Skip to main content
Log in

Expression and function analysis of a rice OsHSP40 gene under salt stress

  • Research Article
  • Published:
Genes & Genomics Aims and scope Submit manuscript

Abstract

Heat shock proteins (HSPs) play essential roles in both plant growth and abiotic stress tolerance. In rice, OsHSP40 was recently reported to regulate programmed cell death (PCD) of suspension cells under high temperature. However, the expression and functions of OsHSP40 under normal growth or other abiotic stress conditions is still unknown. We reported the expression and function of a rice OsHSP40 gene under salt stress. Homologous proteins of OsHSP40 were collected from the NCBI database and constructed the neighbor-joining (NJ) phylogenetic tree. The expression pattern of OsHSP40 was detected by qRT-PCR under NaCl (150 mM) treatment. Then, identified a rice T-DNA insertion mutant oshsp40. At last, we compared and analyzed the phenotypes of oshsp40 and wild type under salt stress. OsHSP40 was a constitutively expressed small HSP (sHSP) gene and was close related to other plant sHSPs. Moreover, the expression of OsHSP40 was regulated by salt, varying across time points and tissues. Furthermore, the growth of T-DNA insertion mutant of OsHSP40 (designated as oshsp40) was suppressed by NaCl (150 mM) compared with that of the WT at seedling stage. Detailed measurement showed root and shoot length of the oshsp40 seedlings were significantly shorter than those of the WT seedlings under NaCl stress. In addition, the pot experiment results revealed that seedlings of oshsp40 withered more seriously compared with those of WT after NaCl treatment and recovery, and that survival rate and fresh weight of oshsp40 seedlings were significantly reduced. Taken together, these data suggested that OsHSP40 had multiple functions in rice normal growth and abiotic stress tolerance.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Asif MH, Lakhwani D, Pathak S, Bhambhani S, Bag SK, Trivedi PK (2014) Genome-wide identification and expression analysis of the mitogen-activated protein kinase gene family from banana suggest involvement of specific members in different stages of fruit ripening. Funct Integr Genom 14:161–175

    Article  CAS  Google Scholar 

  • Bernfur K, Rutsdottir G, Emanuelsson C (2017) The chloroplast-localized small heat shock protein Hsp21 associates with the thylakoid membranes in heat-stressed plants. Protein Sci 26(9):1773–1784

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cui J, Chen B, Wang HJ, Han Y, Chen X, Zhang W (2016) Glucosidase II β-subunit, a novel substrate for caspase-3-like activity in rice, plays as a molecular switch between autophagy and programmed cell death. Sci Rep 6:31764

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hsu JL, Wang LY, Wang SY, Lin CH, Ho KC, Shi FK, Chang IF (2009) Functional phosphoproteomic profiling of phosphorylation sites in membrane fractions of salt-stressed Arabidopsis thaliana. Proteome Sci 7:42

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jacob P, Hirt H, Bendahmane A (2017) The heat-shock protein/chaperone network and multiple stress resistance. Plant Biotechnol J 15(4):405–414

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Joly AL, Wettstein G, Mignot G, Ghiringhelli F, Garrido C (2010) Dual role of heat shock proteins as regulators of apoptosis and innate immunity. J Innate Immun 2:238–247

    Article  CAS  PubMed  Google Scholar 

  • Khush GS (2005) What it will take to feed 5.0 billion rice consumers in 2030. Plant Mol Biol 59:1–6

    Article  CAS  PubMed  Google Scholar 

  • Lescot M, Dehais P, Thijs G, Marchal K, Moreau Y, Peer YN, Rouze´ P, Rombauts S (2002) PlantCARE, a database of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences. Nucleic Acids Res 30(1):325–327

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Li JJ, Li Y, Yin ZG, Jiang JH, Zhang MH, Guo X, Ye ZJ, Zhao Y, Xiong HY, Zhang ZY, Shao YJ, Jiang CH, Zhang HL, An G, Paek NC, Ali J, Li ZC (2017) OsASR5 enhances drought tolerance through a stomatal closure pathway associated with ABA and H2O2 signalling in rice. Plant Biotechnol J 15:183–196

    Article  CAS  PubMed  Google Scholar 

  • Liao PF, Huang JQ, Tong PG, Nie W, Yan X, Feng YM, Peng H, Peng XJ, Li SB (2017) Characterization and expression analysis of inositolphosphorylceramide synthase family genes in rice (Oryza sativa L.). Genes Genomics 39:485–492

    Article  CAS  Google Scholar 

  • Liu JL, Luo MS, Yan X, Yu C, Li SB (2016) Characterization of genes coding for galacturonosyltransferaselike (GATL) proteins in rice. Genes Genomics 38:917–929

    Article  CAS  Google Scholar 

  • Mcloughlin F, Basha E, Fowler ME, Kim M, Bordowitz J, Katiyar-Aqarwal S, Vierling E (2016) Class I and II small heat shock proteins together with HSP101 protect protein translation factors during heat stress. Plant Physiol 172(2):1221–1236

    CAS  PubMed  PubMed Central  Google Scholar 

  • Murakami T, Matsuba S, Funatsuki H, Kawaguchi K, Saruyama H, Tanida M, Sato Y (2004) Over-expression of a small heat shock protein, sHSP17.7, confers both heat tolerance and UV-B resistance to rice plants. Mol Breed 13:165–175

    Article  CAS  Google Scholar 

  • Ruibal C, Castro A, Carballo V, Szabados L, Vidal S (2013) Recovery from heat, salt and osmotic stress in Physcomitrella patens requires a functional small heat shock protein PpHsp16.4. BMC Plant Biol 13:174–191

