Role of Aminoalcoholphosphotransferases 1 and 2 in Phospholipid Homeostasis in Arabidopsis

Aminoalcoholphosphotransferase (AAPT) catalyzes the synthesis of phosphatidylcholine (PC) and phosphotidylethanolamine (PE), which are the most prevalent membrane phospholipids in all eukaryotic cells. Here, we show that suppression of AAPTs results in extensive membrane phospholipid remodeling in Arabidopsis thaliana. Double knockout (KO) mutants that are hemizygous for either aapt1 or aapt2 display impaired pollen and seed development, leading to embryotic lethality of the double KO plants, whereas aapt1 or aapt2 single KO plants show no overt phenotypic alterations. The growth rate and seed yield of AAPT RNA interference (RNAi) plants are greatly reduced. Lipid profiling shows decreased total galactolipid and phospholipid content in aapt1-containing mutants, including aapt1, aapt1/aapt1 aapt2/AAPT2, aapt1/AAPT1 aapt2/aapt2, and AAPT RNAi plants. The level of PC in leaves was unchanged, whereas that of PE was reduced in all AAPT-deficient plants, except aapt2 KO. However, the acyl species of PC was altered, with increased levels of C34 species and decreased C36 species. Conversely, the levels of PE and phosphatidylinositol were decreased in C34 species. In seeds, all AAPT-deficient plants, including aapt2 KO, displayed a decrease in PE. The data show that AAPT1 and AAPT2 are essential to plant vegetative growth and reproduction and have overlapping functions but that AAPT1 contributes more than AAPT2 to PC production in vegetative tissues. The opposite changes in molecular species between PC and PE and unchanged PC level indicate the existence of additional pathways that maintain homeostatic levels of PC, which are crucial for the survival and proper development of plants.     

Brassinosteroid Regulates Cell Elongation by Modulating Gibberellin Metabolism in Rice

Brassinosteroid (BR) and gibberellin (GA) are two predominant hormones regulating plant cell elongation. A defect in either of these leads to reduced plant growth and dwarfism. However, their relationship remains unknown in rice (Oryza sativa). Here, we demonstrated that BR regulates cell elongation by modulating GA metabolism in rice. Under physiological conditions, BR promotes GA accumulation by regulating the expression of GA metabolic genes to stimulate cell elongation. BR greatly induces the expression of D18/GA3ox-2, one of the GA biosynthetic genes, leading to increased GA₁ levels, the bioactive GA in rice seedlings. Consequently, both d18 and loss-of-function GA-signaling mutants have decreased BR sensitivity. When excessive active BR is applied, the hormone mostly induces GA inactivation through upregulation of the GA inactivation gene GA2ox-3 and also represses BR biosynthesis, resulting in decreased hormone levels and growth inhibition. As a feedback mechanism, GA extensively inhibits BR biosynthesis and the BR response. GA treatment decreases the enlarged leaf angles in plants with enhanced BR biosynthesis or signaling. Our results revealed a previously unknown mechanism underlying BR and GA crosstalk depending on tissues and hormone levels, which greatly advances our understanding of hormone actions in crop plants and appears much different from that in Arabidopsis thaliana.     

The Arabidopsis Malectin-Like Leucine-Rich Repeat Receptor-Like Kinase IOS1 Associates with the Pattern Recognition Receptors FLS2 and EFR and Is Critical for Priming of Pattern-Triggered Immunity

Plasma membrane-localized pattern recognition receptors such as FLAGELLIN SENSING2 (FLS2) and EF-TU RECEPTOR (EFR) recognize microbe-associated molecular patterns (MAMPs) to activate the first layer of plant immunity termed pattern-triggered immunity (PTI). A reverse genetics approach with genes responsive to the priming agent β-aminobutyric acid (BABA) revealed IMPAIRED OOMYCETE SUSCEPTIBILITY1 (IOS1) as a critical PTI player. Arabidopsis thaliana ios1 mutants were hypersusceptible to Pseudomonas syringae bacteria. Accordingly, ios1 mutants demonstrated defective PTI responses, notably delayed upregulation of PTI marker genes, lower callose deposition, and mitogen-activated protein kinase activities upon bacterial infection or MAMP treatment. Moreover, Arabidopsis lines overexpressing IOS1 were more resistant to P. syringae and demonstrated a primed PTI response. In vitro pull-down, bimolecular fluorescence complementation, coimmunoprecipitation, and mass spectrometry analyses supported the existence of complexes between the membrane-localized IOS1 and FLS2 and EFR. IOS1 also associated with BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1) in a ligand-independent manner and positively regulated FLS2/BAK1 complex formation upon MAMP treatment. Finally, ios1 mutants were defective in BABA-induced resistance and priming. This work reveals IOS1 as a regulatory protein of FLS2- and EFR-mediated signaling that primes PTI activation upon bacterial elicitation.     

Blocking Single-Stranded Transferred DNA Conversion to Double-Stranded Intermediates by Overexpression of Yeast DNA REPLICATION FACTOR A

