Identification of a type I Ca2+/Mg2+-dependent endonuclease induced in maize cells exposed to camptothecin
© Sánchez-Pons and Vicient; licensee BioMed Central Ltd. 2013
Received: 19 July 2013
Accepted: 16 November 2013
Published: 20 November 2013
Camptothecin is a plant alkaloid that specifically binds topoisomerase I, inhibiting its activity and inducing double stranded breaks in DNA and activating the cell responses to DNA damage.
Maize cultured cells were incubated in the presence of different concentrations of camptothecin. Camptothecin inhibits cultured cell growth, induces genomic DNA degradation, and induces a 32 kDa Ca2+/Mg2+-dependent nuclease activity. This nuclease, we called CaMNUC32, is inhibited by Zn2+ and by acid pH, it is mainly localized in the nucleus and it cleaves single- and double-stranded DNA, with a higher activity against single-stranded DNA. Two-dimensional electrophoresis combined with mass spectrometry suggests that CaMNUC32 is a member of the type I S1/P1 nuclease family. This type of nucleases are usually Zn2+-dependent but our results support previous indications that S1-type nucleases have a wide variety of enzyme activities, including Ca2+/Mg2+-dependent.
We have identified and characterized CaMNUC32, a 32 kDa Ca2+/Mg2+-dependent nuclease of the S1/P1 family induced by the topoisomerase I inhibitor camptothecin in maize cultured cells.
KeywordsCamptothecin DNA degradation Maize Nuclease
Topoisomerase I (TOPI) is an enzyme which catalyses the relaxation of super coiled DNA by cleaving and re-joining one DNA strand . TOPI activity is essential in dividing cells to release the torsion created by the progression of DNA replication forks. Camptothecin (CPT) is a plant alkaloid that specifically binds to TOPI, stabilizing the complexes formed between DNA and TOPI . The collisions between the trapped TOPI-CPT complexes and the replication fork during DNA replication produce DNA breaks, which induce DNA damage responses and, depending on the dose, cell death . CPT-induced DNA damage responses have also been observed in plants . For example, CPT induces DNA damage in maize immature embryos and induces the transcription of genes involved in DNA repair, the repression of genes involved in cell division, the accumulation of several proteins involved in stress responses and the induction of the activity of some nucleases . Nuclease activation in response to DNA damaging agents has been previously observed [6–8].
Eukaryotic nucleases are involved in several processes like DNA restriction, repair, recombination, transposition and programmed cell death (PCD) [9–11]. Plant nucleases can be classified into groups depending on their catalytic properties, mainly their divalent metal ion requirements. Plants have two major classes of endonucleases, Zn2+-dependent and Ca2+-dependent endonucleases [9, 12] and refereed articles. Some other subgroups have been identified whose nucleolytic activities are stimulated by other ions such as Mg2+, Mn2+ or Co2+.
Zn2+-dependent nucleases (also termed Type I nuclease or S1-type nucleases) includes acidic and neutral enzymes with a molecular mass between 30 and 45 kDa and that efficiently degrade RNA and denatured DNA, but not double stranded DNA. A number of Zn2+-dependent nucleases have been described in plants as, for example, the mung bean nuclease , ZEN1 from Zinnia elegans involved in tracheary element differentiation , Arabidopsis BFN1  and ENDO2 , and others . Ca2+-dependent nucleases include neutral enzymes [8, 17, 21]. For example, Arabidopsis Ca2+-dependent CAN nuclease , Eucommia ulmoides Oliv. EuCaN1 and EuCaN2 Ca2+-dependent nucleases involved in the secondary xylem development , and cucumber Ca2+-dependent nuclease CsCaN involved, among other possible functions, in the primordial anther-specific DNA damage of developing female cucumber flowers .
