Exploring salt tolerance mechanisms using machine learning for transcriptomic insights: case study in Spartina alterniflora

Zhangping Huang , Shoukun Chen , Kunhui He , Tingxi Yu , Junjie Fu , Shang Gao , Huihui Li

Horticulture Research ›› 2024, Vol. 11 ›› Issue (5) : 082

PDF (2393KB)
Horticulture Research ›› 2024, Vol. 11 ›› Issue (5) :082 DOI: 10.1093/hr/uhae082
Articles
research-article
Exploring salt tolerance mechanisms using machine learning for transcriptomic insights: case study in Spartina alterniflora
Author information +
History +
PDF (2393KB)

Abstract

Salt stress poses a significant threat to global cereal crop production, emphasizing the need for a comprehensive understanding of salt tolerance mechanisms. Accurate functional annotations of differentially expressed genes are crucial for gaining insights into the salt tolerance mechanism. The challenge of predicting gene functions in under-studied species, especially when excluding infrequent GO terms, persists. Therefore, we proposed the use of NetGO 3.0, a machine learning-based annotation method that does not rely on homology information between species, to predict the functions of differentially expressed genes under salt stress. Spartina alterniflora, a halophyte with salt glands, exhibits remarkable salt tolerance, making it an excellent candidate for in-depth transcriptomic analysis. However, current research on the S. alterniflora transcriptome under salt stress is limited. In this study we used S. alterniflora as an example to investigate its transcriptional responses to various salt concentrations, with a focus on understanding its salt tolerance mechanisms. Transcriptomic analysis revealed substantial changes impacting key pathways, such as gene transcription, ion transport, and ROS metabolism. Notably, we identified a member of the SWEET gene family in S. alterniflora, SA_12G129900.m1, showing convergent selection with the rice ortholog SWEET15. Additionally, our genome-wide analyses explored alternative splicing responses to salt stress, providing insights into the parallel functions of alternative splicing and transcriptional regulation in enhancing salt tolerance in S. alterniflora. Surprisingly, there was minimal overlap between differentially expressed and differentially spliced genes following salt exposure. This innovative approach, combining transcriptomic analysis with machine learning-based annotation, avoids the reliance on homology information and facilitates the discovery of unknown gene functions, and is applicable across all sequenced species.

Cite this article

Download citation ▾
Zhangping Huang, Shoukun Chen, Kunhui He, Tingxi Yu, Junjie Fu, Shang Gao, Huihui Li. Exploring salt tolerance mechanisms using machine learning for transcriptomic insights: case study in Spartina alterniflora. Horticulture Research, 2024, 11 (5) : 082 DOI:10.1093/hr/uhae082

登录浏览全文

4963

注册一个新账户 忘记密码

Acknowledgements

This work was financially supported by National Key R&D Program of China (2023ZD04073), the Nanfan special project, CAAS, Grant No. YBXM2304, and the Innovation Program of the Chinese Academy of Agricultural Sciences.

Author contributions

H.H.L. conceived the original idea, designed the experiments, and provided overall supervision and direction of the work. Z.P.H., S.K.C., K.H.H., and T.X.Y. performed the experiments and data analysis. J.J.F. and S.G. provided valuable advice for the experimental design and optimization. Z.P.H., S.K.C., and H.H.L. wrote the manuscript. All authors discussed and commented on the manuscript.

Data availability

All relevant data can be found within the paper and its supporting materials.

Conflict of interest

The authors declare no conflicts of interest.

Supplementary data

Supplementary data are available at Horticulture Research online.

References

[1]

Yang J, Yan R, Roy A. et al. The I-TASSER suite: protein structure and function prediction. Nat Methods. 2015; 12:7-8

[2]

Lachmann A, Rizzo KA, Bartal A. et al. PrismEXP: gene annotation prediction from stratified gene-gene co-expression matrices. PeerJ. 2023; 11:e14927.

