Genome-wide expression analysis of reactive oxygen species gene network in Mizuna plants grown in long-term spaceflight
- Manabu Sugimoto†1Email author,
- Youko Oono†2,
- Oleg Gusev3, 4, 2,
- Takashi Matsumoto2, 5,
- Takayuki Yazawa6,
- Margarita A Levinskikh7,
- Vladimir N Sychev7,
- Gail E Bingham8,
- Raymond Wheeler9 and
- Mary Hummerick9
© Sugimoto et al.; licensee BioMed Central Ltd. 2014
Received: 13 September 2013
Accepted: 31 December 2013
Published: 6 January 2014
Spaceflight environment have been shown to generate reactive oxygen species (ROS) and induce oxidative stress in plants, but little is known about the gene expression of the ROS gene network in plants grown in long-term spaceflight. The molecular response and adaptation to the spaceflight environment of Mizuna plants harvested after 27 days of cultivation onboard the International Space Station (ISS) were measured using genome-wide mRNA expression analysis (mRNA-Seq).
Total reads of transcripts from the Mizuna grown in the ISS as well as on the ground by mRNA-Seq showed 8,258 and 14,170 transcripts up-regulated and down-regulated, respectively, in the space-grown Mizuna when compared with those from the ground-grown Mizuna. A total of 20 in 32 ROS oxidative marker genes were up-regulated, including high expression of four hallmarks, and preferentially expressed genes associated with ROS-scavenging including thioredoxin, glutaredoxin, and alternative oxidase genes. In the transcription factors of the ROS gene network, MEKK1-MKK4-MPK3, OXI1-MKK4-MPK3, and OXI1-MPK3 of MAP cascades, induction of WRKY22 by MEKK1-MKK4-MPK3 cascade, induction of WRKY25 and repression of Zat7 by Zat12 were suggested. RbohD and RbohF genes were up-regulated preferentially in NADPH oxidase genes, which produce ROS.
This large-scale transcriptome analysis revealed that the spaceflight environment induced oxidative stress and the ROS gene network activation in the space-grown Mizuna. Among transcripts altered in expression by space conditions, some were common genes response to abiotic and biotic stress. Furthermore, certain genes were exclusively up-regulated in Mizuna grown on the ISS. Surprisingly, Mizuna grew in space normally, as well as on the ground, demonstrating that plants can acclimate to long-term exposure in the spaceflight environment by reprogramming the expression of the ROS gene network.
KeywordsmRNA-Seq Next generation sequencing Transcriptome Mizuna Reactive oxygen species International Space Station Spaceflight
Plant cultivation in space will be necessary to augment stored foods when space mission distances and durations increase, such as for long term bases on the Moon and Mars, and even being considered for orbiting bases such as the International Space Station (ISS). Plants can play an important role in supplying nutrients, oxygen, and water to humans and can be co-utilized for waste recycling in space [1, 2], therefore, establishment of the culture approaches and breeding/developing plants to optimize their performance in space will be critical to future advanced space life support systems. In space, plants can be exposed to unusual and extreme environments, such as space radiation, reduced gravity, reduced atmospheric pressure, elevated or super-elevated CO2 concentrations, and temperature excursions. In orbital, spaceflight cabin, lunar and Martian bases, environmental conditions for plant cultivation such as temperature, light, air, and water could be controlled, however, it would be hard to eliminate space radiation and reduced gravity, which are suspected to perturb plant growth and development.
Space radiation and microgravity are suggested to generate reactive oxygen species (ROS) in plants. Ionizing radiation produced ROS  and increased lipid peroxidation products in erythrocytes of mice housed for about 100 days in ISS , and exposure of Arabidopsis seedlings and callus cells to altered gravitational forces (clinorotation or hyper gravity) up-regulated genes associated with cellular signaling, protein phosphorylation/dephosphorylation, defense, stress response, and gravisensing [5–7]. Gene expression profiles have been analyzed to understand the stress level and adaptation challenges in plants grown in space. Arabidopsis plants (7 days old) launched and grown for 5 days in the Space Shuttle showed that the genes of HSP, drought-inducible calcium binding protein, a MADS-box protein, and MAP kinases were induced 4-fold, compared with those of ground control . Pathogen response, wounding, drought, and cold associated genes, a gene associated with auxin-mediated lateral root development, and an essential regulator gene of photorespiration were up-regulated more than five-fold in the Arabidopsis seedlings, which were germinated and grown for 12 days in the Space Shuttle. In addition, genes associated heat shock, salt, drought, metals, wounding, phosphate, ethylene, senescence, terpenoids, seed development, cell walls, photosynthesis, and auxin were up-regulated by more than five-fold in the culture cells grown for 12 days in the Space Shuttle . These results indicate that plant genes in the ROS network, which are induced by abiotic and biotic stress [10, 11], can be triggered by changes related to the spaceflight environment. However, because of the limitation of launching and cultivation in space, few studies on gene expression profiles have been performed, and in many cases plant materials were transported to orbit (i.e., not grown entirely in spaceflight), subjecting them to transient responses that may not have been due to spaceflight environment.