Determination of the catalytic requirements of a nuclease is essential for understanding its biological function. In normal conditions, plant cell nucleus and cytoplasm have a neutral pH (around 7.5) and low concentrations of Ca2+ and Zn2+, and the apoplast and vacuoles have a more acidic pH (around 5.5) . Vacuoles usually have a higher concentration of Zn2+, and apoplast a higher concentration of Ca2+ than the cytoplasm. However, this situation can change in response to different stimulus. For example, during PCD the tonoplast rupture produces a higher concentration of Zn2+ in the cytosol which also becomes more acid . It has also been reported that some stresses rise cytosolic concentration of calcium due to an increase in the Ca2+ influx from apoplasts . These changes may alter the activity of particular nucleases.
In this paper, we identify and characterize a Ca2+/Mg2+-dependent nuclease whose activity is induced by CPT in maize cultured cells. We incubated maize cells with CPT and we observed an increase in a Ca2+-dependent nuclease activity similar to what it was previously observed in maize CPT-treated embryos . This nuclease has a mass of 32 kDa, is activated by Ca2+ and Mg2+, and inhibited by Zn2+ and EDTA. It cleaves either single- and double-stranded DNA, with a higher activity against single-stranded DNA and is mainly localized in the nucleus. Two-dimensional in-gel assays and MALDI-TOF MS approaches following in-gel tryptic digestion allowed us to identify the protein responsible of the nuclease activity, which belongs to the S1/P1 type I endonuclease family.
Induction of growth arrest and DNA fragmentation by camptothecin in maize cultured cells
A nuclear-localized Ca2+/Mg2+-dependent endonucleolytic activity induced by CPT in cultured cells
The nucleases present in the cultured cells were analyzed by in-gel DNase activity assays in the presence of Ca2+ and Mg2+ (Figure 2B). An endonuclease activity with a molecular mass of 32 kDa was detected in protein extracts of treated and untreated cells, but the activity level was positively correlated with the concentration of CPT in the media. A second nuclease activity with an estimated molecular mass of 49 kDa was also observed, although its activity was much lower and did not change in response to CPT.
pH is another important factor determining nuclease activity. The majority of the plant nucleases have the highest activity at acidic or at neutral pH . We compared the intensity of the 32 kDa nuclease activity in the presence of Ca2+ and Mg2+ incubated at pH 5.5 and pH 7.5 (Figure 3A). Although the activity was also observed at pH 5.5, it was much lower than at pH 7.5. In both cases, the activity was higher in the samples extracted from CPT-treated cells.
Plant nucleases show divergent specificities towards their substrates, so, we analyzed the nucleolytic activity using single-stranded and double-stranded DNA. The 32 kDa nuclease is able to hydrolyze both single and double stranded DNA, but shows higher activity against single stranded molecules (Figure 3B). The higher affinity for single stranded DNA did not change in samples treated or not with CPT.
CaMNUC32 subcellular localization and isoforms
CaMNUC32 is a type I endonuclease of the S1/P1 family
The aim of this study was to identify possible nucleases associated with the camptothecin inhibition of cell growth in maize cultured cells. Our results revealed the existence of at least one nuclease whose activity is induced in parallel to CPT treatment. Our in gel nuclease assays demonstrated that the activity of a 32 kDa nuclease increases during CPT treatment. This activity is higher in neutral compared to acidic pH and is higher in the presence of both Ca2+ and Mg2+, whereas is reduced in the presence of the single ions. The activity is inhibited by EDTA and reduced by Zn2+. Higher nucleolytic activity was observed against ssDNA, although it is also active towards dsDNA. The nuclease activity is mainly, although not exclusively, located in the nucleus.
Bidimensional pattern of nuclease activity exhibited by CaMNUC32 suggests that this protein is subjected to post-translational modifications as it has been reported for some Ca2+-dependent nucleases , although we cannot discard that different nucleases with similar activity, size and pI exist. Heterologous expression of S1-nucleases in prokaryote systems demonstrated that post-translational events are essential for their activity [28, 30, 31]. Glycosylation is a good candidate to be responsible for the post-translational changes since the S1-nucleases and Ca2+-dependent DNases are considered to be glycoproteins [10, 29]. Nevertheless, other post-translational processes might be considered .
