- Research article
- Open Access
The physical and functional borders of transit peptide-like sequences in secondary endosymbionts
© Felsner et al; licensee BioMed Central Ltd. 2010
- Received: 2 December 2009
- Accepted: 19 October 2010
- Published: 19 October 2010
Plastids rely on protein supply by their host cells. In plastids surrounded by two membranes (primary plastids) targeting of these proteins is facilitated by an N-terminal targeting signal, the transit peptide. In secondary plastids (surrounded by three or four membranes), transit peptide-like regions are an essential part of a bipartite topogenic signal sequence (BTS), and generally found adjacent to a N-terminally located signal peptide of the plastid pre-proteins. As in primary plastids, for which no wealth of functional information about transit peptide features exists, the transit peptide-like regions used for import into secondary ones show some common features only, which are also poorly characterized.
We modified the BTS (in the transit peptide-like region) of the plastid precursor fucoxanthin-chlorophyll a/c binding protein D (FcpD) fused to GFP as model substrate for the characterization of pre-protein import into the secondary plastids of diatoms. Thereby we show that (i) pre-protein import is highly charge dependent. Positive net charge is necessary for transport across the plastid envelope, but not across the periplastid membrane. Acidic net charge perturbs pre-protein import within the ER. Moreover, we show that (ii) the mature domain of the pre-protein can provide intrinsic transit peptide functions.
Our results indicate important characteristics of targeting signals of proteins imported into secondary plastids surrounded by four membranes. In addition, we show a self-targeting mechanism, in which the mature protein domain contributes to the transit peptide function. Thus, this phenomenon lowers the demand for pre-sequences evolved during the course of endosymbiosis.
- Mature Protein
- Transit Peptide
- Envelope Membrane
- Apicomplexan Parasite
- Mature Domain
Primary plastids are organelles of endosymbiontic origin [e.g. 1, 2]. In the course of the transition from an (endo-)symbiont to an organelle, most of its genes were either lost or, to a higher degree, transferred into the cell nucleus [e.g. 3, 4, 5]. Hence, most of the plastid proteome is encoded in the nucleus of the host cell, implying that the encoded proteins must be transported post-translationally across the two envelope membranes into the plastid lumen. For accurate trafficking, nearly all nuclear-encoded plastid proteins are equipped with a characteristic N-terminal topogenic signal sequence, the transit peptide . This targeting information is necessary and sufficient for plastid import and interacts with translocons of the outer/inner envelope membrane of chloroplasts [TOC and TIC; recently reviewed in 7]. Interestingly, surveys of transit peptides indicate no strict consensus sequence  but some common features such as a positive net charge, elevated levels of hydroxylated amino acids and binding motifs for molecular chaperones [9 and references therein].
Secondarily evolved organisms such as diatoms, apicomplexa or cryptophytes harbour plastids surrounded by two additional membranes [10, 11]. Genomic analyzes indicated a common set of nuclear-encoded proteins with a plastid destination as in primary plastids . In contrast to the primary plastids, proteins here are equipped with a bipartite topogenic signal sequence (BTS), consisting of a classical ER-like signal peptide (SP) followed by a transit peptide-like sequence (TP) [2, 12, 13]. This transit peptide-like sequence is - as in archaeplastida - indispensable for plastid import as shown by in vivo experiments on apicomplexa and diatoms [5, 14, 15]. Recently, Tonkin et al.  demonstrated that even randomly picked sequences, which follow the basic rules for transit peptides (see above), could function as targeting sequences in apicomplexa, indicating a low complexity of transit peptides. However, in diatoms and cryptophytes, at least one major difference to the apicomplexan transit peptide composition exists, which is the presence of a highly conserved aromatic amino acid at position +1 of the TP crucial for plastid protein import [5, 15, 17]. The TPs of apicomplexa are not as heavily dependent on the phenylalanine as diatoms and cryptophytes .