[3]

Zhou N, Jiang Y, Bergquist TR. et al. The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens. Genome Biol. 2019; 20:244

[4]

Lee J, Yoon W, Kim S. et al. BioBERT: a pre-trained biomedical language representation model for biomedical text mining. Bioinformatics. 2020; 36:1234-40

[5]

Rives A, Meier J, Sercu T. et al. Biological structure and function emerge from scaling unsupervised learning to 250 million protein sequences. Proc Natl Acad Sci USA. 2021; 118:2016239118.

[6]

Alley EC, Khimulya G, Biswas S. et al. Unified rational protein engineering with sequence-based deep representation learning. Nat Methods. 2019; 16:1315-22

[7]

Wang S, You R, Liu Y. et al. NetGO 3.0: a protein language model improves large-scale functional annotations. Genom Proteom Bioinf. 2023; 21:349-58

[8]

Mishra A, Tanna B. Halophytes: potential resources for salt stress tolerance genes and promoters. Front Plant Sci. 2017; 8:829

[9]

Jarvis DE, Ho YS, Lightfoot DJ. et al. The genome of Chenopodium quinoa. Nature. 2017; 542:307-12

[10]

Yuan F, Wang X, Zhao B. et al. The genome of the recretohalophyte Limonium bicolor provides insights into salt gland development and salinity adaptation during terrestrial evolution. Mol Plant. 2022; 15:1024-44

[11]

Flowers TJ, Colmer TD. Plant salt tolerance: adaptations in halophytes. Ann Bot. 2015; 115:327-31

[12]

Sengupta S, Pehlivan N, Mangu V. et al. Characterization of a stress-enhanced promoter from the grass halophyte, Spartina alterniflora L. Biology. 2022; 11:1828.

[13]

Biradar H, Karan R, Subudhi PK.Transgene pyramiding of salt responsive protein3-1 ( SaSRP3-1) and SaVHAc1 from Spartina alterniflora L. enhances salt tolerance in rice. Front Plant Sci. 2018; 9:1304.

[14]

Yin H, Li M, Li D. et al. Transcriptome analysis reveals regulatory framework for salt and osmotic tolerance in a succulent xerophyte. BMC Plant Biol. 2019; 19:88

[15]

Zhou Y, Yang P, Cui F. et al. Transcriptome analysis of salt stress responsiveness in the seedlings of Dongxiang wild rice (Oryza rufipogon Griff.). PLoS One. 2016; 11:e0146242.

[16]

Zhang X, Liu J, Huang Y. et al. Comparative transcriptomics reveals the molecular mechanism of the parental lines of maize hybrid An’nong876 in response to salt stress. Int J Mol Sci. 2022; 23:5231.

[17]

Cha JY, Kang SH, Ji MG. et al. Transcriptome changes reveal the molecular mechanisms of humic acid-induced salt stress tolerance in Arabidopsis. Molecules. 2021; 26:782.

[18]

Han F, Sun M, He W. et al. Transcriptome analysis reveals molecular mechanisms under salt stress in leaves of foxtail millet (Setaria italica L.). Plants (Basel). 2022; 11:1864.

[19]

Wang L, Du M, Wang B. et al. Transcriptome analysis of halophyte Nitraria tangutorum reveals multiple mechanisms to enhance salt resistance. Sci Rep. 2022; 12:14031

[20]

Kulmanov M, Hoehndorf R. DeepGOPlus: improved protein function prediction from sequence. Bioinformatics. 2020; 36:422-9

[21]

Yang M, Chen S, Huang Z. et al. Deep learning-enabled discovery and characterization of HKT genes in Spartina alterniflora. Plant J. 2023; 116:690-705

[22]

Ye W, Wang T, Wei W. et al. The full-length transcriptome of Spartina alterniflora reveals the complexity of high salt tolerance in monocotyledonous halophyte. Plant Cell Physiol. 2020; 61:882-96

[23]

You R, Yao S, Xiong Y. et al. NetGO: improving large-scale protein function prediction with massive network information. Nucleic Acids Res. 2019; 47:W379-87

[24]

Yao S, You R, Wang S. et al. NetGO 2.0: improving large-scale protein function prediction with massive sequence, text, domain, family and network information. Nucleic Acids Res. 2021; 49:W469-75