Ca2+/Mg2+-dependent nucleases with similar properties have been previously described in different systems. For example, rice OsCyt20 is a Ca2+/Mg2+-dependent nuclease that shows a higher activity at neutral pH and is inhibited by Zn2+. Ca2+/Mg2+-dependent nuclease has also been identified in wheat grain nucellar cells undergoing PCD and is inhibited by Zn2+. A similar nuclease of 28 kDa was observed in calf thymus chromatin . Arabidopsis CAN1 and CAN2 nucleases are neutral, Ca2+-dependent nucleases showing a different specificity toward the ssDNA, dsDNA and RNA substrates . However, the identity of the majority Ca2+/Mg2+-dependent nucleases remains uncertain .
Our 2-DE nuclease activity assay associated with spot excision and MALDI-TOF MS following in-gel tryptic digestion suggested that CaMNUC32 is a member of the S1/P1 family of type I endonucleases. Although the results provide a very limited sequence coverage (Additional file 3: Figure S3), the fact that the identified protein is a putative nuclease with a predicted molecular mass and a pI very similar to the observed ones provides enough confidence in the results. Type I S1/P1-nucleases exhibit amino acid sequence homology with nuclease S1 from Aspergillus oryzae and are classically defined by requiring Zn2+ for activation and structure stabilization, to have a pH optimum in the acidic region, to have between 30 and 43 kDa, and to be able to degrade single-stranded DNA [34, 35] although some of them have the capacity to digest both single-stranded and double-stranded DNA . Our results revealed that some S1-type nucleases are Ca2+/Mg2+dependent nucleases with neutral pH optimum. In fact, this is not the first report on a similar case. For example, the S1-like nuclease CEL1 isolated from celery was reported as a Zn2+- and Mg2+-dependent enzyme , and, recently, it has been shown that the S1-like family of nucleases in Arabidopsis, in addition to Zn2+-dependent enzymes, it also comprises nucleases activated by Ca2+ and Mn2+ and that they differ in their optimum pH value and substrate specificity . Altogether, these results reveal that plant S1-like nucleases have a surprisingly wide variety of enzyme activities. It also demonstrates that the biochemical classification of the plant nucleases does not perfectly fit their phylogenetic classification. Type I S1/P1-nuclease cannot be considered anymore as synonymous of Zn2+-dependent nuclease. The discovery of a wide variety of ions activating or inhibiting plant S1-like nucleases opens new perspectives for future research into reaction mechanisms catalyzed by these enzymes. S1-like family seems to evolve towards increasing the diversity of their catalytic properties. In fungi S1 and P1 nucleases play a role in the degradation of the extracellular DNA and RNA [37, 38], whereas in plants, most of the data suggest a relationship between S1-like nucleases and PCD. Further analyses are necessary to demonstrate that CaMNUC32 is involved in PCD. The correlation of its activity with DNA degradation suggests this function. Its mainly nuclear localization is also compatible with a role in PCD, although it is also compatible with other functions like DNA repair or recombination. CaMNUC32 activity, although at a lower extend, can be also observed in the cytoplasm, but this is not inconsistent with a PCD function. For example, the BFN1 nuclease is located in cytoplasmatic structures in early-senescent leaf cells and, as the tissue senesced, BFN1 is observed more abundantly around the nuclei . On the other hand, we also observed CaMNUC32 activity in untreated cells that may be, in principle, contradictory with a PCD function. We cannot discard that some of the cells in the culture are suffering a senescence-like process. On the other hand, nuclease activities have also been detected in tissues where PCD does not occur as, for example, in Arabidopsis mature stems which show low levels of BFN1 activity . Further analyses will be necessary to unequivocally associate CaMNUC32 with PCD.
We identified a 32 kDa nuclease, that we called CaMNUC32, whose activity is induced by the topoisomerase I inhibitor camptothecin in maize cultured cells. The activity of this nuclease is Ca2+/Mg2+-dependent and is inhibited by Zn2+ and EDTA. It cleaves either single- and double-stranded DNA. MALDI-TOF MS following in-gel tryptic digestion suggests that CaMNUC32 belongs to the S1/P1 type I endonuclease family.
