- Research article
- Open Access
Loss of matKRNA editing in seed plant chloroplasts
BMC Evolutionary Biology volume 9, Article number: 201 (2009)
RNA editing in chloroplasts of angiosperms proceeds by C-to-U conversions at specific sites. Nuclear-encoded factors are required for the recognition of cis-elements located immediately upstream of editing sites. The ensemble of editing sites in a chloroplast genome differs widely between species, and editing sites are thought to evolve rapidly. However, large-scale analyses of the evolution of individual editing sites have not yet been undertaken.
Here, we analyzed the evolution of two chloroplast editing sites, matK-2 and matK-3, for which DNA sequences from thousands of angiosperm species are available. Both sites are found in most major taxa, including deep-branching families such as the nymphaeaceae. However, 36 isolated taxa scattered across the entire tree lack a C at one of the two matK editing sites. Tests of several exemplary species from this in silico analysis of matK processing unexpectedly revealed that one of the two sites remain unedited in almost half of all species examined. A comparison of sequences between editors and non-editors showed that specific nucleotides co-evolve with the C at the matK editing sites, suggesting that these nucleotides are critical for editing-site recognition.
(i) Both matK editing sites were present in the common ancestor of all angiosperms and have been independently lost multiple times during angiosperm evolution.
(ii) The editing activities corresponding to matK-2 and matK-3 are unstable.
(iii) A small number of third-codon positions in the vicinity of editing sites are selectively constrained independent of the presence of the editing site, most likely because of interacting RNA-binding proteins.
Chloroplast RNA metabolism is characterized by extensive RNA processing, including RNA editing. In chloroplasts of angiosperms, RNA editing proceeds by C-to-U base conversions at specific sites, while in chloroplasts of hornworts, many bryophytes and ferns, U-to-C conversions take place as well [1–3]. RNA editing events almost exclusively change codon identities, and usually restore codons conserved during land plant evolution. Mutational analyses of edited codons have demonstrated that editing is essential for protein function in vivo [4, 5]. The corresponding machinery is nuclear encoded, and recognizes short stretches of sequence immediately upstream of the C to be converted .
RNA editing has been found in chloroplasts of all major land plants. To date, there is no evidence for RNA editing in cyanobacteria, the closest prokaryotic relatives of chloroplasts, or in chlorophyte algae, the closest aquatic relatives of land plants. This phylogenetic distribution suggests that chloroplast RNA editing was "invented" close to the root of land plant radiation . Within land plants, the number of chloroplast RNA editing sites per genome differs among species. Bryophytes and ferns may possess several hundred C-to-U as well as U-to-C RNA editing sites [1–3]. The chloroplast genomes of seed plants harbor far fewer (~30) editing sites, and their location varies even between closely related taxa . At least one land plant, the liverwort Marchantia polymorpha, apparently contains no RNA editing sites , suggesting that, in principle, RNA editing can become lost from a chloroplast genome. An important question is how the species-specific patterns of editing sites – the editotypes – of seed plant chloroplasts evolved. Differences in editotypes between even closely related species, such as Nicotiana sylvestris, Nicotiana tomentosiformis and other Solanacean relatives, point to a rapid evolution of editing sites [8, 9]. A comparison of editing sites between dicot and monocot organelles supports this notion, demonstrating that the speed of editing site evolution equals or exceeds that of third-codon positions . Analyses of selected transcripts from exemplary species over a wide range of land plants have led to similar conclusions [3, 11, 12].
While these analyses were meant to illuminate the evolution of editing sites, they do not necessarily shed any light on the evolution of the corresponding editing machinery. To date, the only genetically identified essential editing factors are required for editing specific sites and belong to a family of nuclear-encoded RNA binding proteins, the pentatricopeptide repeat proteins (PPR) [13–19]. Most PPR genes are conserved throughout angiosperm evolution  and, unlike editing sites, do not rapidly evolve. In fact, in at least five specific cases, specific nuclear activity is retained in a species despite the loss of the corresponding editing site [5, 21, 22]. If a site-recognition factor is conserved throughout evolution, this should be reflected in the conservation of the corresponding editing-site cis-element, an assumption that was supported by a recent analysis of the psbL start codon editing site in 28 species, and the ndhD start codon editing site in 21 species . In an attempt to understand editing-site evolution at a higher resolution, we took advantage of the thousands of sequences from previous phylogenetic studies that are available for the chloroplast reading frame of the matK protein. We analyzed (i) the evolutionary pattern of matK editing sites in angiosperm evolution; (ii) the conservation of editing activity in angiosperms; and (iii) the conservation of editing cis-elements throughout angiosperm phylogeny.
