Notice: Wiley Online Library will be unavailable on Saturday 27th February from 09:00-14:00 GMT / 04:00-09:00 EST / 17:00-22:00 SGT for essential maintenance. Apologies for the inconvenience.
Angiosperm plastid genomes typically encode approximately 80 polypeptides, mainly specifying plastid-localized functions such as photosynthesis and gene expression. Plastid protein synthesis and expression of the plastid clpP1 gene are essential for development in tobacco, indicating the presence of one or more plastid genes whose influence extends beyond the plastid compartment. The plastid accD gene encodes the β-carboxyl transferase subunit of acetyl-CoA carboxylase and is present in the plastids of most flowering plants, including non-photosynthetic parasitic plants. We replaced the wild-type accD gene with an aadA-disrupted mutant allele using homologous recombination. Persistent heteroplasmy in the presence of antibiotics indicated that the wild-type accD allele was essential. The phenotype of the accD knockout was revealed in plastid transformants grown in the absence of antibiotics. Leaves contained pale green sectors and lacked part or all of the leaf lamina due to arrested division or loss of cells. Abnormal structures were present in plastids found in mutant plants, indicating that accD might be required to maintain the plastid compartment. Loss of the plastid compartment would be expected to be lethal. These results provide genetic evidence showing the essential role of plastid ACCase in the pathway leading to the synthesis of products required for the extra-plastidic processes needed for leaf development.
If you can't find a tool you're looking for, please click the link at the top of the page to "Go to old article view". Alternatively, view our Knowledge Base articles for additional help. Your feedback is important to us, so please let us know if you have comments or ideas for improvement.
Plastids contain their own genetic system which, in most flowering plants, codes for around 110 different genes (Wakasugi et al., 2001). The majority of plastid genes code for photosynthesis-related proteins, or protein and RNA components of the plastid expression apparatus (Wakasugi et al., 2001). Plastid transformation is well established in tobacco, enabling reverse-genetic approaches to be used to study the functions of plastid genes. Knockouts of 21 plastid genes encoding polypeptides have revealed loss-of-function phenotypes that specifically affect plastids (Maliga, 2004). Mutants deficient in photosynthesis-related functions grow and develop on media containing sucrose. In addition to genes with plastid-limited functions, the observations that inhibition of plastid protein synthesis arrests development of tobacco seedlings (Zubko and Day, 1998) and leaves (Ahlert et al., 2003) suggest that the expression of one or more plastid genes is required for plant development.
The tobacco plastid genome is known to encode a number of essential genes including ycf1, ycf2 (Drescher et al., 2000) and clpP1 (Shikanai et al., 2001). Knockouts of these genes result in persistent heteroplasmy where both wild-type (WT) and aadA disrupted-mutant alleles are required for survival on selection media containing antibiotics (Drescher et al., 2000; Shikanai et al., 2001). The regulatory clpP1 gene is required for tobacco development (Kuroda and Maliga, 2003) and encodes a subunit of a protease which must act on essential plastid polypeptide(s), but these might be encoded by nuclear or plastid genes. Plastid protein synthesis is dispensable in cereals (Hess et al., 1993; Walbot and Coe, 1979; Zubko and Day, 2002) and Brassica napus (Zubko and Day, 1998), demonstrating the absence of essential plastid-encoded proteins in these species. In cereals and B. napus, genes located in the nucleus could encode plastid-targeted proteins that replace the functions of the essential plastid genes present in tobacco. Tobacco plastid genes that are absent in cereal plastid genomes are candidates for essential tobacco genes. The clpP1 gene is present in cereal plastid DNA, but the list of absent genes in cereal plastid genomes includes ycf1, ycf2 and accD (Wakasugi et al., 2001). Both clpP and accD genes are transcribed by a nucleus-encoded plastid RNA polymerase, which acts early in development (Hajdukiewicz et al., 1997; Hanaoka et al., 2005; Liere et al., 2004). The accD, ycf1 and ycf2 genes are present in the minimal plastid genome of the non-photosynthetic holoparasite Epifagus virginiana (Wolfe et al., 1992), indicating their importance.