Protein import is charge-dependent
Because transit peptides of land plants possess a positive net charge crucial for proper import into chloroplasts , we first tested the localization of GFP fused to the BTS of the fucoxanthin-chlorophyll a/c binding protein D (FcpD) of the diatom Phaeodactylum tricornutum with respect to the transit peptide (TP) charge. We chose FcpD (NCBI accession number Z24768) as our model precursor, since its 24 amino acids (aa) long BTS displays all features of a typical diatom plastid pre-protein [e.g. ref. 19 and references therein]. The signal peptide (M1-A15) of the BTS is predicted by SignalP to be cleaved after position 15, giving way to the typically short transit peptide-like region  with the conserved phenylalanine (F16) at +1. The transit peptide (9 aa long (F16-R24, predicted by ChloroP) is as expected enriched in hydroxylated aa and alanine, and contains two positively charged residues, K20 and R24. Acidic residues are absent. We draw the line between BTS and mature domain of the protein between aa N30 and M31, since the conserved region of the chlorophyll a-b binding protein domain starts at F33. Hence, we replaced the M31 and the following aa of the mature domain with our reporter - eGFP - turning aa N30 to T.
Constructs investigated in this study
... FAPA K NAA R TSVATT-MVS K ...
... FAPA K NAA R TSVATT-MVS E ...
... FAPA K NAA R TSVATT-MVS A ...
... FAPA E NAA E TSVATT-MVS E ...
... FAPA R NAA R TSVATT-MVS R ...
... FAPA A NAA A TSVATT-MVS A ...
... FAPA E NAA E TSVATT-MVS K ...
... FAPA EK AA E TSVATT-MVS K ...
... FAPA EK AA E TSVATT-MVS E ...
... FAPA A NAA A TSVATT-MVS K ...
... FAPA ER AA E TSVATT-MVS R ...
... FAPA ER AA E TSVATT-MVS E ...
... FAPA-MVS K ...
... FAPA-MVS R ...
... FAPA-MVS E ...
... FAPA-MVS A ...
... FAPA K NAA R TSVATT-[M(GGGGP) 5 ] 3 -MVS K ...
... FAPA-[M(GGGGP) 5 ]-MVS K ...
... FAPA-[m(GGGGP) 5 ] 2 -MVS K ...
... FAPA-[M(GGGGP) 5 ] 3 -MVS K ...
... FAPA-[M(GG K GP)-(GGGGP) 4 ] 3 -MVS K ...
The mature protein can possess transit peptide function
The enslavement and reduction of once free-living cyanobacteria and phototrophic protists to what we today refer to as primary or secondary plastids was accompanied by subsequent cellular and genomic reductions. The plastid genome shrunk enormously by massive gene transfers [and by gene losses; e.g. 23] to the host nucleus. Nonetheless, most of the gene products are still required to maintain plastid function so that the bulk of proteins must be re-imported into the plastid post-translationally. Hence, the development of efficient import machineries for pre-proteins destined for the various sub-compartments of the plastid was doubtlessly indispensable in plastid evolution. Pre-protein import into primary plastids is mediated by an N-terminal targeting signal, the transit peptide . Extensive analyzes of various plant transit peptides reported only some "weak" common features like e.g. a positive net charge , which was shown to be essential to successfully cross the plastid envelope. Such features were detected in bioinformatic investigations of transit peptide-like sequences of secondary plastid-bearing organisms as well . To date, protein import into complex plastids can be studied in vivo by light-microscopic approaches using fluorescently labelled proteins. However, the exact interpretation of the obtained results is often insufficient because of the resolution limits of microscopes. For instance, evaluation of successful pre-protein import into the four-membrane-bound plastid (apicoplast) of apicomplexan parasites such as Plasmodium falciparum is always an all-or-none decision, as one cannot distinguish between the sub-apicoplast compartments. In contrast, the cell size of the diatom P. tricornutum gives rise to the advantage that not only import into the plastid stroma can be investigated, but also transport across only some of the four surrounding envelope membranes can be tracked [5, 15, 17]. Thus, application of P. tricornutum as a model system for studying pre-protein import into secondary plastids makes such studies more precise.
