Comparative proteomic analyses of Asian cotton ovules with attached fibers in the early stages of fiber elongation process
© The Author(s). 2016
Received: 22 March 2016
Accepted: 1 September 2016
Published: 8 September 2016
Plenty of proteomic studies were performed to characterize the allotetraploid upland cotton fiber elongation process, whereas little is known about the elongating diploid cotton fiber proteome.
In this study, we used a two-dimensional electrophoresis-based comparative proteomic approach to profile dynamic proteomes of diploid Asian cotton ovules with attached fibers in the early stages of fiber elongation process. One-way ANOVA and Student-Newman-Keuls test were used to find the differentially displayed protein (DDP) spots.
A total of 55 protein spots were found having different abundance ranging from 1 to 9 days post-anthesis (DPA) in a two-day interval. These 55 DDP spots were all successfully identified using high-resolution mass spectrometric analyses. Gene ontology analyses revealed that proteoforms involved in energy/carbohydrate metabolism, redox homeostasis, and protein metabolism are the most abundant. In addition, orthologues of the 13 DDP spots were also found in differential proteome of allotetraploid elongating cotton fibers, suggesting their possible essential roles in fiber elongation process.
Our results not only revealed the dynamic proteome change of diploid Asian cotton fiber and ovule during early stages of fiber elongation process but also provided valuable resource for future studies on the molecular mechanism how the polyploidization improves the trait of fiber length.
KeywordsAsian cotton Ovule Fiber elongation Differentially displayed protein spots Polyploidization
As a major source of natural fiber in the world, cotton has been widely used for clothing, papermaking, and other purposes for thousands of years . Apart from its economic value, cotton is also known as an excellent model system for studying cell differentiation, cell elongation and cellulose biosynthesis . All cotton plants belong to the genus Gossypium in the family Malvaceae. Among the around 50 known Gossypium species, only four cultivated species, G. arboreum, G. herbaceum, G. hirsutum, and G. barbadense, can produce spinnable fibers. The first two cultivated species are diploids (AA) and the last two are allotetraploids (AADD) originating by a polyploidization event involving G. herbaceum and a diploid hairiness species resembling G. raimondii (DD) . Interestingly, the fiber length of the two allotetraploids species are longer than the two diploids species. Considering that the progenitor DD genome species are fiber deficient, the long-fiber phenotype of allotetraploid cotton species must be formed in the polyploidization process through some unknown complex mechanism [4–6]. Elucidation of the molecular mechanism of fiber elongation in the diploid cotton and further comparison of the differences of fiber elongation between the diploid and allotetraploid cotton could help us understand how the polyploidization improves the traits of fiber length .
With the availability of high-quality EST sequences in public databases, high-throughput proteomic analyses of cotton fiber elongation process were successfully performed in advance of the cotton genome sequencing project. For example, a proteomic study of the ligon lintless mutant and wild-type upland cotton fibers identified 81 differentially displayed protein (DDP) spots at 14 days post-anthesis (DPA), suggesting that proteins involved in protein folding and stabilization are important for fiber elongation . Another study that compared the proteomic profiles of wild-type and fuzzless-lintless mutant upland cotton (G. hirsutum cultivar Xu142) fibers at 10 DPA identified 104 DDP spots, providing evidence that pectin synthesis is imperative for fiber elongation . In another 2-DE-based comparative proteomic analysis, a total of 235 protein spots were found having different abundance during the entire elongation process at five distinct time points: 5, 10, 15, 20 and 25 DPA of upland cotton (G. hirsutum cultivar CRI 35) . Further Kyoto Encyclopedia of Genes and Genomes (KEGG) Orthology-based Annotation System (KOBAS) analyses based on the identified 235 DDPs indicated that glycolysis is the most significantly regulated biochemical pathway during the fiber elongation process . With the availability of cotton genome sequences, post-genomic proteomics studies further shed many new insights into cotton fiber initiation and elongation processes [12–16]. Hu et al. successfully compared the total proteome of two allotetraploid cotton species (G. hirsutum and G. barbadense) and their diploid parents at 10 and 20 DPA, providing the first evidence that the two allopolyploid species have achieved superficially similar modern fiber phenotypes through different evolutionary routes . However, the mechanisms of which proteins are essential for fiber elongation and how polyploidization increases the fiber length of the allotetraploid upland cotton are poorly understood. Furthermore, because most of these proteomic studies focused on the midst and late stage of fiber elongation process, the early events occur in the fiber elongation process are still poorly characterized at the proteome level.
In the present study, we reported the first comparative proteomic analyses of fiber and ovule proteome of diploid Asian cotton (G. arboreum cultivar DPL971) in the early stages of elongation process (1-9 DPA) and the identification of 55 DDPs of developing diploid cotton ovules with attached fibers. Through comparing the dynamic proteome of Asian cotton ovules and attached fibers with differential proteome of upland cotton fibers, we clarified 13 possible essential proteins required for fiber elongation and four important proteins whose increased abundance are correlated with improved fiber length.