To inactivate accD, we removed 198 bp of accD coding sequences and 473 bp of upstream DNA in plastid transformation vector pUM86 (Figure 1a). This removes bases 59 320–59 990 of the 155 939-bp tobacco plastid genome (Wakasugi et al., 1998). The pUM75 control vector (Figure 1b) contains an intact accD gene. Both transformation vectors contain aadA marker gene- and uidA reporter gene-expression cassettes (Iamtham and Day, 2000; Zubko et al., 2004). The plastid DNA sequences flanking the foreign genes target integration by homologous recombination, allowing the isolation of antibiotic-resistant plastid transformants. Plastid genomes are present in multiple copies per cell. Following transformation, transgenic plastid genomes represent a small fraction of the WT plastid genomes in a cell. Transgenic plastids are selected with antibiotics until they replace all WT plastids, resulting in homoplasmic plants containing only transgenic plastid genomes. All 18 independently isolated pUM75 plastid transformants were homoplasmic and were indistinguishable in appearance from green WT plants (Figure 2c).
Four pUM86 transformants (clones 4, 5, 8 and 10), which contain a deleted accD gene, were isolated from independent transformation events. The leaves of all four pUM86 ΔaccD transformants were variegated with white sectors (Figure 2a) resulting from spectinomycin-induced bleaching. Both the first T0 and second T1 generations (Figure 2j) exhibited this phenotype on spectinomycin medium. When white leaf areas were regenerated into plants on antibiotic-free media, only green shoots resembling WT shoots were isolated (not shown). On transfer of variegated plants to antibiotic-free medium, the new upper leaves lacked white sectors (Figure 2b).
Analysis of ΔaccD plastid transformants
Green–white (GW) variegation indicates a heteroplasmic mixture of transgenic and WT plastid genomes. This was confirmed by DNA blot analysis. Hybridization with left and right plastid (pt) DNA probes (Figure 1c) detected transgenic 13.6-kb SacI and 3.9-kb HindIII bands, and WT 10.6-kb SacI and 11.5-kb HindIII bands in digests of variegated GW leaf DNA from pUM86 ΔaccD plants grown on spectinomycin medium (Figure 3a, lanes 4 and 6). In contrast, control pUM75 transformants, with an intact accD gene, lacked WT plastid DNA and gave rise to predominant 14.3-kb SacI and 4.6-kb HindIII transgenic bands in DNA digests (Figure 3a, lane 2). A 3.7-kb HindIII band in digests probed with aadA confirmed the presence of foreign genes in pUM75 and pUM86 plants (Figure 3a, lanes 2–6) and their absence in WT plants (Figure 3a, lane 1). Persistent heteroplasmy in the presence of antibiotics indicates that both WT and aadA-disrupted accD alleles are required for viability, and is indicative of a knockout in an essential plastid gene (Drescher et al., 2000; Fischer et al., 1996; Shikanai et al., 2001).
Leaf-loss phenotype of ΔaccD plants grown in the absence of antibiotics
The phenotype of the accD knockout was revealed when plants were grown in the absence of antibiotics. New leaves exhibited a striking pattern of pale green sectors and lacked large sections of the leaf lamina (Figure 2d–i). In some cases, one (Figure 2g,h) or both halves of the leaf lamina (Figure 2i) were missing. This leaf-loss phenotype in the absence of antibiotics has not been reported previously with knockouts in 28 plastid genes (Maliga, 2004). In tobacco, removal of spectinomycin normally results in regreening of new, correctly shaped leaves (Iamtham and Day, 2000; Zubko and Day, 1998). Pale green sectors and leaf lamina loss were visible in new leaves long after withdrawal of antibiotics, and are unlikely to represent any residual effects of antibiotics. Pale green sectors and leaf lamina loss were visible in new leaves of one ΔaccD clone right up to flowering. Seeds collected following selfing of this plant gave rise to 39 variegated spectinomycin-resistant seedlings (Figure 2j) among 439 progeny seedlings. The inheritance of ΔaccD transgenic plastid genomes further confirms their persistence in soil-grown plants.
DNA blot analysis of leaf areas containing pale green sectors from ΔaccD plants grown in the absence of antibiotics revealed the presence of both transgenic and WT plastid genomes using the right and left plastid DNA probes (Figure 1c). Transgenic 13.6-kb SacI and 3.9-kb HindIII bands, and WT 10.6-kb SacI and 11.5-kb HindIII bands were detected in digests of DNA from variegated green/pale green leaves from pUM86 ΔaccD plants (Figure 3a, lanes 3 and 5) grown in the absence of antibiotics. PCR analysis was used to study plastid genomes in pale green leaf sectors from soil-grown plants (Figure 2d–f) and white leaf sectors from plants grown on spectinomycin (Figure 2a). DNA extracts (Klimyuk et al., 1993) from small leaf pieces were taken to minimize contamination of sectors with green cells. Transgenic ΔaccD plastid genomes were detected in white and pale green leaf sectors with primers uidA-R and pt-R, which amplified a 0.8-kb product spanning the accD deletion from pUM86 ΔaccD plant extracts and a larger 1.5-kb PCR product from pUM75 control plants (Figure 3b, upper panel). When primer pt-F was added, an additional 1.5-kb WT plastid band was amplified from all white and pale green sectors in pUM86 ΔaccD plants (Figure 3b, lower panel). We were unable to detect leaf explants with only ΔaccD mutant genomes by DNA blot and PCR analysis.