Like in land plant plastids, transit peptide-like function in P. tricornutum relies on the presence of basic/positively charged aa residues [24, 25]. This holds true for the BTS of the FcpD precursor fused to GFP as well. Moreover, pivotal for proper transit peptide function is not the particular moiety, but solely the positive charge present (Figure 2c, e, f). In particular, substitution of the charged residues to alanines reveals that, as a first approximation (charge dependent PPM translocation will be discussed below), protein import across the PPM might not be charge dependent, but is across the plastid envelope (cf. Figure 2a and 2d). In addition, the substitution of the basic residues with acidic/negatively charged aa totally impedes import into the stroma (as seen by the ER-localization of the GFP in Figure 2b). A high load of N-terminally located negative charges might be a mechanism to prevent ER-resident proteins from being accidentally PPC-targeted. For example, the ER-residential Hsp70 chaperone BiP and the ER-residential ER quality control protein Calreticulin exhibit four acidic charges in the first six and eleven amino acids, respectively, at the N-terminus of the mature protein.
Secondary plastids of diatoms are surrounded by four membranes. The outermost of these is surmounted by pre-proteins using the SP of the BTS to enter the chloroplast ER lumen . From then on, the TP mediates the passage across the sequent membranes. The lack of a functional TP leads to an arrest of the pre-protein within the ER or the PPC in the diatom (as seen above) and even to its secretion in apicomplexan parasites [24, 25], in which the secondary symbiont does not directly reside within a perinuclear ER cisterna [a detailed description of plastid morphology is given in 1]. Hence, the transit peptide facilitates the passage of the pre-protein across the former symbiontic plasma membrane (the periplastid membrane, PPM) before the pre-proteins gain access to the genuine (primary) plastid envelope. The TP of the FcpD BTS, in which the positively charged residues are substituted with glutamate (K20E, R24E see Figure 3 and Table 1), suffices for at least a partial import of GFP into the PPC (Figure 3a, d). Here, the transit peptide net charge is negative (-2 or -1 when K4 of GFP is included). Therefore, the generic plant-like transit peptide characteristics seem to be less important for the passage across the PPM than for the passage across the plastid envelope. We mentioned above that transport across the PPM can take place in a charge independent manner, but as seen in Figure 3a and 3e positive charges can outweigh negative ones. The fact that GFP is only partially imported might be caused by the order and number of the charged aa within the TP. Here, the first two negative charges may somehow shield the basic residue of the GFP and interfere with the translocon in the PPM. This is consistent with the results obtained with a construct, in which an additional lysine (N21K) was introduced between the negatively charged TP (Figure 3b). Here, the GFP was entirely imported into the PPC. However, by fusing this TP to the GFP, in which K4 was substituted with a glutamate (Figure 3c), GFP fluorescence was obtained exclusively in the ER. From these results, the following two essential consequences can be deduced: (i) An impact of the reporter GFP on pre-protein import as already shown in Figure 3a becomes evident and (ii) import across the PPM can depend on discrete positively charged residues rather than on a global basic net charge of the TP, but not in either case (see Figure 2d). Notably, Tonkin et al. reported that positive aa in the N-termini of apicoplast TPs are essential for proper apicoplast import as well . But due to the different morphology of the apicoplast, pre-protein import is already halted at the stage of apicoplast targeting/recognition.