Results and discussions
Dynamic proteomes of diploid Asian cotton ovules and fibers in the early stages of fiber elongation process
Fiber length measurement indicated that the diploid Asian cotton (G. arboreum cultivar DPL971) shows a gradual increase of fiber length during the early stages of fiber elongation process as the allotetraploid upland cotton (G. hirsutum cultivar CRI35) does (Additional file 1: Figure S1). The fastest fiber elongation rate was observed at 5 DPA in both two cultivars. Since then, the elongation rate gradually slowed down. Interestingly, the fiber length of cultivar DPL971 is always shorter than that of cultivar CRI35 (Additional file 1: Figure S1), supporting the notion that polyploidization improves the fiber length trait.
Functional analyses of the differentially displayed proteins of diploid Asian cotton ovules and fibers in the early stages of fiber elongation process
Many of the 55 DDPs were known important proteins required for proper fiber initiation and elongation. For example, DDP No. 31 and 39 were identified as two different Cu/Zn superoxide dismutase, which was previously characterized to be important for cotton fiber development . Similarly, DDP No. 14, 40 and 54 were all identified as ATP synthase subunits, which was previously proved playing vital roles in cotton fiber elongation process . The activity of malate dehydrogenase (DDP No.34) is variant among cotton cultivars with differing fiber traits , whereas chalcone synthase (DDP No.24 and 53) and dihydroflavonol 4-reductase (DDP No.16), two important enzymes involved in flavonoid metabolism, were reported being related to cotton fiber quality [23, 24].
Furthermore, although the function of some DDPs are unclear in cotton, investigation of the gene homologs in model plant Arabidopsis also implied their important functions in ovule and fiber development. For example, DDP No. 06 was identified as a thiosulfate sulfurtransferase, which plays important roles in embryo and seed development in Arabidopsis thaliana . DDP No. 33 was identified as a dihydrolipoamide dehydrogenase, the E3 subunit of pyruvate dehydrogenase complex. In Arabidopsis thaliana, mutations of plastid pyruvate dehydrogenase complex will lead to an early embryo lethal phenotype, suggesting the important function of pyruvate dehydrogenase complex in embryo development . During fiber development process, the fiber cells are always attached with the ovules which provide the fiber cells essential water, carbon source and mineral nutrients . Identification of the important proteins required for embryo/ovule development in this study could give us the clue how the cotton plants delicately regulate the complex sink and source relationship of ovule and fiber to promote the fast elongation of fiber cells. This important information couldn’t be obtained through studies only focusing on fibers.
Comparative analyses of the differentially displayed proteins of diploid Asian cotton ovules and fibers with allotetraploid upland cotton fibers
Blast search indicated that 13 of the 55 DDPs of diploid Asian cotton ovules with attached fibers in early stages of fiber elongation process were also identified in the comparative proteomic analyses of the elongating allotetraploid upland cotton fiber cells [10, 11], suggesting these 13 DDPs are required for fiber elongation (Fig. 4b). Moreover, nine of the 13 DDPs were found having more copies in allotetraploid upland cotton fiber cells than in diploid Asian cotton fiber/ovule cells (Fig. 4c). Notably, the different copies of the selected DDPs in allotetraploid upland cotton all have the same protein sequence, suggesting these different proteoforms are differentially post-translationally modified. For example, four DDPs of phospholipase D alpha protein were identified in allotetraploid fiber with the same NCBI accession number whereas only one DDP was identified in diploid fiber/ovule.
Comparison of the protein abundance between the 13 DDPs in diploid Asian cotton and the homologous 29 DDPs in allotetraploid upland cotton at 5 DPA, the same time point of fiber elongation process, further revealed that protein abundance of four proteins, including translation initiation factor, actin, isocitrate dehydrogenase and phosphoglycerate mutase, were all increased in allotetraploid upland cotton (Fig. 4c). Moreover, DDP number of the four proteins were also increased in allotetraploid upland cotton. These results strongly suggested that activity of the four proteins might be selectively up-regulated in the polyploidization process, implying the four proteins are important for improving the fiber length trait. In agreement with this suspicion, fiber length of the transgenic cottons expressing the actin gene is significantly longer than that of wild-type cotton plants .
In summary, we reported the first comparative proteomics study of diploid Asian cotton ovules with attached fibers in the early stages of fiber elongation process. Combined with the proteome dataset of elongating allotetraploid upland cotton fibers, our study provides a reference list of essential proteins supporting the fast cotton fiber elongation process. Information of these essential proteins including protein expression level and MS identification data provide a valuable resource for future functional studies.