Microscopic analysis of pale green sectors in ΔaccD plants
Light microscopic examination of transverse leaf sections revealed a narrowing of the leaf lamina in pale green sectors. Wild-type leaves contain an upper epidermis, palisade mesophyll, spongy mesophyll and lower epidermis (Figure 4a). In pale green leaf sectors a clear palisade layer, which requires functional plastids for its development (Keddie et al., 1996; Pyke et al., 2000), was not visible in the mesophyll (Figure 4b). Epidermal cells and mesophyll cells were irregular in shape and had a flattened appearance in pale green sectors (Figure 4b). Sections spanning the transition across a sector from normal green to pale green revealed a thinning of the leaf lamina (Figure 4c). The transition was gradual in comparison with the sharp sector boundaries found in leaves where cells with fully functional chloroplasts lie adjacent to cells with debilitated plastids (Pyke et al., 2000). This is consistent with sectoring in pUM86 leaves resulting from a progressive decrease in functional plastids from green to pale green areas. Unlike normal green leaves, where chloroplasts are the most abundant plastid type (Figure 4d), pale green sectors contained a variety of plastid forms. A feature of chloroplasts in mutant leaves was the presence of unusual aberrant structures that disrupted the outer regions of chloroplasts (Figure 4e), which were not found in chloroplasts in WT plants (Figure 4d). Vesicle-like structures were found within the stroma of chloroplasts from mutant leaves (Figure 4e): these resemble vesicles found in chloroplasts in senescent leaves (Chory et al., 1991).
Replacement of the WT accD gene with an aadA disrupted-mutant allele resulted in persistent heteroplasmy, despite strong selection pressure with two antibiotics and multiple rounds of regeneration. Heteroplasmic ΔaccD plants exhibited a leaf-loss phenotype and contained pale green sectors when grown either in vitro or in soil in the absence of antibiotics. A control construct containing an intact accD gene gave rise to homoplasmic plastid transformants with a uniform population of transgenic plastid genomes and normal leaves. Other insertions in the rbcL-accD intergenic region (Iamtham and Day, 2000; Svab and Maliga, 1993; Zubko et al., 2004) including our pUM75 control plants; or an insert just upstream of the psaI coding region (Zhang et al., 2001) and knockouts of the rbcL (Kanevski and Maliga, 1994), ycf10 (Swiatek et al., 2003) and petA (Klaus et al., 2003; Monde et al., 2000) genes, that leave the accD gene intact, have also led to the isolation of homoplasmic tobacco plants. A knockout of a ycf4 homologue in Chlamydomonas reinhardtii gave rise to homoplasmic mutant algae unable to accumulate the photosystem I complex (Boudreau et al., 1997). Inactivation of the psaI gene of Synechocystis led to a small defect in photosystem I function, which did not affect photoautotrophic growth at 25°C (Xu et al., 1995). These results indicate that the rbcL, psaI, ycf4, ycf10 and petA genes flanking accD are dispensable. Heteroplasmy in pUM86 ΔaccD plants is specific to the deletion in accD and appears unlikely to result from any long-range effect of the ΔaccD deletion on neighbouring genes.
Persistent heteroplasmy under selection is characteristic of an aadA disruption in an essential plastid gene. In a unicellular organism such as C. reinhardtii, homoplasmy of a mutant essential gene is cell- and organism-lethal (Fischer et al., 1996). In a multicellular tobacco plant, homoplasmy of a mutant essential gene within a fraction of cells would be lethal to these cells, but the plant would survive provided there are sufficient viable heteroplasmic cells present. Homoplasmic cells would result from segregation of WT and ΔaccD plastid genomes during the cell divisions accompanying growth and development. Cells containing a homoplasmic population of mutant accD plastid genomes would not be viable, resulting in a loss of leaf cells. This absence of leaf cells would indicate that accD is an essential gene. Consistent with this idea, we were unable to detect homoplasmic mutant leaf sections. Homoplasmy of the ΔaccD mutation resulting in a deficiency of plastidic malonyl CoA might be expected to lead to cell loss in a number of organs. The observation that the phenotype was most noticeable in leaves is probably because loss of leaf lamina in a fraction of leaves is not lethal to the plant. Loss of cells in other organs might account for the observations that ΔaccD plants grow more slowly than WT plants, and some mutant plants had weak, twisted stems.