As outlined before, the TP of the FcpD BTS is compared to plant TP relatively short, and an influence of the mature part of FcpD on pre-protein import was taken into account. To investigate this in more detail, we trimmed the TP such that the four remaining residues of the transit peptide lack any charge. According to our and previous data [outlined in 9], the TP should have been dysfunctional but it was not (Figure 4a). Contrarily, the truncated TP fused to the K4E GFP stopped protein import from proceeding beyond the ER. Interestingly, the construct comprising the shortened TP and the K4A_GFP led to a localization within the periplastidal compartment (Figure 4c). This means that the residual TP aa, which can be hardly termed TP-like anymore, mediates translocation of a further membrane. This result suggests that the TP is not required for the transport across the PPM. As a consequence, one would no longer consider the acquisition of the BTS - and therefore of a TP - of PPC-targeted proteins as critical step for proper targeting. Quite the opposite, it seems that non aromatic or to some level acidic aa within the TP have to be present, to prevent aberrant (stromal) targeting. At present, we cannot define, whether the information for the PPM passage resides within the remainder of the TP (the sequence FAPA) or within the GFP (or a combination of both).
To demonstrate the influence of the GFP lysine in more detail, we introduced a spacer peptide between the truncated TP and wild type GFP (see Figure 4d,e; Table 1). These experiments clearly indicate the assistance of the reporter on pre-protein translocation across the PPM. Surprisingly, only a threefold repeat was able to impede GFP import (Figure 4d). While this manuscript was in revision, Bionda and coworkers published that the critical length requirement of TPs of plant primary plastids is about 60 aa . This is in line with our observations, since a twofold and threefold spacer repeats add up to 52 and 78 aa, respectively. After introducing a lysine into the spacer GFP import was at least partially re-established (Figure 4e). Consistently, the reporter - or to generalize - the mature domain can influence its transport by contributing essential aa for TP functionality. The poor efficiency of stromal import obtained in these experiments is most likely due to the composition of the spacer, whose sequence does not resemble the classical make-up of TPs commonly present in diatoms [15, 19]. At the moment, we cannot exactly specify the distance that can be bypassed by positive charges to act on TPs for proper targeting. In the spacer constructs, as mentioned above, a twofold repetition of the synthetic spacer, which totals 52 amino acids, did not block plastid import (Figure 4d). On the other hand, wild type GFP cannot drive plastid import when fused to a neutralized TP (K20A, R24A, see Figure 3d). Supposably, the environment of the charged residue affects the contribution to the targeting process. In any case, these results contradict previous attempts to define the minimal unit of the TP that is indispensable for accurate protein targeting [15, 27] and indicate that the physical and functional borders of a TP are not necessarily identical. This means that the acquired N-terminal extension during endosymbiosis, the physical TP, does not contain always all features that are essential for targeting, the functional TP. We have therefore shown that the characteristics of topogenic signals required for pre-protein import into secondary plastids, as inferred from previous studies , must be supplemented by our data on TP positive charge presented here. Anyhow, the observed discrepancy of the functional/physical TP border to the mature protein hampers the prediction of (peri-)plastid-directed proteins, as these are commonly identified by characteristics of "self-sufficient" transit peptides, meaning those which contain all topogenic information necessary for import. Potential plastid pre-proteins therefore, if preceded by a rather short BTS or SP only, should be re-examined and the N-terminal portion of the mature domain has to be taken into account, while predicting a (sub-)cellular localization of a protein. On the other hand the in vivo localization of a putative plastid protein by genetically fusing a potential BTS to GFP might be misleading.
Since organellar genes have been transferred to the nuclear genome in secondarily evolved organisms, the acquisition of appropriate targeting signals was a key issue for their accurate re-direction to the plastid sub-compartments. As even random sequences that match only the elementary characteristics of TPs, serve as functional pre-sequences , the complexity of a genuine TP seems to be rather low. Therefore the constraints for a DNA sequence to act as a functional transit peptide is diminished to the most basic features. Hence, if (plastid) proteins - as exemplified above - possess intrinsic information for their own (sub-)organellar targeting spontaneous self-targeting might be an evolutionary driving force that facilitated and/or accelerated the successful integration of the transferred genetic material in to the new genetic background. Thus, transit peptides may evolve by exon shuffling from pre-existing plastid-targeted genes [6, 16, 21] and/or by the help of the here demonstrated self-targeting mechanism, by which the transit peptides are moulded from the N-terminal part of the mature protein by subsequent mutation.