Agrobacterium tumefaciens delivers its single-stranded transferred DNA (T-strand) into the host cell nucleus, where it can be converted into double-stranded molecules. Various studies have revealed that double-stranded transfer DNA (T-DNA) intermediates can serve as substrates by as yet uncharacterized integration machinery. Nevertheless, the possibility that T-strands are themselves substrates for integration cannot be ruled out. We attempted to block the conversion of T-strands into double-stranded intermediates prior to integration in order to further investigate the route taken by T-DNA molecules on their way to integration. Transgenic tobacco (Nicotiana benthamiana) plants that overexpress three yeast (Saccharomyces cerevisiae) protein subunits of DNA REPLICATION FACTOR A (RFA) were produced. In yeast, these subunits (RFA1–RFA3) function as a complex that can bind single-stranded DNA molecules, promoting the repair of genomic double strand breaks. Overexpression of the RFA complex in tobacco resulted in decreased T-DNA expression, as determined by infection with A. tumefaciens cells carrying the β-glucuronidase intron reporter gene. Gene expression was not blocked when the reporter gene was delivered by microbombardment. Enhanced green fluorescent protein-assisted localization studies indicated that the three-protein complex was predominantly nuclear, thus indicating its function within the plant cell nucleus, possibly by binding naked T-strands and blocking their conversion into double-stranded intermediates. This notion was further supported by the inhibitory effect of RFA expression on the cell-to-cell movement of Bean dwarf mosaic virus, a single-stranded DNA virus. The observation that RFA complex plants dramatically inhibited the transient expression level of T-DNA and only reduced T-DNA integration by 50% suggests that double-stranded T-DNA intermediates, as well as single-stranded T-DNA, play significant roles in the integration process.Genetic transformation of plant cells by Agrobacterium tumefaciens represents a unique case of transkingdom DNA transfer (Stachel and Zambryski, 1989; Tzfira and Citovsky, 2002; Lacroix and Citovsky, 2013). This bacterium creates crown galls by transforming plant cells with a part of its Ti plasmid, the transfer DNA (T-DNA), at the infection site. The T-DNA, which integrates into the plant genome, contains genes encoding for enzymes involved in the production, modification, and alteration of plant growth regulators‎ and in the production of tumor-specific metabolites called opines. Expression of the integrated T-DNA, therefore, results in uncontrolled cell division and the formation of tumors (Gaudin et al., 1994; Das, 1998).The route that takes the T-DNA from the bacterium to the plant cell nucleus occurs in three major steps. It begins inside A. tumefaciens, where the virulence proteins VirD1 and VirD2 are responsible for processing the single-stranded T-DNA. The T-strand with one VirD2 molecule covalently attached to its 5′ end (Herrera-Estrella et al., 1988; Young and Nester, 1988) is then exported, together with several other virulence proteins, through the bacterial type IV secretion system, where it is most likely coated with many VirE2 molecules, becoming the transported form of the T-DNA, the transport complex (Dumas et al., 2001). VirE2 is probably translocated to the plant cell independently of the VirD2-conjugated T-strand along with other A. tumefaciens effector proteins (Otten et al., 1984; Sundberg et al., 1996). Moreover, VirE2 binds to the T-strand in the plant and thus provides protection from nuclease attack inside the plant cells (Yusibov et al., 1994). Abu-Arish et al. (2004) and Citovsky et al. (1997) used the bacteriophage M13 single-stranded DNA (ssDNA) mixed with purified VirE2 molecules to gain direct insight into the transport complex structure. Electron microscopy and single-particle image-processing methods yielded a better understanding of the transport complex structure. During the last step on the way to the nucleus, VirD2 and VirE2 are thought to assist the import of the transport complex into the host cell nucleus (Howard et al., 1992; Rossi et al., 1993; Citovsky, 1994; Ziemienowicz, 2001), whereas phosphorylated VirE2 INTERACTED PROTEIN1 (VIP1; Djamei et al., 2007; Dafny-Yelin et al., 2008) functions as a molecular linker between VirE2 and KARYOPHERIN-α (KAPα; Tzfira and Citovsky, 2002), allowing VirE2 to use the host cell nuclear import machinery (Tzfira et al., 2001; Citovsky et al., 2004; Anand et al., 2007).Once inside the nucleus, the transport complex is the substrate destined for integration. Two different models have been suggested for the T-DNA integration, double-stranded break (DSB) repair and single-stranded gap repair (SSGR; Gheysen et al., 1991; Mayerhofer et al., 1991). The DSB model predicts that unwound ends of a double-stranded T-DNA