Intrageneric loss of matKediting sites in angiosperms
matK is a chloroplast gene located within the trnK intron that is believed to play a role in RNA splicing of tRNA-K [UUU, [23, 24]]. matK is an expressed gene , and in many monocots, matK transcripts are edited at a single site, termed matK-1 . We recently identified an additional editing site in Arabidopsis, referred to as matK-2, at nucleotide position 706 (codon 236) relative to the start codon . The corresponding editing event leads to a codon change from histidine (CAU) to tyrosine (UAU). Here, we found a third site, matK-3, located 70 nucleotides downstream of site 2 that leads to a serine (UCU) to phenylalanine (UUU) codon transition (codon 259, see below).
The rapidly evolving matK gene has been a favorite for determining phylogenetic relationships in angiosperms. As a consequence, several thousand matK entries covering the entire angiosperm phylogenetic tree have accumulated in Genbank. We obtained and aligned 1255 matK sequences from all major angiosperm groups as well as several gymnosperm species, focusing our analysis on determining whether a C or a T was present at these two newly identified editing sites. For phylogenetic analysis, we mapped our findings onto two phylogenetic trees, one for each editing site [, see Additional files 1 and 2]. The leaves of the tree represent genera, which can include several species. Because both trees consist predominately of C-containing genera, the most parsimonious assumption is that the common ancestors of all angiosperms had a C at the editing site. In contrast, the gymnosperm taxa analyzed have a T at matK-2 and an A at matK-3. Whether the site was lost in gymosperms or gained in angiosperms cannot be determined based on our data. We were unable to extend our alignment to more basal embryophyte groups, such as mosses and ferns, due to extreme sequence divergence. Taken together, these data suggest that the matK-2 and matK-3 editing sites were already present in the ancestor of all angiosperms.
Given that the editing sites are ancestral, we next asked how many times the sites have been lost during angiosperm evolution. We first sought situations in the tree that are indicative of C-to-T transitions within genera. In most cases, all species within a genus share the same editing site. For example, 24 species in the genus Ceanothus carry a C at matK-2 (see Additional file 3). However, in six of the 298 genera analyzed, there are species that possessed either a C or a T at matK-2, suggestive of a recent base transition. Similarly, seven of the genera analyzed include species with either a C or a T at matK-3. We call such taxa "mixed genera" (see Additional File 4 – Table S1). Rarely, we also found mixed genera with A- or G-containing species in addition to T- or C-containing species (see Additional File 5 – Table S2). All mixed genera are nested in branches heavily dominated by pure C-containing genera (e.g., see Additional file 3), suggesting that C-losses occurred independently within these genera.
Frequent and widespread loss of editing sites within larger angiosperm taxa
If intrageneric loss of editing does occur, it should be also evident on a larger scale. We therefore assessed the distribution of pre-edited (T at the DNA-level) branches of the angiosperm phylogenetic tree that are particularly rich in available matK sequences (i.e., Rosids, Saxifragales, Asterids, Caryophyllids, Magnoliids and basal eudicots). Coherent sections of genera without an editing site, for example the Solanaceae/Convolvulaceae, were treated as a unit. We asked whether such pre-edited units are separated from other such units, which would suggest that they had lost editing independently. Only pre-edited units for which sister groups at the next three nodes in the tree contained equal or more than 80% of genera with a C at the editing site were regarded as having independently lost the editing site (see Additional file 3). A- and G-containing genera were not considered. By these criteria, we found evidence for 12 independent losses of edited Cs for matK-2 and another 12 for matK-3; these were widely distributed throughout the angiosperm tree (see Figure 1 and see Additional file 4 – Table S1). If the intrageneric losses noted above are included here, the number of independent losses for matK-2 and matK-3 rise to 17 and 19, respectively (Figure 1). Only the asterid genera Gilia and Plantago have lost both matK sites, underscoring that editing-site loss – even that of physically linked sites – is totally independent (Figure 1).
We found no evidence for reversion (i.e. T-to-C back-mutations) for matK-2, even within the purely T-containing, large monocot branch. This might indicate the existence of a selective bias towards losing the editing site. It is clear, however, that there are multiple independent losses of the matK editing sites throughout angiosperm phylogeny.