In summary, our results offered new insights into the features of pre-protein targeting signals in secondary plastids. Beyond its requirement for crossing the plastid envelope, discrete positive aa residues can play a role in the import across the PPM. Common transit peptide features are not essential for this import step. In addition, we demonstrated that the mature domain of the protein (here the GFP reporter) facilitated its own translocation, consequently reducing the degree of topogenic capacity necessary in the signal preceding the mature protein. This self-targeting in turn might have enhanced the successful expression of plastid genes targeted to the nucleus during evolution.
Lastly, our results presumably can be generalized for the other plastid-harbouring organisms as well, since (i) many factors of the translocation machineries are conserved in archaeplastida [28, 29], (ii) some of them, as well as the putative import machinery embedded in the PPM, are present in complex plastids and the apicoplast, respectively [30–33], and (iii) transit peptides are cross-species functional [e.g. 20, 34, 35, 36, 37].
eGFP and eYFP constructs were generated with terminal 5' EcoRI and 3' HindIII restriction sites. The presequences were linked via NcoI sites to GFP and YFP, respectively. DNA fragments were amplified using the PHUSION High-Fidelity DNA polymerase (Finnzymes, Espoo, Finland) or Biotools DNA polymerase (Madrid, Spain). Amino acid substitutions were carried out by PCR-based mutagenesis using primers with respective sequences (see Additional file 1). Presequences and the GFP/YFP-encoding fragment were ligated into the transformation vector pPhaT1 in one step. Prior to the integration of the spacer sequences (provided by GeneArt, Regensburg, Germany), the respective construct was temporarily integrated into pBluescript II KS+. Linearization by restriction with NcoI and dephosphorylation of DNA termini by shrimp alkaline phosphatase preceded the addition of the spacers. The small fragment (GFP11) of the self assembly GFP system  was introduced 5' via the first AluI restriction site of eGFP and 3' via HindIII. The plasmid used for this system, the induction procedure and the analysis are described elsewhere . For cotransfection the ble gene of the plasmid pPhaT1 was substituted for the nat1 gene (provided by WERNER BioAgents, Jena, Germany) conferring resistance to nourseothricin. All constructs were checked for fidelity as well as number and orientation of integrated spacers by sequencing.
Cell culture, transformation and in vivo localization
Cultivation and biolisitc transformation of Phaeodactylum tricornutum was carried out according to Apt et al. 1996 . Cotransfected cells were selected on plates containing 75 μg/ml nourseothricin (WERNER BioAgents, Jena, Germany). Analysis of recombinant cells was performed with a Leica TCS SP2 confocal laser-scanning microscope using the settings as described  for the GFP and chlorophyll fluorescence. YFP images were obtained by excitation of the chromophore at 514 nm and the usage of a DD 458/514 beam splitter.
We thank Geoff Waldo (Los Alamos, USA) for providing the self-assembly GFP technology and Andrew Bozarth (Marburg) for comments on the manuscript. This work was funded by the Deutsche Forschungsgemeinschaft (Collaborative Research Centre 593).