Cell culture and treatments
We used the maize (Zea mays) cv Black Mexican Sweet (BMS) as a source of cultured cells. Maize cells were grown on MSE medium (MS vitamins, 20 g l-1 sucrose, 0.5 g l-1 MES, 2.4-D 2 mg ml-1, 2 g l-1 gelrite pH 5.8) and maintained at 26°C, 45% humidity and photoperiod 16/8 h. When required, the incubation medium was supplemented with camptothecin (CPT) diluted in DMSO (Sigma) and the same volume of DMSO was added to control experiments. At least three independent experiments were performed per treatment.
Isolation of DNA and agarose electrophoresis
Maize callus were frozen in liquid nitrogen and ground with a mortar and pestle. DNA was extracted with extraction buffer (100 mM Tris–HCl, pH 8.0, 50 mM EDTA, 500 mM NaCl, 10 mM β-mercaptoethanol, 2% (w/v) SDS). Contaminated RNA was removed by incubation for 10 minutes at 37°C in the presence of RNaseA (60 ng μl-1). After extraction with phenol:chloroform:isoamyl alcohol (25:24:1), DNA was precipitated with two volumes of absolute ethanol and resuspended in TE (10 mM Tris–HCl, 1 mM EDTA, pH 8.0) buffer. DNA was resolved on 1.5% (w/v) agarose gels stained with ethidium bromide.
Preparation of protein extracts
Total protein extracts were obtained from maize callus frozen in liquid nitrogen, ground with a mortar and pestle and resuspended in extraction buffer (150 mM Tris–HCl, pH 6.8, 0.5 mM PMSF, 20 μM leupeptin). The homogenate was clarified by centrifugation at 12.000x g for 5 min at 4°C. Preparation of nuclear and cytoplasmic protein extracts from maize cultured cells was done according to .
In-gel nuclease activity assay
The nuclease activity assays were carried out according to a method previously described [13, 41] with minor modifications. Protein extracts (10 μg of protein) were subjected to SDS-PAGE gels containing 50 μg ml-1 of single-stranded calf thymus DNA and 50 μg ml-1 bovine fibrinogen (Sigma). Samples were prepared in loading buffer (1% (w/v) SDS, 62.5 mM Tris–HCl, pH 6.8, 10% (v/v) glycerol, 10 mM β-mercaptoethanol) and were heated 2 min at 100°C. Electrophoresis was carried out at 20 mA and at room temperature. After electrophoresis, the gels were washed twice for 30 min in 25% (v/v) isopropanol, 10 mM Tris–HCl, pH 7.0 and then twice for 30 min in 10 mM Tris–HCl, pH 7.5. The gels were then incubated overnight at 37°C in 10 mM Tris–HCl, pH 7.5 with some of these compounds: 1 mM CaCl2, 1 mM MgCl2, 5 mM ZnSO4 and/or 1 mM EDTA. pH5.5 assays were performed in the same conditions but replacing 10 mM Tris–HCl pH 7.5 by 25 mM sodium acetate pH 5.5. Finally, the gels were stained with 1 μg ml-1 ethidium bromide for 15 min. Nuclease activity was photographed on a UV light box.