molecule anneal with single-stranded overhangs of DSBs in the plant DNA, the residual 5′ and 3′ overhangs are removed, and the inserted T-DNA is ligated. Mutations in the Arabidopsis (Arabidopsis thaliana) RADIATION-SENSITIVE52 (RAD52) gene that plays an essential role in homology-dependent DSB repair and recombination (Symington, 2002) decrease the levels of intrachromosomal recombination compared with wild-type plants (Samach et al., 2011). Recent studies further supported the notion that the T-strand molecule becomes double stranded prior to integration. For example, a direct indication of the involvement of double-stranded integration intermediates came from the detection of T-DNA inserts within the sites of DSB repair in the host DNA, which suggested ligation of double-stranded T-DNA molecules to both sides of the break made using a rear-cutting restriction enzyme (Salomon and Puchta, 1998; Chilton and Que, 2003; Tzfira et al., 2003). Recent evidence shows that T-DNA molecules can be converted into double-stranded T-DNA molecules using T-strand priming (Liang and Tzfira, 2013), and while double-stranded T-DNA molecules may serve as substrates for integration (Chilton and Que, 2003; Tzfira et al., 2003), a recent study showed that double-stranded T-DNA molecules can circularize and may end up as a dead ends for the integration process (Singer ‎et al., 2012). The SSGR model was established as the dominant model for T-DNA integration in plant cells based on two major observations. First, VirD2 is able not only to digest but also to rejoin single-stranded substrates in vitro (Pansegrau et al., 1993). This led to the suggestion that VirD2 may function as the T-DNA ligase in plant cells and, by implication, that T-DNAs integrate as single-stranded molecules. Second, specific mutations at the VirD2 putative integrase motif resulted in small deletions at the 5′ end of the T-DNA molecules (Tinland et al., 1995). Therefore, Tinland et al. (1995) revisited the SSGR integration model to the microhomology-dependent integration model, suggesting that only short sequences of the T-DNA molecule actually anneal to preintegration genomic sites (Tzfira et al., 2004a; Windels et al., 2008; Ziemienowicz et al., 2008).The DSB model suggests that the transport complex is first stripped of its attached protein in the nucleus and then arrives at the integration site as double-stranded DNA (dsDNA). However, in the SSGR model, the transport complex itself reaches the site of integration and then probably degrades during the integration process. Evidence for a physical connection between the transport complex and the chromatin was presented by Loyter et al. (2005), who found that VIP1 acts as a molecular linker between the transport complex and the histone constituents of the host chromatin. When the transport complex reaches the chromatin, VIP1 becomes polyubiquitinated by VirF or Skp1/Cullin/F-box protein VIP1-binding F-box [SCF(VBF); Zaltsman et al., 2010, 2013] containing a proteolysis complex, and after the protein complex is degraded, the single-stranded T-DNA remains naked, with only VirD2 attached to its right border (Magori and Citovsky, 2011).We overexpressed the ssDNA-binding protein REPLICATION FACTOR A (RFA) from yeast (Saccharomyces cerevisiae) in order to further characterize the route that takes the transport complex to the integration site through double- or single-stranded forms. Previous work shows that overexpression of an ssDNA-binding protein from Escherichia coli (i.e. the recombination protein A) can function in plant cells and can interact with or supplement the endogenous plant recombination machinery (Reiss et al., 1996).RFA from yeast is a tightly associated complex composed of three subunits of 69, 36, and 13 kD, termed RFA1, RFA2, and RFA3, respectively (Longhese et al., 1994). Hays et al. (1998) suggested a role for RFA in recruiting DNA polymerase to the site of a DSB via simultaneous interactions with RAD52 and a repair polymerase, in order to protect the exposed single-stranded ends from cellular nucleases (Smith and Rothstein, 1995; Park et al., 1996; Hays et al., 1998). RFA heterologous proteins have been found in plants, but their function in T-DNA integration and their involvement in the DNA-repair mechanism are still unknown. In this study, we investigated the effect of the RFA complex from yeast on the T-DNA integration mechanism in the plant cell nucleus and report that overexpression of the RFA complex (Rex) in tobacco (Nicotiana benthamiana) plants almost completely blocks the T-DNA’s transient and reduced stable transformation, probably by binding to single-stranded T-DNA, and prevents its expression and integration through the DSB pathway. Moreover, we show that the movement of Bean dwarf mosaic virus (BDMV; Begomovirus: Geminiviridae), a single-stranded virus, is inhibited in the Rex-transformed plant.     