- Cavalier-Smith T: Genomic reduction and evolution of novel genetic membranes and protein-targeting machinery in eukaryote-eukaryote chimaeras (meta-algae). Philos Trans R Soc Lond B Biol Sci. 2003, 358 (1429): 109-133. 10.1098/rstb.2002.1194. discussion 133-104PubMedPubMed CentralView ArticleGoogle Scholar
- Bolte K, Bullmann L, Hempel F, Bozarth A, Zauner S, Maier UG: Protein targeting into secondary plastids. J Eukaryot Microbiol. 2009, 56 (1): 9-15. 10.1111/j.1550-7408.2008.00370.x.PubMedView ArticleGoogle Scholar
- Martin W, Stoebe B, Goremykin V, Hapsmann S, Hasegawa M, Kowallik KV: Gene transfer to the nucleus and the evolution of chloroplasts. Nature. 1998, 393 (6681): 162-165. 10.1038/30234.PubMedView ArticleGoogle Scholar
- Martin W, Rujan T, Richly E, Hansen A, Cornelsen S, Lins T, Leister D, Stoebe B, Hasegawa M, Penny D: Evolutionary analysis of Arabidopsis, cyanobacterial, and chloroplast genomes reveals plastid phylogeny and thousands of cyanobacterial genes in the nucleus. Proc Natl Acad Sci USA. 2002, 99 (19): 12246-12251. 10.1073/pnas.182432999.PubMedPubMed CentralView ArticleGoogle Scholar
- Gruber A, Vugrinec S, Hempel F, Gould SB, Maier UG, Kroth PG: Protein targeting into complex diatom plastids: functional characterisation of a specific targeting motif. Plant Mol Biol. 2007, 64 (5): 519-530. 10.1007/s11103-007-9171-x.PubMedView ArticleGoogle Scholar
- Bruce BD: Chloroplast transit peptides: structure, function and evolution. Trends Cell Biol. 2000, 10 (10): 440-447. 10.1016/S0962-8924(00)01833-X.PubMedView ArticleGoogle Scholar
- Jarvis P: Targeting of nucleus-encoded proteins to chloroplasts in plants. New Phytol. 2008, 179 (2): 257-285. 10.1111/j.1469-8137.2008.02452.x.PubMedView ArticleGoogle Scholar
- Bruce BD: The paradox of plastid transit peptides: conservation of function despite divergence in primary structure. Biochim Biophys Acta. 2001, 1541 (1-2): 2-21. 10.1016/S0167-4889(01)00149-5.PubMedView ArticleGoogle Scholar
- Soll J, Schleiff E: Protein import into chloroplasts. Nat Rev Mol Cell Biol. 2004, 5 (3): 198-208. 10.1038/nrm1333.PubMedView ArticleGoogle Scholar
- Archibald JM: The puzzle of plastid evolution. Curr Biol. 2009, 19 (2): R81-88. 10.1016/j.cub.2008.11.067.PubMedView ArticleGoogle Scholar
- Keeling PJ: Chromalveolates and the evolution of plastids by secondary endosymbiosis. J Eukaryot Microbiol. 2009, 56 (1): 1-8. 10.1111/j.1550-7408.2008.00371.x.PubMedView ArticleGoogle Scholar
- Hempel F, Bozarth A, Sommer MS, Zauner S, Przyborski JM, Maier UG: Transport of nuclear-encoded proteins into secondarily evolved plastids. Biol Chem. 2007, 388 (9): 899-906. 10.1515/BC.2007.119.PubMedView ArticleGoogle Scholar
- Gould SB, Waller RF, McFadden GI: Plastid evolution. Annu Rev Plant Biol. 2008, 59: 491-517. 10.1146/annurev.arplant.59.032607.092915.PubMedView ArticleGoogle Scholar
- Waller RF, Reed MB, Cowman AF, McFadden GI: Protein trafficking to the plastid of Plasmodium falciparum is via the secretory pathway. Embo J. 2000, 19 (8): 1794-1802. 10.1093/emboj/19.8.1794.PubMedPubMed CentralView ArticleGoogle Scholar
- Kilian O, Kroth PG: Identification and characterization of a new conserved motif within the presequence of proteins targeted into complex diatom plastids. Plant J. 2005, 41 (2): 175-183. 10.1111/j.1365-313X.2004.02294.x.PubMedView ArticleGoogle Scholar