Two-dimensional nuclease activity assay
Protein extracts were resuspended in rehydration buffer (7 M urea, 2 M thiourea, 2% 3-[(3-cholamido propyl)-dimethylaminio]-1-propane sulfonate (CHAPS), 14 mM DTT, 18 mM Tris–HCl and 0.001% (w/v) bromophenol blue) and loaded onto 7 or 11 cm pH 4-7 linear IPG strips (Amersham Biosciences) for the first dimension. For nuclear extracts and dephosphorylated proteins rehydratation buffer were added by buffer exchange using Protein Desalting Spin Columns (Pierce) according to the manufacture’s method. The strips were rehydrated for 6 h at room temperature and isoelectric focusing (IEF) was performed in a IPGphor system (Amersham Biosciences) through 10 h at 50 V, 1.5 h at 500 V, 1.5 h at 1000 V, 1.5 h at 2000 v, 1.5 h at 4000 V, 2 h at 8000 V, and then holding at 8000 V until a total of at least 65000 Vh was reached. Afterwards, IPG strips were equilibrated for 15 min in equilibration buffer (50 mM Tris, pH 8.8, 6 M urea, 2% (w/v) SDS, 30% glycerol and 0.04% (w/v) bromophenol blue and then in equilibration buffer containing 10 mg-1 DTT for 15 min. Proteins were resolved in the second dimension using 10% SDS polyacrylamide gels and DNase activity assay were performed as we described above.
Western blot analysis
The extracts were subjected to SDS/PAGE (10% acrylamide). After electrophoresis, the proteins were electroblotted onto nitrocellulose membranes (Amersham Bioscience) at 0.8 mA cm-2 for 1 h using the semi-dry transfer kit (Bio-Rad). The membranes were blocked with PBS-T buffer (20 mM Tris–HCl, pH 7.5, 150 mM NaCl, 0.1% Tween-20) containing 10% (w/v) powdered milk, and proteins were immunochemically labeled by overnight incubation of the membranes at 4°C in 20 ml of PBS-T and 1:1000 Histone H3 antibody (Cell Signaling Technology®) or 1:500 polyclonal GriP mutase . Subsequent detection was performed by a chemoluminiscence assay (anti-rabbit IgG horseradish peroxidase conjugate from Roche) and SuperSignal® West Femto Maximum Sensitivity Substrate (Pearce).
Protein spots were excised from two-dimensional gels, trypsin digested and identified by ESI-Q-TOF-MS/MS. Proteins were identified either by peptide mass fingerprinting using matrix assisted laser desorption ionization-time of light mass spectrometry (MALDI-TOFMS) or by peptide sequencing. In the last case, the nanoliquid chromatography methodology coupled to nanoelectrospray tandem mass spectrometry (ESI-Q-TOF-MSMS) was carried out at the Proteomics Platform of the Barcelona Science Park. The software packages Protein Prospector v 3.4.1 (UCSF Mass Spectrometry Facility, University of California) and MASCOT were used to identify the proteins from the PMF data. The SEQUEST software (Thermo-Instruments, Spain) was used for preliminary protein identification from the tandem mass spectra analysis followed by manual sequence data confirmation. Sequence searching was performed on UniProtKB/Swiss-Prot protein knowledgebase and NCBInr databases 20050416 (2.440.549 sequences; 825.977.590 residues) and 20060729 (3.822.560 sequences; 1.317.468.070 residues) using protein full range of Mr and pI. No taxonomy restriction was applied. We used the following parameters for the searches: 1 missed cleavage; fixed and variable modifications were carbamidomethyl of cystein and oxidation of methionine, respectively. The peptide mass and fragment tolerance were 200 ppm and 0.25 Da, respectively. For MASCOT searching, individual ion scores >47 indicated identity or extensive homology (p < 0.05).
We thank Dr. F.J Cejudo (IBVF-CSIC, Sevilla, Spain) as a host for an NSP short termed stay. We also thank Dr P. Fontanet (CRAG, Barcelona, Spain) for maize cell culturing support, and Drs. D. Ludevid and Dr. M. Riera (CRAG, Barcelona, Spain) for providing the polyclonal anti-GriP mutase and anti-Rab17 antibodies, respectively. This work was supported by grants BIO2004-01577 and AGL2009-09151 from Plan Nacional de Investigación Científica y Técnica (Ministerio de Ciencia y Tecnología, Spain), by the Centre CONSOLIDER on Agrigenomics and by the Xarxa de Referencia en Biotecnologia of the Generalitat de Catalunya. NSP was supported by a grant from the Consejo Superior de Investigaciones Científicas (CSIC). This publication was supported by the Unit of Information Resources for Research (CSIC).
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