Mycorrhizal networks: common goods of plants shared under unequal terms of trade

Plants commonly live in a symbiotic association with arbuscular mycorrhizal fungi (AMF). They invest photosynthetic products to feed their fungal partners, which, in return, provide mineral nutrients foraged in the soil by their intricate hyphal networks. Intriguingly, AMF can link neighboring plants, forming common mycorrhizal networks (CMNs). What are the terms of trade in such CMNs between plants and their shared fungal partners? To address this question, we set up microcosms containing a pair of test plants, interlinked by a CMN of Glomus intraradices or Glomus mosseae. The plants were flax (Linum usitatissimum; a C₃ plant) and sorghum (Sorghum bicolor; a C₄ plant), which display distinctly different ¹³C/¹²C isotope compositions. This allowed us to differentially assess the carbon investment of the two plants into the CMN through stable isotope tracing. In parallel, we determined the plants’ “return of investment” (i.e. the acquisition of nutrients via CMN) using ¹⁵N and ³³P as tracers. Depending on the AMF species, we found a strong asymmetry in the terms of trade: flax invested little carbon but gained up to 94% of the nitrogen and phosphorus provided by the CMN, which highly facilitated growth, whereas the neighboring sorghum invested massive amounts of carbon with little return but was barely affected in growth. Overall biomass production in the mixed culture surpassed the mean of the two monocultures. Thus, CMNs may contribute to interplant facilitation and the productivity boosts often found with intercropping compared with conventional monocropping.Arbuscular mycorrhizal fungi (AMF) inhabit the soils of virtually all terrestrial ecosystems, forming symbiotic associations with most plants (Parniske, 2008; Smith and Read, 2008). The host plants incur substantial carbon costs to sustain this symbiosis (Jakobsen and Rosendahl, 1990), but in return, they obtain multiple benefits from the fungal partners, above all, the provision of mineral nutrients. AMF may supply up to 90% of the host plant’s nitrogen and phosphorus requirements (Smith and Read, 2008). Moreover, AMF are important determinants of plant community structure and ecosystem productivity (Grime et al., 1987; van der Heijden et al., 1998), and they represent a crucial asset for sustainable agriculture (Rooney et al., 2009). Typically, AMF exhibit little host specificity; a single individual may form a common mycorrhizal network (CMN) between several coexisting plant individuals, even from different species (Whitfield, 2007; Smith and Read, 2008; Bever et al., 2010). Such CMNs may be enlarged through hyphal fusion of conspecific AMF (Giovannetti et al., 2004). The functionality of CMNs formed by the fusion of two individual fungal networks by hyphal anastomoses has been demonstrated by tracing nutrient allocation between individual host plants upon the fusion of their associated CMNs (Mikkelsen et al., 2008).The potential role and importance of CMNs is most apparent in the case of mycoheterotrophic plants. These plants connect themselves to an existing CMN to receive both carbon and mineral nutrients (Bidartondo et al., 2002; Courty et al., 2011). There is an ongoing debate over whether carbon transfer through CMNs may also occur among autotrophic plants (Bever et al., 2010; Hodge et al., 2010). This is of a certain academic interest, but it may obscure a more general and obvious question arising from recent literature (Hodge et al., 2010; Hammer et al., 2011; Kiers et al., 2011; Smith and Smith, 2011; Fellbaum et al., 2012): What are the terms of trade between plants and their shared fungal partners? Put another way, what is the “investment” of a given plant into a CMN (in the currency of assimilated carbon), and what is the “return of investment” in terms of mineral nutrients provided by the CMN? Indeed, different cocultivated plants benefit differently from their CMN, depending on the AMF species involved, and these differences significantly affect plant coexistence (Zabinski et al., 2002; van der Heijden et al., 2003; Wagg et al., 2011). However, until now, the relationship between the carbon investment and the nutritional benefit of different plants engaged in a CMN has never been assessed.To address the terms of trade in a CMN experimentally, we established a model system consisting of two plant individuals growing side by side in compartmented microcosms (Fig. 1). The roots of the plants were confined to their respective “root hyphal compartments” (RHCs). In the treatments with AMF inoculation, however, the plants were able to connect through CMN in the “hyphal compartment” (HC) or in the “label-hyphal compartment” (LHC). We assessed the carbon investments of the single plants into the CMN through stable isotope tracing. To this end, we chose the C₃ plant flax (Linum usitatissimum) and the C₄ plant sorghum (Sorghum bicolor) for our experiments. Due to the different isotope fractionation during C₃ versus C₄ carbon fixation, these two species display distinctly different carbon isotope ratios (δ ¹³C approximately 33‰ for flax and approximately 14‰ for sorghum). This difference in the ¹³C signature of C₃ and C₄ plants has been widely used to track carbon flows in mycorrhizal symbioses (Allen and Allen, 1990; Fitter et al., 1998). The plants were grown either in “monocultures,” as a pair of identical plant species, or in a “mixed culture,” as a pair of different plant species. We used two different AMF species in the experiments for inoculation, Glomus intraradices and Glomus mosseae (recently renamed Glomus irregulare [Rhizophagus irregularis] and Funelliformis mosseae, respectively [Schüssler and Walker, 2010]). The chosen experimental setup allowed us to harvest the bulk of the CMN in the HC (Fig. 1) and to estimate the respective carbon investment of the two plants into the CMN through the analysis of the δ ¹³C of isolated AMF hyphae or, with higher precision, of the AMF-specific fatty acid C16:1ω5 (Olsson and Johnson, 2005). We estimated the return of investment with respect to nitrogen and phosphorus for each of the two plants using ¹⁵N and ³³P as tracers added to the LHC (Fig. 1). As a control, we also grew two monocultures and a mixed culture without any AMF inoculation.Open in a separate windowFigure 1.Compartmented microcosms to study the role of CMNs in monocultures and mixed culture. Microcosms, consisting of two plant individuals, were set up in compartmented containers subdivided by nylon mesh screens (25 and 65 μm, respectively, as indicated). Both types of screens are pervious for fungal hyphae but not for roots and allow the separation into two RHCs, a HC, and a LHC for supplying ¹⁵N and ³³P labels. The plants used were flax (F) and sorghum (S) either as a pair of conspecific plants (F:F, S:S) as a model of monoculture or in combination (F:S) as a model of a mixed culture.     