Asian cotton (G. arboreum cultivar DPL971) and upland cotton (G. hirsutum cultivar CRI35) was grown in a standard agronomic field during the period from April to September in Beijing. The ages of the ovules with attached fibers selected for total protein extraction and fiber length measurement were 1, 3, 5, 7 and 9 DPA. All of the collected samples were frozen in liquid nitrogen and then stored at −80 °C for protein extraction.
Measurements of fiber length
Ovules were detached from the fresh cotton bolls and boiled at 95 °C water bath for 10 min. Aggregated fibers were combed in water, observed and photographed under a SZX12 anatomy microscope (Olympus, Japan) equipped with a DP70 digital camera system. Five ovules were used to represent each developmental stage whereas length of 10 fibers were recorded for each ovule.
Total protein was extracted using modified Tris-phenol method as described . About 1 g of frozen cotton ovules with attached fibers was ground with 10 % PVPP (w/w) and 10 % quartz sand (w/w) in liquid nitrogen using a mortar and pestle. The powder was suspended completely in twenty milliliters of ice-cold acetone (adding 2 % β-mercaptoethanol) and centrifuged at 12,000 g for 15 min at 4 °C to wash away impurities, and this step was repeated twice. The freeze-dried powder was homogenized in 5 mL of extraction buffer containing 50 mM Tris–HCl, pH 8.6, 2 % SDS, 2 % (w/w) β-mercaptoethanol, 1 mM PMSF, and then an equal volume of Tris saturated phenol (pH 8.0) was added. The mixture was vortexed thoroughly for 5 min, and the phenol phase was collected and precipitated with 5 volume of 0.1 M ammonium acetate in methanol at −20 °C for 30 min. After centrifuging at 12, 000 g for 15 min, the collected protein pellets were washed three times with cold 0.1 M ammonium acetate in methanol, and then washed three times with cold 80 % acetone in water. The lyophilized pellets were dissolved in rehydration buffer (7 M urea, 2 M thiourea, 4 % CHAPS, 1 % IPG buffer, 20 mM DTT) and centrifuged at 12 000 g for 15 min to remove insoluble materials. The concentration of extracted proteins was quantified using Bradford method with biotechnology grade BSA protein as a quantification standard . The proteins underwent 2-DE immediately or were stored at −80 °C.
2-DE and image analyses
2-DE was performed according to the manufacturer’s instruction (2-DE Manual, GE Healthcare). 1 mg protein mixed with rehydration buffer (7 M urea, 2 M thiourea, 4 % CHAPS, 1 % IPG buffer, 20 mM DTT) in a total volume of 1 mL, was loaded onto a nonlinear IPG Drystrip (pH 3-10, 24 cm, GE Healthcare, Piscataway, USA). The strips were hydrated in the rehydration buffer for 18 h at room temperature. Then isoelectric focusing was performed on an Ettan IPGphor isoelectric focusing system (GE Healthcare, Uppsala, Sweden) under the following conditions: 100 V for 40 min, 500 V for 40 min, 1000 V for 1 h, 4000 V for 2 h, and 8000 V for 8 h until total voltage hours of 75,000 was achieved. Before SDS-PAGE analysis, strips were incubated for 2 × 15 min in equilibration buffer (6 M urea, 50 mM pH 8.8 Tris–HCl, 30 % (v/v) glycerol, 2 % (w/v) SDS, a trace of bromophenol blue). One percent DTT (w/v) was added to the above for the first 15 min and 2.5 % iodoacetamide (w/v) instead for the second 15 min. After equilibration, strips were placed on top of a vertical 12.5 % SDS-polyacrylamide self-cast gel and electrophoresis was performed at 4 °C and 5 W/gel for 45 min, and then 17 W/gel for 5 h until the dye front reached the bottom of gels. For calculation of molecular weight (MW) of the 2-DE protein spots, a filter paper piece pre-loaded with a protein marker (14.4–97.4 kDa) were placed along with the equilibrated strip on top of the gels. After electrophoresis, 2-D gels were stained by Colloidal Coomassie Blue G-250 . The 2-D gels were scanned at 600 dpi resolution using a UMAX PowerLook 2100XL scanner (Willich, Germany) with following parameters: scan mode, transparent; color, grey; calibration, auto calibration. Image analysis was performed with ImageMaster Platinum software (version 6.0) (GE Healthcare). Proteins extracted from three different samples of each time point were analyzed by 2-DE and triplicates were applied to each protein sample, thus a total of 45 CBB-stained 2-D gel images were obtained. The spots were quantified using the % volume criterion. The match analysis was done in automatic mode using the following detection parameters: Smooth 4, Saliency 300, and Min Area 29, and further manual editing was performed to correct the mismatched and unmatched spots. The relative volume of each spot was assumed to represent its expression abundance. A significant difference was defined by the criterion p-value < 0.05 when analyzing parallel spots between groups with one-way ANOVA and Student-Newman-Keuls test using the SPSS 16.0 statistical software (IBM).
