attaches to the ingroup tree at that point. Numbers at branches represent the total posterior probability that the root is situated along the branch in question.

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