Lack of Phosphatidylglycerol Inhibits Chlorophyll Biosynthesis at Multiple Sites and Limits Chlorophyllide Reutilization in Synechocystis sp. Strain PCC 6803

The negatively charged lipid phosphatidylglycerol (PG) constitutes up to 10% of total lipids in photosynthetic membranes, and its deprivation in cyanobacteria is accompanied by chlorophyll (Chl) depletion. Indeed, radioactive labeling of the PG-depleted ΔpgsA mutant of Synechocystis sp. strain PCC 6803, which is not able to synthesize PG, proved the inhibition of Chl biosynthesis caused by restriction on the formation of 5-aminolevulinic acid and protochlorophyllide. Although the mutant accumulated chlorophyllide, the last Chl precursor, we showed that it originated from dephytylation of existing Chl and not from the block in the Chl biosynthesis. The lack of de novo-produced Chl under PG depletion was accompanied by a significantly weakened biosynthesis of both monomeric and trimeric photosystem I (PSI) complexes, although the decrease in cellular content was manifested only for the trimeric form. However, our analysis of ΔpgsA mutant, which lacked trimeric PSI because of the absence of the PsaL subunit, suggested that the virtual stability of monomeric PSI is a result of disintegration of PSI trimers. Interestingly, the loss of trimeric PSI was accompanied by accumulation of monomeric PSI associated with the newly synthesized CP43 subunit of photosystem II. We conclude that the absence of PG results in the inhibition of Chl biosynthetic pathway, which impairs synthesis of PSI, despite the accumulation of chlorophyllide released from the degraded Chl proteins. Based on the knowledge about the role of PG in prokaryotes, we hypothesize that the synthesis of Chl and PSI complexes are colocated in a membrane microdomain requiring PG for integrity.Photosynthetic membrane of oxygenic phototrophs has a unique lipid composition that has been conserved during billions of years of evolution from cyanobacteria and algae to modern higher plants. With no known exception, this membrane system always contains the uncharged glycolipids monogalactosyldiacylglycerol and digalactosyldiacylglycerol (DGDG) as well as the negatively charged lipids sulfoquinovosyldiacylglycerol (SQDG) and phosphatidylglycerol (PG; Murata and Siegenthaler, 1998). Interestingly, it seems that PG is the only lipid completely essential for the oxygenic photosynthesis. The loss of DGDG has only a mild impact on the cyanobacterial cell (Awai et al., 2007), and as shown recently in the cyanobacterium Synechocystis sp. strain PCC 6803, both galactolipids can be in fact replaced by glucolipids (Awai et al., 2014). SQDG and PG are only minor lipid components, each accounting for 5% to 12% of total lipids (Murata and Siegenthaler, 1998). SQDG is dispensable, although its lack results in various defects (Yu et al., 2002; Aoki et al., 2004), but PG plays an essential role in both cyanobacterial cells and plant chloroplasts (Hagio et al., 2000; Babiychuk et al., 2003).The critical role of PG has been mostly connected to the function of PSII. In both cyanobacteria and plants, lack of PG impairs the stability of PSII complexes and the electron transport between primary and secondary quinone acceptors inside the PSII reaction center. As shown in Synechocystis sp., PG molecules stabilize PSII dimers and facilitate the binding of inner antenna protein CP43 within the PSII core (Laczkó-Dobos et al., 2008). Indeed, according to the PSII crystal structure, two PG molecules are located at the interface between CP43 and the D1-D2 heterodimer (Guskov et al., 2009). As a consequence, the PG depletion inhibits and destabilizes PSII complexes and also, impairs assembly of new PSII complexes, although all PSII subunits are still synthesized in the cell (Laczkó-Dobos et al., 2008).Despite the fact that the vital link between PG and PSII is now well established, the phenotypic traits of PG-depleted cells signal that there are other sites in the photosynthetic membrane requiring strictly PG molecules. In Synechocystis sp., lack of PG triggers rapid loss of trimeric PSI complexes (Domonkos et al., 2004; Sato et al., 2004), and because PSI complexes bind more than 80% of chlorophyll (Chl) in the Synechocystis sp. cell, the PG depletion is accompanied by a characteristic Chl bleaching (Domonkos et al., 2004). However, the reasons for this symptom are still unclear. Chl metabolism is tightly coordinated with synthesis, assembly, and degradation of photosystem complexes (for review, see Komenda et al., 2012b; Sobotka, 2014), and we have shown recently that the PSI complexes are the main sink for de novo Chl produced in cyanobacteria (Kopečná et al., 2012). Given the drastic decrease in PSI content in the PG-depleted cells, Chl biosynthesis must be directly or indirectly affected after the PG concentration in membranes drops below a critical value. Although it was recently suggested that galactolipid and Chl biosyntheses are coregulated during chloroplast biogenesis (Kobayashi et al., 2014), a response of the Chl biosynthetic pathway to the altered lipid content has not been examined.To investigate Chl metabolism during PG starvation, we used the Synechocystis sp. ΔpgsA mutant, which is unable to synthesize PG (Hagio et al., 2000). The advantage of using the ΔpgsA strain is in its ability to utilize exogenous PG from growth medium, which allows monitoring of phenotypic changes from a wild type-like situation to completely PG-depleted cells. Chl biosynthesis shares the same metabolic pathway with heme and other tetrapyrroles. At the beginning of tetrapyrrole biosynthesis, the initial precursor, 5-aminolevulinic acid (ALA), is made from Glu through glutamyl-tRNA and subsequently converted in several steps to protoporphyrin IX. The pathway branches at the point where protoporphyrin IX is chelated by magnesium to produce Mg-protoporphyrin IX, the first intermediate on the Chl branch. This step is catalyzed by Mg-chelatase, a multisubunit enzyme that associates relatively weakly with the membrane; however, all following enzymes downward in the pathway are almost exclusively bound to membranes (Masuda and Fujita, 2008; Kopečná et al., 2012). The last enzyme of the Chl pathway, Chl synthase, is an integral membrane protein that attaches a phytyl chain to the last intermediate chlorophyllide (Chlide) to finalize Chl formation (Oster et al., 1997; Addlesee et al., 2000). According to current views, Chl synthase should also be involved in reutilization of Chl molecules from degraded Chl-binding proteins, which includes dephytylation and phytylation of Chl molecules with Chlide as an intermediate (Vavilin and Vermaas, 2007).In this study, we show a complex impact of PG deficiency on Chl metabolism. The lack of PG inhibited Chl biosynthesis at the two different steps: first, it drastically reduced formation of the initial precursor ALA, and second, it impaired the Mg-protoporphyrin methyl ester IX (MgPME) cyclase enzyme catalyzing synthesis of protochlorophyllide (Pchlide). The diminished rate of Chl formation was accompanied by impaired synthesis of both trimeric and monomeric PSI complexes and accumulation of a PSI monomer associated with the CP43 subunit of PSII. We also showed that the PG-depleted cells accumulated Chlide, originating from dephytylation of existing Chl, which suggests an inability to reutilize Chl for the PSI synthesis. We discuss a scenario that the Chl biosynthesis and synthesis of core PSI subunits are colocated in PG-enriched membrane microdomains.     

PsbN Is Required for Assembly of the Photosystem II Reaction Center in Nicotiana tabacum

The chloroplast-encoded low molecular weight protein PsbN is annotated as a photosystem II (PSII) subunit. To elucidate the localization and function of PsbN, encoded on the opposite strand to the psbB gene cluster, we raised antibodies and inserted a resistance cassette into PsbN in both directions. Both homoplastomic tobacco (Nicotiana tabacum) mutants ∆psbN-F and ∆psbN-R show essentially the same PSII deficiencies. The mutants are extremely light sensitive and failed to recover from photoinhibition. Although synthesis of PSII proteins was not altered significantly, both mutants accumulated only ∼25% of PSII proteins compared with the wild type. Assembly of PSII precomplexes occurred at normal rates, but heterodimeric PSII reaction centers (RCs) and higher order PSII assemblies were not formed efficiently in the mutants. The ∆psbN-R mutant was complemented by allotopic expression of the PsbN gene fused to the sequence of a chloroplast transit peptide in the nuclear genome. PsbN represents a bitopic trans-membrane peptide localized in stroma lamellae with its highly conserved C terminus exposed to the stroma. Significant amounts of PsbN were already present in dark-grown seedling. Our data prove that PsbN is not a constituent subunit of PSII but is required for repair from photoinhibition and efficient assembly of the PSII RC.     

One Divinyl Reductase Reduces the 8-Vinyl Groups in Various Intermediates of Chlorophyll Biosynthesis in a Given Higher Plant Species,But the Isozyme Differs between Species