[25]

Imran S, Tsuchiya Y, Tran STH. et al. Identification and characterization of rice OsHKT1;3 variants. Plants (Basel). 2021; 10:2006

[26]

Shahzad B, Shabala L, Zhou M. et al. Comparing essentiality of SOS1-mediated Na+ exclusion in salinity tolerance between cultivated and wild rice species. Int J Mol Sci. 2022; 23:9900

[27]

Aziz S, Germano TA, KLL T. et al. Transcriptome analyses in a selected gene set indicate alternative oxidase (AOX) and early enhanced fermentation as critical for salinity tolerance in rice. Plants (Basel). 2022; 11:2145

[28]

Mathan J, Singh A, Ranjan A. Sucrose transport in response to drought and salt stress involves ABA-mediated induction of OsSWEET13 and OsSWEET 15 in rice. Physiol Plant. 2021; 171:620-37

[29]

Reddy AS, Marquez Y, Kalyna M. et al. Complexity of the alternative splicing landscape in plants. Plant Cell. 2013; 25:3657-83

[30]

Zhang P, Deng H, Xiao F. et al. Alterations of alternative splicing patterns of Ser/Arg-rich (SR) genes in response to hormones and stresses treatments in different ecotypes of rice (Oryza sativa). J Integr Agric. 2013; 12:737-48

[31]

Guo W, Yu K, Han L. et al. Global profiling of alternative splicing landscape responsive to salt stress in wheat (Triticum aestivum L.). Plant Growth Regul. 2020; 92:107-16

[32]

Huang Z, Ye J, Zhai R. et al. Comparative transcriptome analysis of the heterosis of salt tolerance in inter-subspecific hybrid rice. Int J Mol Sci. 2023; 24:2212.

[33]

Wang M, Wang Y, Zhang Y. et al. Comparative transcriptome analysis of salt-sensitive and salt-tolerant maize reveals potential mechanisms to enhance salt resistance. Genes Genomics. 2019; 41:781-801

[34]

Abid M, Gu S, Zhang YJ. et al. Comparative transcriptome and metabolome analysis reveal key regulatory defense networks and genes involved in enhanced salt tolerance of Actinidia (kiwifruit). Hortic Res. 2022; 9:uhac189

[35]

Cheng Y, Sun J, Jiang M. et al. Chromosome-scale genome sequence of Suaeda glauca sheds light on salt stress tolerance in halophytes. Hortic Res. 2023; 10:uhad161

[36]

Zhang D, He S, Fu Y. et al. Transcriptome analysis reveals key genes in response to salinity stress during seed germination in Setaria italica. Environ Exp Bot. 2021; 191:104604.

[37]

Vaziriyeganeh M, Khan S, Zwiazek JJ. Transcriptome and metabolome analyses reveal potential salt tolerance mechanisms contributing to maintenance of water balance by the halophytic grass Puccinellia nuttalliana. Front Plant Sci. 2021; 12:760863.

[38]

Yu H, Du Q, Campbell M. et al. Genome-wide discovery of natural variation in pre-mRNA splicing and prioritising causal alternative splicing to salt stress response in rice. New Phytol. 2021; 230:1273-87

[39]

Zhang X, Liu P, Qing C. et al. Comparative transcriptome analyses of maize seedling root responses to salt stress. PeerJ. 2021; 9:e10765.

[40]

Seifikalhor M, Aliniaeifard S, Shomali A. et al. Calcium signaling and salt tolerance are diversely entwined in plants. Plant Signal Behav. 2019; 14:1665455

[41]

Hong Y, Guan X, Wang X. et al. Natural variation in SlSOS2 promoter hinders salt resistance during tomato domestication. Hortic Res. 2023; 10:uhac244

[42]

Chaves-Sanjuan A, Sanchez-Barrena MJ, Gonzalez-Rubio JM. et al. Structural basis of the regulatory mechanism of the plant CIPK family of protein kinases controlling ion homeostasis and abiotic stress. Proc Natl Acad Sci USA. 2014; 111:E4532-41