- Tonkin CJ, Foth BJ, Ralph SA, Struck N, Cowman AF, McFadden GI: Evolution of malaria parasite plastid targeting sequences. Proc Natl Acad Sci USA. 2008, 105 (12): 4781-4785. 10.1073/pnas.0707827105.PubMedPubMed CentralView ArticleGoogle Scholar
- Gould SB, Sommer MS, Hadfi K, Zauner S, Kroth PG, Maier UG: Protein targeting into the complex plastid of cryptophytes. J Mol Evol. 2006, 62 (6): 674-681. 10.1007/s00239-005-0099-y.PubMedView ArticleGoogle Scholar
- Ralph SA, Foth BJ, Hall N, McFadden GI: Evolutionary pressures on apicoplast transit peptides. Mol Biol Evol. 2004, 21 (12): 2183-2194. 10.1093/molbev/msh233.PubMedView ArticleGoogle Scholar
- Patron NJ, Waller RF: Transit peptide diversity and divergence: A global analysis of plastid targeting signals. Bioessays. 2007, 29 (10): 1048-1058. 10.1002/bies.20638.PubMedView ArticleGoogle Scholar
- Gould SB, Sommer MS, Kroth PG, Gile GH, Keeling PJ, Maier UG: Nucleus-to-Nucleus Gene Transfer and Protein Retargeting into a Remnant Cytoplasm of Cryptophytes and Diatoms. Mol Biol Evol. 2006, 23 (12): 2413-2422. 10.1093/molbev/msl113.PubMedView ArticleGoogle Scholar
- Kilian O, Kroth PG: Presequence acquisition during secondary endocytobiosis and the possible role of introns. J Mol Evol. 2004, 58 (6): 712-721. 10.1007/s00239-004-2593-z.PubMedView ArticleGoogle Scholar
- Cabantous S, Terwilliger TC, Waldo GS: Protein tagging and detection with engineered self-assembling fragments of green fluorescent protein. Nat Biotechnol. 2005, 23 (1): 102-107. 10.1038/nbt1044.PubMedView ArticleGoogle Scholar
- Timmis JN, Ayliffe MA, Huang CY, Martin W: Endosymbiotic gene transfer: organelle genomes forge eukaryotic chromosomes. Nat Rev Genet. 2004, 5 (2): 123-135. 10.1038/nrg1271.PubMedView ArticleGoogle Scholar
- Foth BJ, Ralph SA, Tonkin CJ, Struck NS, Fraunholz M, Roos DS, Cowman AF, McFadden GI: Dissecting apicoplast targeting in the malaria parasite Plasmodium falciparum. Science. 2003, 299 (5607): 705-708. 10.1126/science.1078599.PubMedView ArticleGoogle Scholar
- Tonkin CJ, Roos DS, McFadden GI: N-terminal positively charged amino acids, but not their exact position, are important for apicoplast transit peptide fidelity in Toxoplasma gondii. Mol Biochem Parasitol. 2006, 150 (2): 192-200. 10.1016/j.molbiopara.2006.08.001.PubMedView ArticleGoogle Scholar
- Bionda T, Tillmann B, Simm S, Beilstein K, Ruprecht M, Schleiff E: Chloroplast Import Signals: The Length Requirement for Translocation In Vitro and In Vivo. J Mol Biol. 2010, 402 (3): 510-523. 10.1016/j.jmb.2010.07.052.PubMedView ArticleGoogle Scholar
- Apt KE, Zaslavkaia L, Lippmeier JC, Lang M, Kilian O, Wetherbee R, Grossman AR, Kroth PG: In vivo characterization of diatom multipartite plastid targeting signals. J Cell Sci. 2002, 115 (Pt 21): 4061-4069. 10.1242/jcs.00092.PubMedView ArticleGoogle Scholar
- Kalanon M, McFadden GI: The chloroplast protein translocation complexes of Chlamydomonas reinhardtii: a bioinformatic comparison of Toc and Tic components in plants, green algae and red algae. Genetics. 2008, 179 (1): 95-112. 10.1534/genetics.107.085704.PubMedPubMed CentralView ArticleGoogle Scholar