Divinyl reductase (DVR) converts 8-vinyl groups on various chlorophyll intermediates to ethyl groups, which is indispensable for chlorophyll biosynthesis. To date, five DVR activities have been detected, but adequate evidence of enzymatic assays using purified or recombinant DVR proteins has not been demonstrated, and it is unclear whether one or multiple enzymes catalyze these activities. In this study, we systematically carried out enzymatic assays using four recombinant DVR proteins and five divinyl substrates and then investigated the in vivo accumulation of various chlorophyll intermediates in rice (Oryza sativa), maize (Zea mays), and cucumber (Cucumis sativus). The results demonstrated that both rice and maize DVR proteins can convert all of the five divinyl substrates to corresponding monovinyl compounds, while both cucumber and Arabidopsis (Arabidopsis thaliana) DVR proteins can convert three of them. Meanwhile, the OsDVR (Os03g22780)-inactivated 824ys mutant of rice exclusively accumulated divinyl chlorophylls in its various organs during different developmental stages. Collectively, we conclude that a single DVR with broad substrate specificity is responsible for reducing the 8-vinyl groups of various chlorophyll intermediates in higher plants, but DVR proteins from different species have diverse and differing substrate preferences, although they are homologous.Chlorophyll (Chl) molecules universally exist in photosynthetic organisms. As the main component of the photosynthetic pigments, Chl molecules perform essential processes of absorbing light and transferring the light energy in the reaction center of the photosystems (Fromme et al., 2003). Based on the number of vinyl side chains, Chls are classified into two groups, 3,8-divinyl (DV)-Chl and 3-monovinyl (MV)-Chl. The DV-Chl molecule contains two vinyl groups at positions 3 and 8 of the tetrapyrrole macrocycle, whereas the MV-Chl molecule contains a vinyl group at position 3 and an ethyl group at position 8 of the macrocycle. Almost all of the oxygenic photosynthetic organisms contain MV-Chls, with the exceptions of some marine picophytoplankton species that contain only DV-Chls as their primary photosynthetic pigments (Chisholm et al., 1992; Goericke and Repeta, 1992; Porra, 1997).The classical single-branched Chl biosynthetic pathway proposed by Granick (1950) and modified by Jones (1963) assumed the rapid reduction of the 8-vinyl group of DV-protochlorophyllide (Pchlide) catalyzed by a putative 8-vinyl reductase. Ellsworth and Aronoff (1969) found evidence for both MV and DV forms of several Chl biosynthetic intermediates between magnesium-protoporphyrin IX monomethyl ester (MPE) and Pchlide in Chlorella spp. mutants. Belanger and Rebeiz (1979, 1980) reported that the Pchlide pool of etiolated higher plants contains both MV- and DV-Pchlide. Afterward, following the further detection of MV- and DV-tetrapyrrole intermediates and their biosynthetic interconversion in tissues and extracts of different plants (Belanger and Rebeiz, 1982; Duggan and Rebeiz, 1982; Tripathy and Rebeiz, 1986, 1988; Parham and Rebeiz, 1992, 1995; Kim and Rebeiz, 1996), a multibranched Chl biosynthetic heterogeneity was proposed (Rebeiz et al., 1983, 1986, 1999; Whyte and Griffiths, 1993; Kolossov and Rebeiz, 2010).Biosynthetic heterogeneity refers to the biosynthesis of a particular metabolite by an organelle, tissue, or organism via multiple biosynthetic routes. Varieties of reports lead to the assumption that Chl biosynthetic heterogeneity originates mainly in parallel DV- and MV-Chl biosynthetic routes. These routes are interconnected by 8-vinyl reductases that convert DV-tetrapyrroles to MV-tetrapyrroles by conversion of the vinyl group at position 8 of ring B to the ethyl group (Parham and Rebeiz, 1995; Rebeiz et al., 2003). DV-MPE could be converted to MV-MPE in crude homogenates from etiolated wheat (Triticum aestivum) seedlings (Ellsworth and Hsing, 1974). Exogenous DV-Pchlide could be partially converted to MV-Pchlide in barley (Hordeum vulgare) plastids (Tripathy and Rebeiz, 1988). 8-Vinyl chlorophyllide (Chlide) a reductases in etioplast membranes isolated from etiolated cucumber (Cucumis sativus) cotyledons and barley and maize (Zea mays) leaves were found to be very active in the conversion of exogenous DV-Chlide a to MV-Chlide a (Parham and Rebeiz, 1992, 1995). Kim and Rebeiz (1996) suggested that Chl biosynthetic heterogeneity in higher plants may originate at the level of DV magnesium-protoporphyrin IX (Mg-Proto) and would be mediated by the activity of a putative 8-vinyl Mg-Proto reductase in barley etiochloroplasts and plastid membranes. However, since these reports did not use purified or recombinant enzyme, it is not clear whether the reductions of the 8-vinyl groups of various Chl intermediates are catalyzed by one enzyme of broad specificity or by multiple enzymes of narrow specificity, which actually has become one of the focus issues in Chl biosynthesis.Nagata et al. (2005) and Nakanishi et al. (2005) independently identified the AT5G18660 gene of Arabidopsis (Arabidopsis thaliana) as an 8-vinyl reductase, namely, divinyl reductase (DVR). Chew and Bryant (2007) identified the DVR BciA (CT1063) gene of the green sulfur bacterium Chlorobium tepidum, which is homologous to AT5G18660. An enzymatic assay using a recombinant Arabidopsis DVR (AtDVR) on five DV substrates revealed that the major substrate of AtDVR is DV-Chlide a, while the other four DV substrates could not be converted to corresponding MV compounds (Nagata et al., 2007). Nevertheless, a recombinant BciA is able to reduce the 8-vinyl group of DV-Pchlide to generate MV-Pchlide (Chew and Bryant, 2007). Recently, we identified the rice (Oryza sativa) DVR encoded by Os03g22780 that has sequence similarity with the Arabidopsis DVR gene AT5G18660. We also confirmed that the recombinant rice DVR (OsDVR) is able to not only convert DV-Chlide a to MV-Chlide a but also to convert DV-Chl a to MV-Chl a (Wang et al., 2010). Thus, it is possible that the reductions of the 8-vinyl groups of various Chl biosynthetic intermediates are catalyzed by one enzyme of broad specificity.In this report, we extended our studies to four DVR proteins and five DV substrates. First, ZmDVR and CsDVR genes were isolated from maize and cucumber genomes, respectively, using a homology-based cloning approach. Second, enzymatic assays were systematically carried out using recombinant OsDVR, ZmDVR, CsDVR, and AtDVR as representative DVR proteins and using DV-Chl a, DV-Chlide a, DV-Pchlide a, DV-MPE, and DV-Mg-Proto as DV substrates. Third, we examined the in vivo accumulations of various Chl intermediates in rice, maize, and cucumber. Finally, we systematically investigated the in vivo accumulations of Chl and its various intermediates in the OsDVR (Os03g22780)-inactivated 824ys mutant of rice (Wang et al., 2010). The results strongly suggested that a single DVR protein with broad substrate specificity is responsible for reducing the 8-vinyl groups of various intermediate molecules of Chl biosynthesis in higher plants, but DVR proteins from different species could have diverse and differing substrate preferences even though they are homologous.     