We have developed a plant growth system, namely Lada, which was installed in ISS to study and grow plants, including vegetables in a spaceflight environment. We have succeeded in cultivating Mizuna, tomato, pea, radish, wheat, rice, and barley in Lada aboard ISS. Both M1 and M2 pea grown from seeds formed during spaceflight showed no significant difference in growth, developmental characteristics, frequency of chromosome aberrations in primary root meristem, and level of molecular polymorphism between offspring of space-grown and ground control seeds . On the other hand, transcription levels of superoxide dismutase, glutamyl transferase, catalase, and ascorbate peroxidase were increased in the barley germinated and grown for 26 days in Lada, though the whole-plant growth and development of the barley in spaceflight were the same as in the ground control barley . These results suggest that plants can adapt to spaceflight environment by changing their ROS gene network.
In this study, we investigated the response of the ROS gene network in Mizuna, Brassica rapa var. nipposinica, cultivated for 27 days in ISS. Mizuna is one of the model plants for cultivating in Lada aboard ISS because it is a leafy vegetable that can fully develop in 4 weeks in order to supply not only a plant material for investigating the effect of spaceflight environment but also a fresh vegetable for astronauts to take nutrient and benefit mental health quickly . The ROS gene network consists of a vast numbers genes, therefore, large-scale transcriptome analysis is necessary to clarify the stress level and adaptation challenges in plants under the spaceflight environment. The mRNA-Seq strategy using next generation sequencing (NGS) technology has become a powerful tool for analyzing genome-wide gene expression and global transcriptional networks. mRNA-Seq overcomes the limitations of microarray analysis, of which the probes are designed on the basis of a reference genome sequence of model species and cover only small portion of a gene. We demonstrated that an overall gene expression of the ROS gene network in the space-grown Mizuna was characterized by mapping reads from the NGS analysis to the Brassica database as a reference genome sequence and annotating genes. Our results provide a survey of plant response to the spaceflight environment and define common and different genes and cascades in the ROS gene network for adapting to the spaceflight environment.
Results and discussion
Growth of Mizuna in space
The seeds of Mizuna was transported to ISS, germinated, and grown in “Lada”, plant growth chamber aboard the Russian segment of ISS, which has successfully produced a harvest of fresh vegetables and seeds in space [12, 14, 15]. The fresh weight and water content of the space-grown Mizuna were 82.9 g and 92.5%, and those of the ground-grown Mizuna were 58.0 g and 92.0%, respectively, after 28 days of cultivation, showing that Mizuna grew as well or better under spaceflight environment in ISS as well as on the ground. The reduced growth of the ground controls was likely due to the close matching of watering protocols for space and ground plants, which resulted in slower germination on the ground and some wilting symptoms of some ground control plants just prior to harvest. Although similar amounts of water were being added to space and ground plants, the tendency of water to settle to the bottom of the root trays on the ground (and be more uniformly distributed in space) could have affected overall growth.
Construction of the Mizuna transcript dataset and identification of differentially expressed transcripts
Total reads of transcripts from the space-grown and the ground-grown Mizuna by paired-end sequencing assay were 73,028,136 and 74,578,954. Also, 44,994,328 (61.6%) and 49,195,408 (66.0%) of transcripts of total reads were mapped to the reference Brassica rapa genome sequence, respectively. A G-test [false discovery rate (FDR) < 0.001] was performed on the read count of transcripts to detect differences in gene expression between the space-grown and the ground-grown Mizuna, and to identify responsive transcripts of the space-grown Mizuna. The numbers of up-regulated and down-regulated transcripts were 8,258 and 14,170, which respectively included 467 and 1,208 unannotated transcripts (Additional file 1: Table S1).