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:406–425

    CAS  PubMed  Google Scholar 

  • Sarkar NK, Kim YK, Grover A (2009) Rice sHsp genes: genomic organization and expression profiling under stress and development. BMC Genomics 10:393

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Shen C, Que Z, Xia Y, Tang N, Li D, He R, Cao M (2017) Knock out of the annexin gene OsAnn3, via crispr/cas9-mediated genome editing decreased cold tolerance in rice. J Plant Biol 60:539–547

    Article  CAS  Google Scholar 

  • Sun W, Bernard C, Van De Cotte B, Van Montagu M, Verbruggen N (2001) At-HSP17.6A, encoding a small heat-shock protein in Arabidopsis, can enhance osmotolerance upon overexpression. Plant J 27:407–415

    Article  CAS  PubMed  Google Scholar 

  • Sun W, Montagu MV, Verbruggen N (2002) Small heat shock proteins and stress tolerance in plants. Biochim Biophys Acta 1577:1–9

    Article  CAS  PubMed  Google Scholar 

  • Tester M, Langridge P (2010) Breeding technologies to increase crop production in a changing world. Science 327:818–822

    Article  CAS  PubMed  Google Scholar 

  • Tian L, Wang XY, Wang XP, Lei CL, Zhu F (2018) Starvation-, thermal- and heavy metal-associated expression of four small heat shock protein genes in musca domestica. Gene 642:268–276

    Article  CAS  PubMed  Google Scholar 

  • Trent J (1996) A review of acquired thermotolerance, heat-shock proteins, and molecular chaperones in archaea. FEMS Microbiol Rev 18:249–258

    Article  CAS  Google Scholar 

  • Venkatesh J, Park SW (2015) Genome-wide analysis and expression profiling of DNA-binding with one zinc finger (Dof) transcription factor family in potato. Plant Physiol Biochem 94:73–85

    Article  CAS  PubMed  Google Scholar 

  • Vermeulen S, Zougmore R, Wollenberg E, Thornton P, Nelson G, Kristjanson P, Kinyangi J, Jarvis A, Hansen J, Challinor A, Acmpbell B, Aggarwal P (2012) Climate change, agriculture and food security: a global partnership to link research and action for low-income agricultural producers and consumers. Curr Opin Environ Sustain 4:128–133

    Article  Google Scholar 

  • Vierling E (1991) The roles of heat shock proteins in plants. Annu Rev Plant Biol 42:579–620

    Article  CAS  Google Scholar 

  • Wang YS, An CY, Zhang XD, Yao JQ, Zhang YP, Sun YJ, Yu FH, Amador DM, Mou ZL (2013) The Arabidopsis elongator complex subunit2 epigenetically regulates plant immune responses. Plant Cell 25:762–776

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Wang X, Zhou W, Lu ZH, Ouyang YD, O CS, Yao JL (2015a) A lipid transfer protein, OsLTPL36, is essential for seed development and seed quality in rice. Plant Sci 239:200–208

    Article  CAS  PubMed  Google Scholar 

  • Wang AQ, Yu XH, Mao Y, Liu Y, Liu GQ, Liu YS, Niu XL (2015b) Overexpression of a small heat-shock-protein gene enhances tolerance to abiotic stresses in rice. Plant Breed 134(4):384–393

    Article  CAS  Google Scholar 

  • Wang D, Qu ZP, Yang L, Zhang QZ, Liu ZH, Do T, Adelson DL, Wang ZY, Searle I, Zhu JK (2017) Transposable elements (TEs) contribute to stress-related long intergenic noncoding RNAs in plants. Plant J 90:133–146

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Xue LJ, Zhang JJ, Xue HW (2009) Characterization and expression profiles of miRNAs in rice seeds. Nucleic Acids Res 37(3):916–930

    Article  CAS  PubMed  Google Scholar 

  • Ye SF, Yu SW, Shu LB, Wu JH, Wu AZ, Luo LJ (2012) Expression profile analysis of 9 heat shock protein genes throughout the life cycle and under abiotic stress in rice. Chin Sci Bull 57(4):336–343

    Article  CAS  Google Scholar 

  • Yi J, An G (2013) Utilization of T-DNA tagging lines in rice. J Plant Biol 56(2):85–90

    Article  CAS  Google Scholar 

  • Zhai M, Sun Y, Jia C, Peng S, Liu Z, Yang G (2016) Over-expression of JrsHSP17.3 gene from Juglans regia confer the tolerance to abnormal temperature and NaCl stresses. J Plant Biol 59:549–558

    Article  CAS  Google Scholar 

  • Zhang Q (2007) Strategies for developing Green Super Rice. Proc Natl Acad Sci USA 104:16402–16409

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

This research was supported by grants from the National Natural Science Foundation of China (Nos. 31760080, 31460279, 31560383 and 31660296).

Author information

Authors and Affiliations

Authors

Contributions

XW, JO and SL designed research; HZ and LS performed research; HP and XY did bioinformatic analysis and revised the manuscript; XW, JO and SL wrote the paper. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Jie-Xiu Ouyang or Shao-Bo Li.

Ethics declarations

Conflict of interest

The authors declare that they have no competing interests.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Fig. S1 Expression profile of

OsHSP40in different tissues of ZH11 based on microarray analysis. The scores are the average expression values obtained from microarrays. (TIF 223 KB)

Supplementary material 2 (DOCX 18 KB)

Supplementary material 3 (DOCX 11 KB)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wang, X., Zhang, H., Shao, LY. et al. Expression and function analysis of a rice OsHSP40 gene under salt stress. Genes Genom 41, 175–182 (2019). https://doi.org/10.1007/s13258-018-0749-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13258-018-0749-2

Keywords

Navigation