The multicopy state of plastid DNA enables visualization of the phenotype of an essential gene at different developmental stages. The variation in sector sizes and positions, and irregular pattern of leaf lamina loss in pUM86 ΔaccD plants, is consistent with random segregation of mutant and WT plastid genomes. The variable pattern of leaf lamina loss suggests that accD is required at all stages of leaf development. In contrast, a homozygous plant for an essential nuclear gene would arrest at the first developmental stage at which its product was needed (Baud et al., 2003). This is also true of a Cre-LoxP method that excises all copies of the essential clpP1 plastid gene simultaneously resulting in early arrest of shoot development (Kuroda and Maliga, 2003).
Variation in leaf thickness, and a variety of plastid developmental forms resulting from different mutant-to-WT accD allele ratios, probably underlie the pale green sectors found in our ΔaccD knockout plants. A striking feature of plastids in mutant leaves was the presence of unusual aberrant structures that disrupted the outer regions of chloroplasts. These lesions might be explained by the idea that a reduction in malonyl CoA levels could lead to an accumulation of 8-, 10- and 12-carbon fatty acids, which have detergent-like properties resulting in membrane distortion and eventual plastid lysis (Bungard, 2004). Reduced malonyl CoA levels within plastids would result from depletion of plastid-localized ACCase due to inactivation of accD. Plastids are widely considered to house essential metabolic pathways, and disruption of the compartment, which provides the correct environment for their functionality, might be expected to be lethal.
Evolution of plastids from endosymbiotic bacteria involved gene transfer to the nucleus and plastid genome compaction. The essential role of accD shows that plastids have not relinquished complete control of leaf development to the nucleus. The presence of accD in plastids enables gene expression in light-harvesting organelles to influence the development of leaves, which are the light-harvesting organs of plants. The accD gene is also present in the plastids of non-photosynthetic plants (Bungard, 2004; Wolfe et al., 1992). In an extension of the redox control hypothesis (Pfannschmidt et al., 1999) to explain the selective retention of plastid genes, the presence of accD in plastids rather than the nucleus would allow each plastid to influence ACCase activity according to its needs (Bungard, 2004). Our work suggests that accD is an influential gene required to maintain plastid structure, which is consistent with a requirement for regulating its expression in individual plastids.
The presence of essential plastid-encoded proteins in tobacco plastids contrasts with the dispensability of plastid protein synthesis in cereals and Brassica species. These contradictory findings in different species require an explanation. Cereal plastids lack the plastid accD gene (Wakasugi et al., 2001) and eubacterial-type multisubunit ACCase (Konishi and Sasaki, 1994; Sasaki and Nagano, 2004), but contain a eukaryotic-type ACCase comprised of multimers of a single multifunctional polypeptide, which is encoded by the nucleus (Gornicki et al., 1997; Sasaki and Nagano, 2004). Brassica napus does contain a eubacterial-type multisubunit plastid ACCase (Elborough et al., 1996), but also contains a second eukaryotic-type ACCase in plastids, which is encoded by the nucleus (Schulte et al., 1997). These alternative nucleus-encoded plastid ACCases would allow plastids lacking ribosomes to synthesize malonyl CoA. This idea suggests that the presence of a functional plastid ACCase is the only requirement for the dispensability of protein synthesis in plastids. It would predict the apparent absence or limited expression of a nuclear-coded eukaryotic-type ACCase in tobacco plastids, and identifies accD as an essential plastid gene. Our results are also consistent with the suggestion that the plastid envelope is impermeable to malonyl-CoA (Harwood, 1991; Sasaki and Nagano, 2004) because malonyl-CoA cannot be supplied to plastids from the cytosol to rescue the ΔaccD mutation. The indispensability of multisubunit ACCase in tobacco has provided us with genetic evidence to demonstrate the importance of plastid ACCase for maintaining plastid structure and the development of leaves.