Phylobiochemical Characterization of Class-Ib Aspartate/Prephenate Aminotransferases Reveals Evolution of the Plant Arogenate Phenylalanine Pathway

The aromatic amino acid Phe is required for protein synthesis and serves as the precursor of abundant phenylpropanoid plant natural products. While Phe is synthesized from prephenate exclusively via a phenylpyruvate intermediate in model microbes, the alternative pathway via arogenate is predominant in plant Phe biosynthesis. However, the molecular and biochemical evolution of the plant arogenate pathway is currently unknown. Here, we conducted phylogenetically informed biochemical characterization of prephenate aminotransferases (PPA-ATs) that belong to class-Ib aspartate aminotransferases (AspAT Ibs) and catalyze the first committed step of the arogenate pathway in plants. Plant PPA-ATs and succeeding arogenate dehydratases (ADTs) were found to be most closely related to homologs from Chlorobi/Bacteroidetes bacteria. The Chlorobium tepidum PPA-AT and ADT homologs indeed efficiently converted prephenate and arogenate into arogenate and Phe, respectively. A subset of AspAT Ib enzymes exhibiting PPA-AT activity was further identified from both Plantae and prokaryotes and, together with site-directed mutagenesis, showed that Thr-84 and Lys-169 play key roles in specific recognition of dicarboxylic keto (prephenate) and amino (aspartate) acid substrates. The results suggest that, along with ADT, a gene encoding prephenate-specific PPA-AT was transferred from a Chlorobi/Bacteroidetes ancestor to a eukaryotic ancestor of Plantae, allowing efficient Phe and phenylpropanoid production via arogenate in plants today.     

HYPERSENSITIVE TO HIGH LIGHT1 Interacts with LOW QUANTUM YIELD OF PHOTOSYSTEM II1 and Functions in Protection of Photosystem II from Photodamage in Arabidopsis

Under high-irradiance conditions, plants must efficiently protect photosystem II (PSII) from damage. In this study, we demonstrate that the chloroplast protein HYPERSENSITIVE TO HIGH LIGHT1 (HHL1) is expressed in response to high light and functions in protecting PSII against photodamage. Arabidopsis thaliana hhl1 mutants show hypersensitivity to high light, drastically decreased PSII photosynthetic activity, higher nonphotochemical quenching activity, a faster xanthophyll cycle, and increased accumulation of reactive oxygen species following high-light exposure. Moreover, HHL1 deficiency accelerated the degradation of PSII core subunits under high light, decreasing the accumulation of PSII core subunits and PSII–light-harvesting complex II supercomplex. HHL1 primarily localizes in the stroma-exposed thylakoid membranes and associates with the PSII core monomer complex through direct interaction with PSII core proteins CP43 and CP47. Interestingly, HHL1 also directly interacts, in vivo and in vitro, with LOW QUANTUM YIELD OF PHOTOSYSTEM II1 (LQY1), which functions in the repair and reassembly of PSII. Furthermore, the hhl1 lqy1 double mutants show increased photosensitivity compared with single mutants. Taken together, these results suggest that HHL1 forms a complex with LQY1 and participates in photodamage repair of PSII under high light.     

Stable Carbon Isotope Discrimination Is under Genetic Control in the C4 Species Maize with Several Genomic Regions Influencing Trait Expression