Protein identification by MALDI-TOF/TOF
Protein spots were manually excised from the 2-D gels and digested with trypsin. Briefly, the excised gel pieces were destained with 100 mL of 25 mM NH4HCO3 in 50 % ACN until the stain faded sufficiently. After that, the gel pieces were washed twice in 100 % ACN for 10 min and then dried under vacuum for 15 min. Proteins in the gel pieces were digested in 25 mM NH4HCO3, 10 ng/mL trypsin overnight at 37C. The digestion solutions were used in the subsequent MS analysis. The 4800 MALDI TOF/TOF™ Analyzer (Applied Biosystems, Framingham, USA) was used for protein identification. The MS spectra were acquired in the positive ion reflector mode, with a mass range from 800 to 4000 Da. The peaks with S/N > 20 were selected for PMF analysis. The MS/MS analysis was performed with the 10 strongest peaks of the MS spectra, and the precursor ions were accelerated at a voltage of 8 kV. The MS/MS spectra were accumulated for at least 2000 laser shots. All of the MS and MS/MS data were analyzed in the combined mode using Global Proteome Server Explorer (software version 3.5, Applied Biosystems) to interface with the Mascot 2.2 search engine (Matrix Science) against a G. arboreum peptide sequence database downloaded from Cotton Genome Project website (http://cgp.genomics.org.cn, including 41,331 protein sequences, 14,876,209 residues) . Searching parameters were set as follows: S/N ≥ 3.0; fixed modification, carbamidomethyl (Cys); variable modification, oxidation (Met); maximum number of missing cleavages, 1; MS tolerance, ± 0.1 Da; MS/MS tolerance, ± 0.5 Da. The identities with the highest score were subsequently analyzed using blast tools against the Uniprot database (http://www.uniprot.org/) to obtain the gene ontology (GO) annotation.
Antibody preparation and western blot
The specific antibodies against selected proteins, chloroplast Cu/Zn superoxide dismutase (ChSOD) and heat shock protein 70 (HSP70), were prepared by the immunisation of rabbits with synthesised protein-specific peptides (MAAHIFTTTPSHL for ChSOD and RSFRRRDIAASPL for HSP70) mixed with Freund adjuvant by Beijing Protein Innovation (Beijing, China). Affinity purifications were further performed to enrich antibodies to ensure the titers against synthesised protein-specific peptides larger than 1: 6400 by ELISA. Goat anti-rabbit antibodies that were conjugated to horseradish peroxidase were used as secondary antibodies. For western blotting, 20 μg of proteins for each sample were denatured in 6 × SDS-PAGE sampling buffer by boiling in a water bath for 5 min, then separated by 12 % SDS-PAGE along with a pre-stained protein marker (10–124 kDa) and transferred to a PVDF membrane. The signals were revealed with Lumi-Light western blotting substrate (Roche, Mannheim, Germany) and captured on autoradiographic films (Kodak, New York, USA). Films were scanned using UMAX PowerLook 2100XL scanner and densitometric analysis of the bands was performed using ImageMaster Platinum software. The experiments were repeated for three times using different ovule attached with fiber samples.
Bioinformatics analyses of the differentially displayed protein spots
A complete linkage hierarchical cluster analysis of the differentially displayed protein (DDP) spots was performed through a comparison of the average fold change value of each spots (comparison to 1 DPA) using MeV 4.7 software package. Functional classification of the DDP spots were performed using agriGO toolkits (http://bioinfo.cau.edu.cn/agriGO/) in hypergeometric testing mode. Amino acid sequences of the DDP spots were BLAST searched against with known DDPs of allotetraploid elongating cotton fibers to retrieve the most homologous allotetraploid cotton DDPs with an E-value = 0.
Chloroplast Cu/Zn superoxide dismutase
Differentially displayed protein
Expressed sequence tag
Heat shock protein 70
- MALDI TOF:
Matrix-assisted laser desorption/ionization time of flight
Peptide mass fingerprinting
The authors want to thank the five anonymous reviewers for providing constructive comments on the manuscript.
This work was supported by grants from the State Key Basic Research and Development Plan (2010CB126003), the National Natural Science Foundation of China (90608016), the National Transgenic Animals and Plants Research Project (2011ZX08009-003) and State Key Laboratory of Cotton Biology Open Fund (CB2015A01). The funding bodies do not have a role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Availability of data and materials
All data generated or analysed during this study are included in this published article and its supplementary information files.
JL designed the study and helped to draft the manuscript; BZ conceived the study, participated in its design and drafted the manuscript; SD and JH performed 2-DE; DM carried out MS analysis and performed protein identification. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
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