Expression cassettes contained the aadA gene (Goldschmidt-Clermont, 1991) flanked by the 16S rrnBn promoter/rbcL ribosome-binding site (EMBL accession no. AJ276677) (Iamtham and Day, 2000) and BnpsbC 3′ UTR (EMBL accession no. AJ578474) (Zubko et al., 2004), and uidA gene flanked by 16S rrnHv promoter/rbcL ribosome-binding site (EMBL accession no. AJ276676) and NtpsbA 3′ UTR (Iamtham and Day, 2000). A linker with ApaI and NotI sites was inserted into the AocI site of pTB27 to make pTB27-link (Zubko et al., 2004). The aadA and uidA expression cassettes were excised from Bluescript vectors (Short et al., 1988) with ApaI and NotI, and inserted into the ApaI site of pTB27-link to construct pUM75. The accD deletion in pUM86 was made by replacing the NotI to XhoI fragment in pTB27-link (removes bases 59320–60493) with a HinfI to XhoI fragment (bases 59 991–60 493). The NotI and HinfI ends were treated with Klenow enzyme and nucleoside triphosphates to allow blunt-end ligation. The deletion was confirmed by sequencing. The aadA and uidA expression cassettes were then inserted into the ApaI site of the deleted pTB27-link vector to make pUM86.
Isolation of transplastomic plants
Plastid transformants were generated by particle bombardment as described (Day et al., 2004; Svab and Maliga, 1993) using Nicotiana tabacum (cv. Wisconsin 38). Green shoots and cell lines were selected on RMOP medium (Svab and Maliga, 1993) containing spectinomycin dihydrochloride pentahydrate plus streptomycin sulphate, each at 500 mg l−1. After three cycles of regeneration on RMOP media containing spectinomycin and streptomycin, shoots were rooted on Murashige and Skoog (MS) medium containing 200 mg l−1 spectinomycin. Plants with roots were propagated in vitro in the presence or absence of spectinomycin, or transferred to soil. The clone number identifies the bombardment from which it was obtained. Plants in vitro were propagated in a growth cabinet at 25°C in a 12-h day/12-h night cycle with light intensities of 40–100 μE m−2 sec−1. Plants in soil were grown in a walk-in growth room at 25°C in a 16-h day/8-h night cycle with light intensities of 80–200 μE m−2 sec−1. Seeds from self-pollinated ΔaccD plants were germinated on MS medium containing 80 or 100 mg l−1 spectinomycin.
Total DNA extractions and DNA blot analyses were carried out as described (Zubko and Day, 2002). [α-32P]dCTP hybridization probes prepared with High Prime (Roche Applied Science, Lewes, UK) were comprised of a 0.8-kbp NcoI–PstI aadA fragment from pUC-atpX (Goldschmidt-Clermont, 1991), the left 1.4-kbp probe (co-ordinates 57 595–59 028) containing the rbcL gene prepared from pTB27 using primers rbcl-F (5′-ATGTCACCACAAACAGAGACTA) and rbcl-R (5′-TTACTTATCCAAAACGTCCACT), and the right 0.74-kbp probe (co-ordinates 59 793–60 533) containing the accD gene prepared from pTB27 with primers accD-F (5′- ATGACTATTCATCTATTGTATTTTC) and pt-R (5′-GCATTGAACCCACAAATGCCTG). Blots were washed in 0.1 × saline sodium citrate, 0.1% (w/v) sodium dodecyl sulphate at 60°C. DNA extracts from small samples of tissue were prepared according to Klimyuk et al. (1993) for PCR analysis. Aliquots of 1 μl DNA extract were used in a final volume of 25 μl 1 × ReadyMix Taq with MgCl2 (Sigma-Aldrich, Poole, UK). PCR utilized primers pt-F (5′-GCAGTGGACGTTTTGGATAAG, 59 005–59 025), pt-R (60 512–60 553) and uidA-R (5′-CACAGTTTTCGCGATCCAGACTGAATG-3′) using 25 cycles of 95°C for 25 sec, 58°C for 45 sec and 72°C for 2 min.
Microscopy was carried out as described by Zubko and Day (1998). Leaf pieces (1–2 mm) were fixed in 2.5% glutaraldehyde in 0.1 m sodium cacodylate pH 7.3, post-fixed in cacodylate buffer containing 0.01 mg ml−1 osmium tetroxide, dehydrated in an ethanol series and embedded in Spurr's resin. Sections were stained in 1% toluidene blue for light microscopy and 2% uranyl acetate, 0.3% lead citrate for transmission electron microscopy using a Phillips/FEI Tecnai 12 Biotwin transmission electron microscope (FEI Company, Eindhoven, The Netherlands).
Supported by Overseas Research Students awards to V. Kode and S. Iamtham, University Research Studentship award to V. Kode, and Royal Thai Government Scholarship to S. Iamtham. A.D. was supported by the Biotechnology and Biological Sciences Research Council. We thank Dr J. Whatley (Oxford) for advice on plastid ultrastructure, and the EM facility for assistance.