Expression profiles of oxidative marker and ROS-scavenging genes
Expression of oxidative marker genes in the space-grown Mizuna
Trypsin inhibitor, putative
Disease resistance protein putative
DNAJ heat shock
Glutathione S-transferase, putative
WRKY family transcription factor
Glutathione S-transferase, putative
Glutathione S-transferase, putative
Armadillo/beta-catenin repeat family protein
UDP-glucosyl transferase family protein
UDP-glucosyl transferase family protein
Cell division cycle protein 48, putative
FAD-binding domain-containing protein
UDP-glucosyl transferase family protein
Mannitol dehydrogenase, putative (ELI3-2)
WRKY family transcription factor
FAD-binding domain-containing protein
Cytochrome P450 71B15, putative
Cytochrome P450, putative
bHLH transcription factor
Zinc finger (AN1-like) family protein
Glutathione S-transferase, putative
ROS-scavenging genes are induced to defend the cells from oxidative stress. The expression level of transcripts associated with Arabidopsis ROS-scavenging genes  was confirmed in the space-grown Mizuna (Additional file 3: Table S3). In fact, 20 transcripts were up-regulated more than two-fold, including the major ROS-scavenging enzymes: superoxide dismutase, catalase, and glutathione peroxidase. A dramatic induction occurred in thioredoxin (Bra014037) and glutaredoxin (Bra030102, Bra032911) genes, of which the levels were increased more than 40-fold. Thioredoxin and glutaredoxin belong to the thioredoxin superfamily known to be crucial for maintaining a reduced intracellular redox state and oxidative defense . Alternative oxidase (AOX) (Bra010153) was another highly expressed gene, with 9.2-fold up-regulation. AOX activity increases in plants under oxidative stress such as drought and salinity, and AOX functions as an antioxidant enzyme, acting to alleviate ROS accumulation [20–22]. These results suggest that the Mizuna modulates ROS-scavenging genes to eliminate oxidative stress induced by the spaceflight environment.
Expression profiles of ROS-responsive transcription factor genes
Expression of ROS-responsive transcription factor genes in the space- grown Mizuna
Expression profiles of ROS-producing genes
Expression of NADPH oxidase genes in the space-grown Mizuna
NADPH oxidase (RbohA)
NADPH oxidase (RbohB)
NADPH oxidase (RbohC)
NADPH oxidase (RbohD)
NADPH oxidase (RbohE)
NADPH oxidase (RbohF)
NADPH oxidase (RbohG)
NADPH oxidase (RbohH)
NADPH oxidase (RbohI)
NADPH oxidase (RbohJ)
Plants respond to environmental stress in multiple ways and have evolved mechanisms to increase their tolerance to the stress through interactive molecular and cellular changes. The components of these changes are responses of integrated ROS gene network triggered under stressful conditions. Our large-scale transcriptome analysis demonstrated that the spaceflight environment induced oxidative stress and activated a ROS gene network in the space-grown Mizuna, some of which were common genes up-regulated by abiotic and biotic stress and some of which were preferentially up-regulated genes by the spaceflight environment, even though Mizuna grew in the space as well as on the ground. Up-regulation of AOX, RbohD, and RbohF genes, activation of more than one MAPK cascades, and regulation of Zat7 and WRKY70 by Zat12 are common in plants under space, abiotic, biotic stress. Preferential high expression of thioredoxin and glutaredoxin genes, no repression of WRKY25, WRKY33, and Zat12 by MEKK1-MKK1/MKK2-MPK4 cascade, and no induction of OXI1 by PLC/D-PA-PDK1 pathway are different from those under abiotic and biotic stress. These results show that the ROS gene network for abiotic and biotic stress response and tolerance, which plants have developed to adapt the environment on the earth, could serve to acclimate plant to the abiotic stress conditions of the spaceflight environment.
Plant cultivation and spaceflight
Seeds of Mizuna, Brassica rapa var. nipposinica, were transported to ISS. Ten-15 seeds were set in each of two root modules of the Lada growth chambers aboard the Zvezda module of ISS [14, 15], and allowed to germinate. Lada consists of a control module, a water reservoir and 2 growth chambers which include a root module, leaf chamber and light module (Additional file 6: Figure S2). The light banks house two cool white flourescent lamps providing approximately 125-250 μmol m-2 s-1 (depending on plant height) photosynthetically active radiation (PAR). In the overall Lada experiment, two root module growth substrate mixtures were used to determine which was optimal for plant growth. One mixture contained rinsed and dried arcillite (Turface Proleague, Profile LLC, Buffalo Grove IL, US) with 15 grams of 14-14-14 Osmocote fertilizer, the other, nutrient solution soaked and dried arcillite with 14 grams of a custom mixed Nutricote fertilizer. The Lada moisture level control point was set at 85% at the start of the experiment for both root modules. One of the root modules experienced an over-watering event in which the pump failed to stop when the moisture sensors reached 85% and almost 2 liters of water was added in 35 hours. Automatic watering was disabled and the pump was operated manually for the duration of the experiment. This was duplicated in the ground controls. Because of the difference in watering regimes, only the plant tissue from the Osmocote fertilized root modules with manually controlled watering, both flight and ground controls, were used for this study. The plants were grown in Lada under 24 hr lighting. The average environmental conditions measured from the Zvezda module of the ISS over the duration of the experiment and duplicated for the ground controls were 24.3 ± 0.8°C, 3.27 ± 0.46 mm Hg pp CO2, (= 4,303 ± 605 ppm CO2) and 40.7 ± 6.9% RH. The average recorded values for the ground control experiment were 24.5 ± 0.5°C, 4,254 ± 566 ppm CO2, and 41.2 ± 2.6 RH. After 27 days of cultivation, the plants were harvested and stored at -80°C in the MELFI freezer onboard the Destiny module, and were transported to the ground at < -20°C in the GLACIER cold stowage system aboard the Space Shuttle. The total radiation dose during cultivation was 8.37 mGy.