Loss of C-to-U processing in independent branches of the angiosperm tree at matK-2 and matK-3
The presence of a C at a known editing site is considered good evidence for the presence of a corresponding editing activity. For example, editing events have been successfully predicted by extrapolation from known sites for Atropa belladonna and Pisum sativum [29, 30]. Here, we sequenced amplified cDNA from leaf tissue to investigate RNA editing of matK-2 and matK-3 in 17 and 14 different angiosperm species, respectively, from disparate sections of the angiosperm phylogenetic tree (see Additional file 6). All species chosen had a C at the matK-2 editing sites in the plastid genome. Unexpectedly, we found that matK-2 was processed in only seven species (41.2%). In six of these, a C-peak was evident side-by-side with the T-peak in electropherograms. Thus, only a fraction of all transcripts is processed. No editing was detected in RNA samples from the remaining ten species. The loss of editing activity for matK-3 was not quite as dramatic; but again, no evidence for editing could be found for two species, and most of the remaining species exhibited only partial editing (see Additional file 6). We call species with a C at the editing site but no detectable editing activity "non-editors", while species that process the C to a U are called "editors". We conclude that editing activities for the matK sites have most likely been lost in these species, although the possibility that editing does occur in different tissues under different conditions cannot be ruled out at the moment.
To understand the phylogenetic distribution of the underlying RNA editing activities, we mapped our results on a phylogenetic tree (Figure 2B). Editing activities are found at widely separated positions of this tree. For example, editors and non-editors for matK-2 are found both in the eurosids I and the eurosids II. Similarly, matK-2 editors and non-editors are also present side-by-side in lamiids and campanulids within the asterid clade. This situation is repeated for matK-3, where the two species that have lost editing activity are from separate larger taxa: Reseda from the rosids and Buddleja from the asterids. Taken together with the ancestral nature of the matK editing sites, noted above, these findings argue for multiple independent losses of the editing activities.
To investigate whether these losses are reflected in the corresponding cis-elements, we generated a consensus sequence for all plants capable of editing and compared it with sequences from the non-editing plants (Figure 2A). We found that almost all non-editors contain one or multiple deviations from the consensus sequence deduced from the set of editors, suggesting a correlation between the loss of the editing activity and the evolutionary degeneration of the cis-element.
Conservation of putative recognition elements for a matK-2 trans-acting factor
Editing sites are recognized by RNA binding proteins that bind sequence elements immediately upstream of the C-residue to be edited. As long as binding and editing processes continue to occur, selection is expected to act to preserve these cis-elements. By contrast, it is expected that the loss of editing would be accompanied by the loss of conservation of trans-acting factor binding-site sequences. To identify such sequence elements, we prepared separate alignments of sequences containing a C and those containing a T at the matK editing sites (henceforth called C-elements and T-elements, respectively). To avoid a bias toward species-rich genera, we randomly selected one sequence from each genus. The sequences were aligned and analysed using the WebLogo software  in order to visualize sequence conservation, and alignments were scored from position -30 to +10, where the editing site is +1. Figure 2C shows a comparison of the conservation of this sequence window between C- and T-containing matK-2 and matK-3 sites. The following three conservational classes for individual nucleotides can be distinguished:
(i) Nucleotide positions that are conserved in both C- and T-elements; for example, at positions -27 to -25, -6 to -4 and +8 to +10 relative to matK-2, and -17 to -15 upstream of matK-3. These include third-codon positions (e.g., matK-2 positions -25 and -4; matK-3 positions -14 and -20), for which other evolutionary constraints apart from coding must be responsible.
(ii) Nucleotide positions that are variable in both T- and C-elements, mostly third-codon positions (e.g., matK-2 positions -22, -19 and -16).
(iii) Nucleotide positions that are conserved only in editors. For matK-2, we found five highly conserved positions at -7, -17, -18, -24 and -30 of C-elements, whereas the corresponding positions in T-elements are much more variable. Conservation of the dominant base at these positions is 100% (-7, -17), 96% (-18), 93% (-24) and 88% (-30) in C-elements, but only 83% (-7), 55% (-17), 62% (-18, -24) and 45% (-30) in T-elements (see also arrows in Figure 2C). Notably, the highly conserved T at base -7 in C-elements is at a third-codon position. An analysis of a longer stretch of sequence upstream of the matK-2 editing site revealed that differential conservation terminates at position -30, and thus coincides with the location of the expected cis-element for editing (data not shown). For matK-3, such differential conservation between C-elements and T-elements is less pronounced, although differences exist at positions -4, -7, -8, -12, -24, -27 and -28.
These comparisons demonstrate that selected upstream bases and the C at the editing site have co-evolved. Furthermore, high conservation of several third-codon positions in both C- and T-elements suggests a selective force that is independent of both amino-acid coding and the editing site at these positions. Finally, a stronger conservation of bases in T-sites relative to C-sites was not observed for matK-2 or matK-3, supporting the conclusion that the observed conservation bias is functionally linked to the editing site.