- Steiner JM, Yusa F, Pompe JA, Loffelhardt W: Homologous protein import machineries in chloroplasts and cyanelles. Plant J. 2005, 44 (4): 646-652. 10.1111/j.1365-313X.2005.02559.x.PubMedView ArticleGoogle Scholar
- McFadden GI, van Dooren GG: Evolution: red algal genome affirms a common origin of all plastids. Curr Biol. 2004, 14 (13): R514-516. 10.1016/j.cub.2004.06.041.PubMedView ArticleGoogle Scholar
- Sommer MS, Gould SB, Lehmann P, Gruber A, Przyborski JM, Maier UG: Der1-mediated pre-protein import into the periplastid compartment of chromalveolates?. Mol Biol Evol. 2007, 24 (3): 1-11.Google Scholar
- van Dooren GG, Tomova C, Agrawal S, Humbel BM, Striepen B: Toxoplasma gondii Tic20 is essential for apicoplast protein import. Proc Natl Acad Sci USA. 2008, 105 (36): 13574-13579. 10.1073/pnas.0803862105.PubMedPubMed CentralView ArticleGoogle Scholar
- Agrawal S, van Dooren GG, Beatty WL, Striepen B: Genetic evidence that an endosymbiont-derived ERAD system functions in import of apicoplast proteins. J Biol Chem. 2009, 284 (48): 33683-33691. 10.1074/jbc.M109.044024.PubMedPubMed CentralView ArticleGoogle Scholar
- DeRocher A, Hagen CB, Froehlich JE, Feagin JE, Parsons M: Analysis of targeting sequences demonstrates that trafficking to the Toxoplasma gondii plastid branches off the secretory system. J Cell Sci. 2000, 113 (Pt 22): 3969-3977.PubMedGoogle Scholar
- Lang M, Apt KE, Kroth PG: Protein transport into "complex" diatom plastids utilizes two different targeting signals. J Biol Chem. 1998, 273 (47): 30973-30978. 10.1074/jbc.273.47.30973.PubMedView ArticleGoogle Scholar
- Nassoury N, Cappadocia M, Morse D: Plastid ultrastructure defines the protein import pathway in dinoflagellates. J Cell Sci. 2003, 116 (Pt 14): 2867-2874. 10.1242/jcs.00517.PubMedView ArticleGoogle Scholar
- Wastl J, Maier UG: Transport of proteins into cryptomonads complex plastids. J Biol Chem. 2000, 275 (30): 23194-23198. 10.1074/jbc.M003125200.PubMedView ArticleGoogle Scholar
- Hempel F, Bullmann L, Lau J, Zauner S, Maier UG: ERAD-derived pre-protein transport across the second outermost plastid membrane of diatoms. Mol Biol Evol. 2009, 26 (8): 1781-1790. 10.1093/molbev/msp079.PubMedView ArticleGoogle Scholar
- Apt KE, Kroth-Pancic PG, Grossman AR: Stable nuclear transformation of the diatom Phaeodactylum tricornutum. Mol Gen Genet. 1996, 252 (5): 572-579.PubMedGoogle Scholar
- Kalanon M, Tonkin CJ, McFadden GI: Characterization of two putative protein translocation components in the apicoplast of Plasmodium falciparum. Eukaryot Cell. 2009, 8 (8): 1146-1154. 10.1128/EC.00061-09.PubMedPubMed CentralView ArticleGoogle Scholar
- Spork S, Hiss JA, Mandel K, Sommer M, Kooij TW, Chu T, Schneider G, Maier UG, Przyborski JM: An unusual ERAD-like complex is targeted to the apicoplast of Plasmodium falciparum. Eukaryot Cell. 2009, 8 (8): 1134-1145. 10.1128/EC.00083-09.PubMedPubMed CentralView ArticleGoogle Scholar
- Bullmann L, Haarmann R, Mirus O, Bredemeier R, Hempel F, Maier UG, Schleiff E: Filling the gap, evolutionarily conserved Omp85 in plastids of chromalveolates. J Biol Chem. 285 (9): 6848-6856. 10.1074/jbc.M109.074807.Google Scholar
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