RNA preparation, mRNA-Seq analysis and identification of responsive transcripts
Total RNA from leaves samples was extracted using the RNeasy Plant Mini kit (Qiagen, Hilden, Germany) and cDNA library was constructed using the TruSeqTM RNA sample preparation kit (Illumina, San Diego, CA, USA). Sequencing was performed on each library to generate 100-bp paired-end reads for transcriptome sequencing on Illumina Genome Analyzer IIx platform. Stretches of low quality bases at both sides of reads were trimmed using a customized C program (Q value < 15). Adapter sequences were removed using cutadapt (ver. 1.0; http://code.google.com/p/cutadapt/) with parameters ‘-e 0.1 -O 5 -m 20’ . After pre-processing the Illumina reads, the transcript structures were reconstructed using a series of programs, namely, Bowtie 2 (ver. 2-2.0.0-beta7; http://bowtie-bio.sourceforge.net/bowtie2/index.shtml) for short-read mapping , TopHat (ver. 2.0.5; http://tophat.cbcb.umd.edu/) for defining exon-intron junctions , and Cufflinks (ver. 2.0.2; http://cufflinks.cbcb.umd.edu/) for gene structure predictions . For TopHat, the Reference-Brassica rapa (Chiifu-401) genome (Phytozome; http://www.phytozome.net/) was used as the reference sequences with the following options: --no-discordant --no-mixed -r 46 --mate-std-dev 133 .
The expression level for each transcript was calculated as reads per kilobase of exon model per million mapped (RPKM) values based on the number of uniquely mapped reads that completely overlap with the exonic regions in each library . The significantly differentially expressed transcripts between space- and ground-grown samples were detected by G-test (FDR < 0.001). Fold changes of expression levels between samples were calculated after adding one to each RPKM value to avoid division by zero.
Gene ontology analysis
The GO terms assigned to the responsive transcripts were obtained from InterProScan 5 Release Candidate 2 (http://code.google.com/p/interproscan/) with the parameters ‘-f tsv -t p -dp –goterms’ for each transcript .
GO enrichment analysis
GO enrichment was evaluated for responsive transcripts using Fischer’s exact test with a FDR threshold of 5% using R ver. 2.13.0 (http://www.r-project.org).
Quantitative RT-PCR (qRT-PCR)
Poly(A)+ RNA was purified from total RNA with the Poly (A) Purist MAG (Ambion, Texas, USA) and 1st strand cDNA was synthesized from poly(A)+ RNA with the PrimeScript first strand cDNA Synthesis Kit (Takara Bio, Japan) according to the manufacture’s instruction. qRT-PCR was performed in a mixture of 10 μl containing 1st strand cDNA, SYBR Premix Ex Taq (Takara Bio, Japan), and 0.2 μmol each primer combination (Additional file 5: Table S4) using the LightCycler 2.0 (Roche Applied Science, Mannheim, Germany). The thermal cycle profile was 1cycle of 95˚C for 10 sec followed by 40 cycles of 95˚C for 5 sec, 60˚C for 20 sec. The cDNA quantities of each gene were calculated using LightCycler 4.0 software and the transcript expression levels were normalized with that of the α-tubulin gene as an internal control. Three technical replicate for each RNA were used for analysis. Specificity of primer combination was confirmed by melting curve of the PCR products and agarose gel electrophoresis (Additional file 4: Figure S1).
The resulting mRNA-Seq data were deposited in the DDBJ Sequence Read Archive (http://trace.ddbj.nig.ac.jp/dra/index_e.html) under the accession No. DRA001106.
We thank Russian and American astronauts for perfect operator activity of this series of plant cultivation in ISS and transportation. This research was supported in part by the Ohara Foundation of Kurashiki, Japan.
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