Loss of matKediting sites in angiosperm evolution
It is impossible to clearly infer the loss or gain of an editing site by examining a limited set of sequences because any conclusion drawn ultimately relies on only one informative site: the editing site itself. Thus, an understanding of the evolutionary history of RNA editing sites requires an analysis of a large set of related sequences. We have therefore investigated the evolutionary behavior of two editing sites and their presumptive cis-elements in the matK gene, an approach that allows us to track the editing site throughout a continuum of related angiosperm sequences. Our results show that C dominates the phylogenetic trees for both matK-2 and matK-3 sites; thus, the most parsimonious explanation is that both editing sites were already present in the ancestor of all angiosperms. A closer analysis of the distribution of species and genera lacking a C at the editing sites suggests that the C at both matK sites was lost independently on multiple occasions. These data support earlier work suggesting that ancient angiosperms contained high numbers of editing sites that were lost independently in separate taxonomic branches during angiosperm evolution . Our results are also consistent with a study on the evolution of mitochondrial editing that described multiple independent losses of editing sites in selected monocot taxa . Importantly, these studies collectively explain the variability of editotypes among angiosperms species solely by invoking loss of editing sites, and do not require a presumption of balanced loss and gain of sites. Although preliminary, our results show no evidence for re-acquisition of matK editing sites, as exemplified for matK-2 in the purely T-carrying monocots. This suggests that at least these two sites, and by extrapolation, possibly all plastid-editing sites, are "on the way out".
Loss of matKediting activity in angiosperm evolution
An unexpected finding of this study is the loss or reduction in RNA editing in many species despite the presence of a C at the editing site. Reduced editing can either be caused by the degeneration of nuclear-encoded editing factors or plastidial cis-elements that direct the editing machinery. Based on the assumption that the matK editing activities are ancient (like the sites themselves; see above), we argue for multiple independent losses of editing at both sites during angiosperm evolution. Editing of matK-3 leads to a change in the codons that results in incorporation of very different amino acids: serine and phenylalanine. Given the nature of this difference, it is remarkable that Buddleja and Reseda tolerate the loss of this editing event. By contrast, the rather minor physico-chemical change provided by an H-to-Y amino acid transition mediated by matK-2 editing might be less critical for protein function. Among the codon transitions caused by chloroplast RNA editing, this codon transition is one of the rarest and therefore might not be as important for protein function as the much more frequent S-to-L or P-to-L transitions. The MatK protein may tolerate both amino acids, in which case the loss of RNA editing would have only limited consequences for protein function. If it is indeed selectively neutral, the frequent loss of C observed here might be specific for matK editing and thus not generalizable to truly essential RNA-editing sites. However, the fact that several independent C-to-T mutations, but no T-to-C back-mutations, are observed at both sites suggests that the edited amino acid is under positive selection. A reduction or a loss of editing could generate such a selective pressure for a C-to-T mutation and lead to the elimination of an editing site. Therefore, our results suggest that a decay in editing efficiency precedes the loss of editing sites, as proposed by Schields and Wolfe . Whether a degeneration of editing factors or their corresponding cis-elements is responsible for the reductions in editing efficiency observed here cannot be determined by our analyses because the reductions co-occur with mutations in cis-elements. Notably, chloroplast genomes display an enhanced genetic drift and accumulate mildly deleterious point mutations . MatK is one of the most rapidly diverging plastidial genes and exhibits a relatively high rate of degeneration . Therefore, we speculate that it is rather the degeneration of cis-elements that leads to the observed reduction in editing efficiencies, which in turn generates the selective pressure responsible for the frequent losses of editing sites by C-to-T mutations.
Cis-elements of matKediting sites are under multiple selective constraints
We have carried out a phylogenetic analysis of predicted matK-2 and matK-3 cis-elements in order to identify a putative conserved binding site for the corresponding (unknown) trans-acting factor(s). Many bases in these cis-elements are conserved in both C- and T-elements, mostly due to coding constraints, but several third-codon positions are also conserved. This could mean that selection is acting on all analyzed sequences, no matter which base is present at the editing site. If this selection is sufficiently stringent and acts on all bases, there should be no conservation bias towards C-elements. Irrespective of RNA editing function, a factor binding to this sequence, either on DNA or RNA, could provide such a selective force.