[43]

Zhou X, Li J, Wang Y. et al. The classical SOS pathway confers natural variation of salt tolerance in maize. New Phytol. 2022; 236:479-94

[44]

Jin Y, Jing W, Zhang Q. et al. Cyclic nucleotide gated channel 10 negatively regulates salt tolerance by mediating Na+ transport in Arabidopsis. J Plant Res. 2015; 128:211-20

[45]

Kugler A, Köhler B, Palme K. et al. Salt-dependent regulation of a CNG channel subfamily in Arabidopsis. BMC Plant Biol. 2009; 9:140

[46]

Yadav AK, Shankar A, Jha SK. et al. A rice tonoplastic calcium exchanger, OsCCX2 mediates Ca2+/cation transport in yeast. Sci Rep. 2015; 5:17117

[47]

Singh A, Kanwar P, Yadav AK. et al. Genome-wide expressional and functional analysis of calcium transport elements during abiotic stress and development in rice. FEBS J. 2014; 281:894-915

[48]

Yang J, Luo D, Yang B. et al. SWEET11 and 15 as key players in seed filling in rice. New Phytol. 2018; 218:604-15

[49]

Chen LQ, Lin IW, Qu XQ. et al. A cascade of sequentially expressed sucrose transporters in the seed coat and endosperm provides nutrition for the Arabidopsis embryo. Plant Cell. 2015; 27:607-19

[50]

Wu Y, Wang S, Du W. et al. Sugar transporter ZmSWEET1b is responsible for assimilate allocation and salt stress response in maize. Funct Integr Genomics. 2023; 23:137

[51]

Li J, Gao X, Chen X. et al. Comparative transcriptome responses of leaf and root tissues to salt stress in wheat strains with different salinity tolerances. Front Genet. 2023; 14:1015599

[52]

Liu Z, Qin J, Tian X. et al. Global profiling of alternative splicing landscape responsive to drought, heat and their combination in wheat (Triticum aestivum L.). Plant Biotechnol J. 2018; 16:714-26

[53]

Zhu G, Li W, Zhang F. et al. RNA-seq analysis reveals alternative splicing under salt stress in cotton, Gossypium davidsonii. BMC Genomics. 2018; 19:73

[54]

Ding F, Cui P, Wang Z. et al. Genome-wide analysis of alternative splicing of pre-mRNA under salt stress in Arabidopsis. BMC Genomics. 2014; 15:431

[55]

Li W, Lin WD, Ray P. et al. Genome-wide detection of condition-sensitive alternative splicing in Arabidopsis roots. Plant Physiol. 2013; 162:1750-63

[56]

Ling Z, Zhou W, Baldwin IT. et al. Insect herbivory elicits genome-wide alternative splicing responses in Nicotiana attenuata. Plant J. 2015; 84:228-43

[57]

Kim D, Pertea G, Trapnell C. et al. TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biol. 2013; 14:R36

[58]

Ernst J, Bar-Joseph Z. STEM: a tool for the analysis of short time series gene expression data. BMC Bioinformatics. 2006; 7:191

[59]

Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-ΔΔCT) method. Methods. 2001; 25:402-8

[60]

Magis C, Taly JF, Bussotti G. et al. T-Coffee: tree-based consistency objective function for alignment evaluation. Methods Mol Biol. 2014; 1079:117-29

[61]

Kumar S, Stecher G, Tamura K. MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Mol Biol Evol. 2016; 33:1870-4

[62]

Castoe TA, de Koning APJ, Kim HM. et al. Evidence for an ancient adaptive episode of convergent molecular evolution. Proc Natl Acad Sci USA. 2009; 106:8986-91

[63]

Shen S, Park JW, Lu ZX. et al. rMATS: robust and flexible detection of differential alternative splicing from replicate RNA-Seq data. Proc Natl Acad Sci USA. 2014; 111:E5593-601

PDF (2393KB)

121

Accesses

0

Citation

Detail

Sections
Recommended

/