In plants with C₄ photosynthesis, physiological mechanisms underlying variation in stable carbon isotope discrimination (Δ13C) are largely unknown, and genetic components influencing Δ13C have not been described. We analyzed a maize (Zea mays) introgression library derived from two elite parents to investigate whether Δ13C is under genetic control in this C₄ species. High-density genotyping with the Illumina MaizeSNP50 Bead Chip was used for a detailed structural characterization of 89 introgression lines. Phenotypic analyses were conducted in the field and in the greenhouse for kernel Δ13C as well as plant developmental and photosynthesis-related traits. Highly heritable significant genetic variation for Δ13C was detected under field and greenhouse conditions. For several introgression library lines, Δ13C values consistently differed from the recurrent parent within and across the two phenotyping platforms. Δ13C was significantly associated with 22 out of 164 analyzed genomic regions, indicating a complex genetic architecture of Δ13C. The five genomic regions with the largest effects were located on chromosomes 1, 2, 6, 7, and 9 and explained 55% of the phenotypic variation for Δ13C. Plant development stage had no effect on Δ13C expression, as phenotypic as well as genotypic correlations between Δ13C, flowering time, and plant height were not significant. To our knowledge, this is the first study demonstrating Δ13C to be under polygenic control in the C₄ species maize.During photosynthesis, plants use light energy to convert atmospheric CO₂ and water into carbohydrates. For the element carbon, there are two stable isotopes, ¹²C and ¹³C. Due to the physical and chemical properties of photosynthetic CO₂ fixation, plants are depleted in ¹³C compared with atmospheric CO₂. In C₃ plants, this discrimination of stable carbon isotopes (Δ13C) has long been used to detect genetic differences of water use efficiency and has been shown to be an accurate predictor for yield under drought (Rebetzke et al., 2002). As Δ13C is linearly related to the ratio of intercellular to atmospheric CO₂ partial pressure (Farquhar et al., 1982), stomatal closure under drought stress is associated with reduced Δ13C. For C₄ plants, our knowledge about the mechanisms underlying Δ13C and about its association with water use efficiency is much more limited. Differences in Δ13C between genotypes of C₄ species have been reported, among others, for sorghum (Sorghum bicolor; Hubick et al., 1990) and maize (Zea mays; Monneveux et al., 2007). However, comprehensive studies analyzing the inheritance of Δ13C have not been performed to date.In C₃ plants, the important steps of CO₂ uptake include the diffusion of atmospheric CO₂ through the boundary layer and the stomata. Subsequently, CO₂ is taken up by the cell and enters the chloroplast, where carboxylation by Rubisco takes place. During photosynthetic carbon fixation, the strongest fractionation of carbon isotopes occurs during the carboxylation reaction of Rubisco (Roeske and O’Leary, 1984). A theoretical model of Δ13C in C₃ photosynthesis has been described by Farquhar et al. (1982), in which Δ13C depends linearly on the ratio of intercellular to ambient partial pressure of CO₂ (p_i p_a−1), and thus provides an indication of stomatal conductance and photosynthetic capacity. Additionally, the model includes the dependency of Δ13C on the fractionation of carbon isotopes during CO₂ diffusion in the air and on the enzymatic properties of the Rubisco enzyme.For rice (Oryza sativa), tomato (Solanum lycopersicum), and wheat (Triticum aestivum), it has been shown that genetic variation for Δ13C is quantitative, genotype-by-environment interaction is small, and the trait heritability is high (Condon and Richards, 1992; Rebetzke et al., 2002; Comstock et al., 2005; Impa et al., 2005). Quantitative trait loci (QTL) for Δ13C have been mapped (Handley et al., 1994; Price et al., 2002; Rebetzke et al., 2008), and in the model plant Arabidopsis (Arabidopsis thaliana), four genes have been identified that are associated with Δ13C. Two are involved in stomatal patterning and thus influence stomatal conductance (Masle et al., 2005; Nilson and Assmann, 2010), and one of them influences photosynthetic capacity as well (Masle et al., 2005). One gene plays a role in cuticular wax composition and is also associated with stomatal conductance (Lü et al., 2012), whereas the fourth gene encodes a cellulose synthase subunit, and mutations in this gene lead to decreased Δ13C. Presumably, this is the result of a decreased cell turgor due to a decreased water transport capacity of the xylem (Liang et al., 2010).For C₄ plants, our knowledge about the genetic mechanisms and physiological processes underlying Δ13C is much more limited, due to the more complex mechanism of CO₂ fixation. The first carboxylation step in C₄ plants takes place in mesophyll cells, in which CO₂ is fixed by phosphoenolpyruvate carboxylase (PEPC). During this reaction, combined with the fractionation of carbon isotopes during HCO₃⁻ formation, carbon is actually enriched in ¹³C (Farquhar, 1983). The C₄ organic acid formed by PEPC is transported to the bundle sheath cells, where CO₂ is released to be fixed by Rubisco in the second step. However, a fraction of CO₂ released in the bundle sheath can diffuse back to the mesophyll cells. The proportion of carbon fixed by PEPC that subsequently leaks out of the bundle sheath cells is termed leakiness (ϕ) and reduces the opportunity of Rubisco to discriminate against ¹³C in C₄ plants. According to the theoretical model by Farquhar (1983), Δ13C and p_i p_a−1 are also linearly related in C₄ plants, but the regression slope is determined by ϕ. Consequently, there can be a positive or a negative correlation of Δ13C and p_i p_a−1 depending on ϕ (Hubick et al., 1990). Regarding the entire fixation process, discrimination against ¹³C in C₄ plants is not as strong as in C₃ plants, and so far there have been few studies reporting a genetic variation of Δ13C in C₄ plants. In sorghum, small but significant differences in Δ13C have been observed among 12 cultivars (Hubick et al., 1990), and similar to C₃ plants, Δ13C has been shown to be correlated with transpiration efficiency (Henderson et al., 1998). Additionally, it has been shown for maize and sugarcane (Saccharum officinarum) that stress conditions lead to an increase in Δ13C (Bowman et al., 1989; Meinzer et al., 1994; Ranjith et al., 1995; Buchmann et al., 1996). Experiments under drought and under well-watered conditions showed higher values for Δ13C in drought-tolerant maize hybrids than in susceptible checks (Monneveux et al., 2007).The use of Δ13C as an indirect trait in breeding for drought tolerance in C₄ species would be highly beneficial, given a stable trait expression and high heritability similar to that in C₃ plants. To assess whether Δ13C can also be used in C₄ plants as an indirect selection trait for drought-tolerant lines, it needs to be shown that Δ13C is under genetic control, although the physiology and molecular mechanisms of Δ13C are not yet fully understood. In this study, we used an introgression library (IL; Eshed and Zamir, 1994) derived from two elite parents to analyze the genetic variation in Δ13C under well-watered conditions. ILs have been successfully used in genetics to identify QTL for various qualitatively and quantitatively inherited traits. An IL is a defined set of nearly isogenic inbred lines derived from repeated backcrosses with one of the parents (recurrent parent [RP]) and marker-assisted selection for single fragments (Supplemental Fig. S1). Ideally, each IL line carries a single chromosome fragment of a donor parent (DP) in the genetic background of an RP. Taken together, the different segments cover the whole donor genome, allowing estimation of the effects of single donor fragments in an otherwise identical genetic background (Eshed and Zamir, 1994). The RP of the IL under investigation originates from southeastern Europe and is an elite inbred line of the maize dent pool. As DP, we chose an unrelated maize line representative of the European flint pool. The IL (IL_01–IL_89) was genotyped using the Illumina MaizeSNP50 Bead Chip (Ganal et al., 2011) carrying 56,110 single-nucleotide polymorphism (SNP) markers.Kernel Δ13C of 77 IL lines was measured in the field and in the greenhouse (Δ13C is genetically controlled in the C₄ species maize. Our specific goals were (1) to characterize the genetic architecture of Δ13C (i.e. to determine the number of genomic regions associated with Δ13C), (2) to localize genomic regions influencing Δ13C, and (3) to assess the extent to which genotypic variation in Δ13C might be the result of differences in plant development.

Table I.

Overview of the experiments and experimental designs