Our analysis uncovered five bases that are highly conserved in sequences containing the matK-2 editing site, but not in those lacking the site. A co-evolution of these bases with the editing site most likely reflects a function for these bases in editing-site processing or recognition. Such co-evolving nucleotides have recently been identified for two chloroplast editing sites, albeit in a much smaller taxon sampling . Intriguingly, in vitro studies have demonstrated that bases within such cis-elements have strikingly unequal impacts on RNA editing [35, 36]. For example, mutations of the -2 and -3 nucleotides of the psbE editing site led to a pronounced reduction in editing efficiency in vitro, while mutations at the adjacent -4/-5 and +2/+3 sites had only minor effects . Similar major effects of single bases on editing have also been observed in vivo . The position-specific inhibition of activity is not reflected in a similar inhibition of binding: all mutated versions of cis-elements appear to be equally good binding sites for (unknown) trans-acting factors . Thus, the bases co-conserved with the matK-2 editing site might be important for RNA editing activity, while their role in binding of trans-acting factors could be minor. In other words, the same RNA-binding protein that attaches to C-elements might also bind to T-elements. Such a factor could perform an additional function (or functions) unrelated to editing, and conserved bases could be important for such secondary function(s) of the editing factor. This would explain why bases are conserved at several third-codon positions in both C- and T-elements. Recently, PPR proteins have been identified as editing factors [13, 14]. Although these proteins are highly conserved between rice and Arabidopsis , their target Cs are not: only nine editing positions are conserved between rice  and Arabidopsis . For instance, the ndhD editing site, served by CRR21 in Arabidopsis, is lacking in rice; however, despite absence of the corresponding site, an orthologous protein can be readily identified (data not shown). The simplest explanation is that these factors may be involved in editing, but also serve additional, evolutionarily more stable functions. Our finding that many species carrying a C at the editing site lack editing activity might indicate that the corresponding factors have been lost. Such a loss-of-factor scenario would be consistent with several studies that demonstrated that transfer of editing sites from one species to another often leads to a failure to process the heterologous site, i.e. are indicative of a loss of the corresponding editing factor [4, 21, 40]. Three observations, however, speak against this simple loss-of-factor scenario: (i) several transferred sites are heterologously edited [21, 22]; (ii) PPRs, the bona fide editing factors, are conserved in angiosperms and are thus not reflective of editotype variability; (iii) our phylogenetic analysis uncovered sequence conservation in cis-elements at third-codon positions, not only in editors but also in non-editors and T-carriers. These considerations lead us to hypothesize that the factors are conserved and still bind cis-elements, but their editing activity is compromised because of mutations that disrupt protein structure/function or subtly alter RNA binding properties Determining whether known editing factors have additional functions and whether these functions are conserved in species that are devoid of the cognate editing site would be of great value in testing this hypothesis.
In this paper, we focused on the evolution of chloroplast editing sites in angiosperms. We demonstrate for the entire angiosperm radiation that editing sites have been lost multiple independent times. Our data also uncover a surprisingly frequent reduction or loss of the corresponding activity in selected taxa. Finally, this large-scale analysis helped to detect nucleotides with close co-evolutionary ties to the edited C. The additional finding that evolutionary conservation of third-codon positions can be detected even in the absence of an edited C supports the idea that interactions of trans-acting factors with sequence elements surrounding editing sites take also place for reasons other than RNA editing.
All leaf material was collected in the Botanical Garden of Marburg, Germany.
RNA preparation/RT-PCR analysis
RNA extraction was performed using the TRIzol Reagent according to the supplier's instructions, or by a cetyltrimethylammonium bromide (CTAB)-based method as described by Zeng and Yang . Five to eight micrograms RNA were treated with DNaseI (Roche, 40 u, 1 h, 37°C) to remove any DNA contamination. The RNA was then purified by two phenol/chloroform extractions, one chloroform extraction and an ethanol/salt precipitation step. cDNA sequences were amplified by PCR (Qiagen) after reverse transcription using the Omniscript RT-Kit (Qiagen) employing random hexamers, or the One-Step-RT-PCR Kit (Qiagen). An aliquot of RNA that was not reverse transcribed served as a control PCR template for DNA contamination. Total cellular DNA was extracted using a standard CTAB-based method.
The following oligonucleotides (5'>3') were used to amplify matK-2 and matK-3 sequences from DNA or cDNA: rctccttctttgcatttattgcg (matk.for.a), gctccttctttgcatttattgag (matk.for.b), gcctcttctttgcatttattgcg (matk.for.c), gcctcttctttgcatttattacg (matk.for.d), ccttcttctttacattttttacg, (matk.for.e), acctcttctttgcatttattaag (matk.for.f), catgaaaggatccttgaacaacc (matk.rev.z), catgaagagatcctcgaggaacc (matk.rev.y), agagaarggktctttgaaaagcc (matk.rev.x), awgaaaagkatctttgaaaaacc (matk.rev.w), catgaaaggatccttsaacaaca (matk.rev.v), tatgaaaggattcttgaacaaac (matk.rev.u) and cgcaaaaggatccttaagtaacc (matk.rev.t).
PCR products were purified using the NucleoSpin Extract II-Kit (Macherey and Nagel) and sequenced using DYEnamic ET chemistry (GE Healthcare) according to the supplier's instructions. The products of the sequencing reactions were analyzed on an ABI 377 automated sequencer (Applied Biosystems) according to the manufacturer's instructions.
A total of 1255 matK sequences covering 298 major angiosperm genera were obtained from GenBank. All genera represent leaves of phylogenetic trees constructed by Soltis et al. [, see Additional files 1 and 2]. Sequences were aligned by ClustalW using default parameters  resulting in an alignment of 3455 nt. A 201-bp sequence window comprising the editing sites matK-2 and matK-3 was extracted from this alignment for analysis.
Wolf PG, Rowe CA, Hasebe M: High levels of RNA editing in a vascular plant chloroplast genome: analysis of transcripts from the fern Adiantum capillus-veneris. Gene. 2004, 339: 89-97. 10.1016/j.gene.2004.06.018.
Kugita M, Yamamoto Y, Fujikawa T, Matsumoto T, Yoshinaga K: RNA editing in hornwort chloroplasts makes more than half the genes functional. Nucleic Acids Res. 2003, 31 (9): 2417-2423. 10.1093/nar/gkg327.
Freyer R, Kiefer-Meyer MC, Kossel H: Occurrence of plastid RNA editing in all major lineages of land plants. Proc Natl Acad Sci USA. 1997, 94 (12): 6285-6290. 10.1073/pnas.94.12.6285.
Bock R, Kossel H, Maliga P: Introduction of a heterologous editing site into the tobacco plastid genome: the lack of RNA editing leads to a mutant phenotype. Embo J. 1994, 13 (19): 4623-4628.
Schmitz-Linneweber C, Kushnir S, Babiychuk E, Poltnigg P, Herrmann RG, Maier RM: Pigment Deficiency in Nightshade/Tobacco Cybrids Is Caused by the Failure to Edit the Plastid ATPase alpha-Subunit mRNA. Plant Cell. 2005, 17: 1815-1828. 10.1105/tpc.105.032474.
Schmitz-Linneweber C, Barkan A: RNA splicing and RNA editing in chloroplasts. Cell and Molecular Biology of Plastids. Edited by: Bock R. 2007, Berlin, Heidelberg: Springer, 19: 213-248.
Maier RM, Neckermann K, Igloi GL, Kossel H: Complete sequence of the maize chloroplast genome: gene content, hotspots of divergence and fine tuning of genetic information by transcript editing. J Mol Biol. 1995, 251 (5): 614-628. 10.1006/jmbi.1995.0460.
Kahlau S, Aspinall S, Gray JC, Bock R: Sequence of the tomato chloroplast DNA and evolutionary comparison of solanaceous plastid genomes. J Mol Evol. 2006, 63 (2): 194-207. 10.1007/s00239-005-0254-5.
Sasaki T, Yukawa Y, Miyamoto T, Obokata J, Sugiura M: Identification of RNA Editing Sites in Chloroplast Transcripts from the Maternal and Paternal Progenitors of Tobacco (Nicotiana tabacum): Comparative Analysis Shows the Involvement of Distinct Trans-Factors for ndhB Editing. Mol Biol Evol. 2003, 20 (7): 1028-1035. 10.1093/molbev/msg098.
Shields DC, Wolfe KH: Accelerated evolution of sites undergoing mRNA editing in plant mitochondria and chloroplasts. Mol Biol Evol. 1997, 14 (3): 344-349.
Fiebig A, Stegemann S, Bock R: Rapid evolution of editing sites in a small non-essential plastid gene. Nucl Acids Res. 2004, 7: 3615-3622. 10.1093/nar/gkh695.
Hayes ML, Hanson MR: High Conservation of a 5' Element Required for RNA Editing of a C Target in Chloroplast psbE Transcripts. J Mol Evol. 2008, 67 (3): 233-245. 10.1007/s00239-008-9101-9.
Okuda K, Myouga F, Motohashi R, Shinozaki K, Shikanai T: Conserved domain structure of pentatricopeptide repeat proteins involved in chloroplast RNA editing. Proc Natl Acad Sci USA. 2007, 104 (19): 8178-8183. 10.1073/pnas.0700865104.
Kotera E, Tasaka M, Shikanai T: A pentatricopeptide repeat protein is essential for RNA editing in chloroplasts. Nature. 2005, 433 (7023): 326-330. 10.1038/nature03229.
Chateigner-Boutin AL, Ramos-Vega M, Guevara-Garcia A, Andres C, de la Luz Gutierrez-Nava M, Cantero A, Delannoy E, Jimenez LF, Lurin C, Small I, et al: CLB19, a pentatricopeptide repeat protein required for editing of rpoA and clpP chloroplast transcripts. Plant J. 2008, 56 (4): 590-602. 10.1111/j.1365-313X.2008.03634.x.
Zehrmann A, Verbitskiy D, Merwe van der JA, Brennicke A, Takenaka M: A DYW Domain-Containing Pentatricopeptide Repeat Protein Is Required for RNA Editing at Multiple Sites in Mitochondria of Arabidopsis thaliana. Plant Cell. 2009, 21 (2): 558-567. 10.1105/tpc.108.064535.
Robbins JC, Heller WP, Hanson MR: A comparative genomics approach identifies a PPR-DYW protein that is essential for C-to-U editing of the Arabidopsis chloroplast accD transcript. RNA. 2009, 15 (6): 1142-1153. 10.1261/rna.1533909.
Cai W, Ji D, Peng L, Guo J, Ma J, Zou M, Lu C, Zhang L: LPA66 Is Required for Editing psbF Chloroplast Transcripts in Arabidopsis. Plant Physiol. 2009, 150: 1260-1271. 10.1104/pp.109.136812.
Zhou W, Cheng Y, Yap A, Chateigner-Boutin AL, Delannoy E, Hammani K, Small I, Huang J: The Arabidopsis gene YS1 encoding a DYW protein is required for editing of rpoB transcripts and the rapid development of chloroplasts during early growth. Plant J. 2009, 58: 82-96. 10.1111/j.1365-313X.2008.03766.x.
O'Toole N, Hattori M, Andres C, Iida K, Lurin C, Schmitz-Linneweber C, Sugita M, Small I: On the expansion of the pentatricopeptide repeat gene family in plants. Mol Biol Evol. 2008, 25 (6): 1120-1128. 10.1093/molbev/msn057.
Tillich M, Poltnigg P, Kushnir S, Schmitz-Linneweber C: Maintenance of plastid RNA editing activities independently of their target sites. EMBO Rep. 2006, 7: 308-313. 10.1038/sj.embor.7400619.
Karcher D, Kahlau S, Bock R: Faithful editing of a tomato-specific mRNA editing site in transgenic tobacco chloroplasts. RNA. 2008, 14 (2): 217-224. 10.1261/rna.823508.
Neuhaus H, Link G: The chloroplast tRNA(Lys) (UUU) gene from mustard (Sinapis alba) contains a class II intron potentially encoding for a maturase-related polypeptide. Curr Genet. 1987, 11: 251-257. 10.1007/BF00355398.
Ems SC, Morden CW, Dixon CK, Wolfe KH, dePamphilis CW, Palmer JD: Transcription, splicing and editing of plastid RNAs in the nonphotosynthetic plant Epifagus virginiana. Plant Mol Biol. 1995, 29 (4): 721-733. 10.1007/BF00041163.
Barthet MM, Hilu KW: Expression of matK: functional and evolutionary implications. Am J Bot. 2007, 94: 1402-1412. 10.3732/ajb.94.8.1402.
Tillich M, Schmitz-Linneweber C, Herrmann RG, Maier RM: The plastid chromosome of maize (Zea mais): Update of the complete sequence and transcript editing sites. Maize Genet Corp News Letters. 2001, 75: 42-44.
Tillich M, Funk HT, Schmitz-Linneweber C, Poltnigg P, Sabater B, Martin M, Maier RM: Editing of plastid RNA in Arabidopsis thaliana ecotypes. Plant J. 2005, 43 (5): 708-715. 10.1111/j.1365-313X.2005.02484.x.
Soltis DE, Soltis PS, Chase MW, Mort ME, Aalbach DC, Zanis M, Savolainen V, Hahn WH, Hoot SB, Fay MF, et al: Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences. Bot J Lin Soc. 2000, 133: 381-461.
Schmitz-Linneweber C, Regel R, Du TG, Hupfer H, Herrmann RG, Maier RM: The plastid chromosome of Atropa belladonna and its comparison with that of Nicotiana tabacum: the role of RNA editing in generating divergence in the process of plant speciation. Mol Biol Evol. 2002, 19 (9): 1602-1612.
Inada M, Sasaki T, Yukawa M, Tsudzuki T, Sugiura M: A systematic search for RNA editing sites in pea chloroplasts: an editing event causes diversification from the evolutionarily conserved amino acid sequence. Plant Cell Physiol. 2004, 45 (11): 1615-1622. 10.1093/pcp/pch191.
Crooks GE, Hon G, Chandonia JM, Brenner SE: WebLogo: a sequence logo generator. Genome Res. 2004, 14 (6): 1188-1190. 10.1101/gr.849004.
Tillich M, Lehwark P, Morton BR, Maier UG: The evolution of chloroplast RNA editing. Mol Biol Evol. 2006, 23 (10): 1912-1921. 10.1093/molbev/msl054.
Lopez L, Picardi E, Quagliariello C: RNA editing has been lost in the mitochondrial cox3 and rps13 mRNAs in Asparagales. Biochimie. 2007, 89 (1): 159-167. 10.1016/j.biochi.2006.09.011.
Lynch M, Blanchard JL: Deleterious mutation accumulation in organelle genomes. Genetica. 1998, 102–103 (1–6): 29-39. 10.1023/A:1017022522486.
Miyamoto T, Obokata J, Sugiura M: A site-specific factor interacts directly with its cognate RNA editing site in chloroplast transcripts. Proc Natl Acad Sci USA. 2004, 101 (1): 48-52. 10.1073/pnas.0307163101.
Heller WP, Hayes ML, Hanson MR: Cross-competition in editing of chloroplast RNA transcripts in vitro implicates sharing of trans-factors between different C targets. J Biol Chem. 2008, 283 (12): 7314-7319. 10.1074/jbc.M709595200.
Reed ML, Peeters NM, Hanson MR: A single alteration 20 nt 5' to an editing target inhibits chloroplast RNA editing in vivo. Nucleic Acids Res. 2001, 29 (7): 1507-1513. 10.1093/nar/29.7.1507.
Corneille S, Lutz K, Maliga P: Conservation of RNA editing between rice and maize plastids: are most editing events dispensable?. Mol Gen Genet. 2000, 264 (4): 419-424. 10.1007/s004380000295.
Chateigner-Boutin AL, Small I: A rapid high-throughput method for the detection and quantification of RNA editing based on high-resolution melting of amplicons. Nucleic Acids Res. 2007, 35 (17): e114-10.1093/nar/gkm640.
Reed ML, Hanson MR: A heterologous maize rpoB editing site is recognized by transgenic tobacco chloroplasts. Mol Cell Biol. 1997, 17 (12): 6948-6952.
Zeng Y, Yang T: RNA isolation from highly viscous samples rich in polyphenols and polysaccharides. Plant Mol Biol Rep. 2002, 20: 417a-417e. 10.1007/BF02772130.
Thompson J, Higgins D, Gibson T: Clustal W: Improving the sensitivity of progressive multiple sequnce alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucl Acids Res. 1994, 22: 4673-4680. 10.1093/nar/22.22.4673.
We thank students who participated in the Cell-Biology class of 2005 at the University of Marburg for their help in analyzing the editing status of matK in several angiosperm species, and Helena T. Funk and Peter Poltnigg, who tutored the course together with MT. Special thanks to Marc Appelhans for his guidance through the botanical garden of Marburg. This work was supported by the Deutsche Forschungsgemeinschaft (SFB-TR1 to UGM, Emmy-Noether stipend to CSL); AvH also thankfully acknowledges financial support from the Vienna Science and Technology Fund (WWTF).
MT conceived of the study, carried out the cDNA analyses together with KS and participated in the sequence alignment. VLS and AvH generated the sequence alignment and mapped the results for matK editing sites on the phylogenetic tree. CSL participated in the design of the study and wrote the draft manuscript. All authors contributed to writing the manuscript and drawing the figures, and all approved the final version.
Electronic supplementary material
Additional file 1: matK -2 editing sites in angiosperms. This phylogenetic tree shows all detected losses for matK editing site 2 during angiosperm evolution. (PDF 40 KB)
Additional file 2: matK -3 editing sites in angiosperms. This phylogenetic tree shows all detected losses for matK editing site 3 during angiosperm evolution. (PDF 39 KB)
Additional file 3: matK -2 editing sites lost during Angiosperm evolution. An excerpt of the phylogenetic tree shown in Additional file 1 labeled to demonstrate the method used to evaluate losses of editing sites during matK evolution in angiosperms. (PDF 25 KB)
Additional file 6: Analysis of matK-2 and matK-3 editing in selected species. Excerpts from cDNA sequencing electropherograms are shown to demonstrate the extent of editing in selected angiosperm species. (PDF 354 KB)
About this article
Cite this article
Tillich, M., Le Sy, V., Schulerowitz, K. et al. Loss of matKRNA editing in seed plant chloroplasts. BMC Evol Biol 9, 201 (2009). https://doi.org/10.1186/1471-2148-9-201
- Editing Site
- Editing Event
- Editing Activity
- Editing Efficiency
- Angiosperm Evolution