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A glycine-rich RNA-binding protein can mediate physiological responses in transgenic plants under salt stress

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Abstract

Glycine-rich RNA-binding proteins (GRPs) are involved in post-transcriptional regulation of genes, which have been found to play a role in stress response. However, whether GRPs can mediate some physiological responses related to salt stress tolerance is still not known. In the present study, we investigated the role of GRPs in salt stress-induced physiological responses by generating transgenic tobacco lines overexpressing a GRP (LbGRP1) gene from Limonium bicolor (Bunge) Kuntze. Compared with wild type (WT) tobacco, the transgenic plants showed significantly improved superoxide dismutase and catalase activities under salt stress conditions. Levels of proline in the transgenic plants were significantly higher than those in the WT plants grown under NaCl stress conditions. Furthermore, Na+ content and Na+/K+ ratio in the transgenic plants were lower than those in the WT plants under both normal growth and stress conditions. These results suggested that overexpression of the LbGRP1 gene can affect some physiological processes associated with salt tolerance of plants. Therefore, we hypothesize that LbGST1 can enhance stress resistance by mediating some physiological pathways.

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References

  1. Lee MO, Kim KP, Kim BG, Hahn JS, Hong CB (2009) Flooding stress-induced glycine-rich RNA-binding protein from Nicotiana tabacum. Mol Cells 27(1):47–54

    Article  PubMed  CAS  Google Scholar 

  2. Kim YO, Pan S, Jung CH, Kang H (2007) A zinc finger-containing glycine-rich RNA-binding protein, atRZ-1a, has a negative impact on seed germination and seedling growth of Arabidopsis thaliana under salt or drought stress conditions. Plant Cell Physiol 48(8):1170–1181

    Article  PubMed  CAS  Google Scholar 

  3. Palusa SG, Ali GS, Reddy AS (2007) Alternative splicing of pre-mRNAs of Arabidopsis serine/arginine-rich proteins: regulation by hormones and stresses. Plant J 49:1091–1107

    Article  PubMed  CAS  Google Scholar 

  4. Carpenter CD, Kreps JA, Simon AE (1994) Genes encoding glycine-rich Arabidopsis thaliana proteins with RNA-binding motifs are influenced by cold treatment and an endogenous circadian rhythm. Plant Physiol 104(3):1015–1025

    Article  PubMed  CAS  Google Scholar 

  5. Kwak KJ, Kim YO, Kang H (2005) Characterization of transgenic Arabidopsis plants overexpressing GR-RBP4 under high salinity, dehydration, or cold stress. J Exp Bot 56(421):3007–3016

    Article  PubMed  CAS  Google Scholar 

  6. Kim JY, Kim WY, Kwak KJ, Oh SH, Han YS, Kang H (2010) Zinc finger-containing glycine-rich RNA-binding protein in Oryza sativa has an RNA chaperone activity under cold stress conditions. Plant Cell Environ 33:759–768

    Article  PubMed  CAS  Google Scholar 

  7. Kim JY, Kim WY, Kwak KJ, Oh SH, Han YS, Kang H (2010) Glycine-rich RNA-binding proteins are functionally conserved in Arabidopsis thaliana and Oryza sativa during cold adaptation process. J Exp Bot 61(9):2317–2325

    Article  PubMed  CAS  Google Scholar 

  8. Kim JS, Park SJ, Kwak KJ, Kim YO, Kim JY, Song J, Jang B, Jung CH, Kang H (2007) Cold shock domain proteins and glycine-rich RNA-binding proteins from Arabidopsis thaliana can promote the cold adaptation process in Escherichia coli. Nucleic Acids Res 35(2):506–516

    Article  PubMed  CAS  Google Scholar 

  9. Kim JS, Jung HJ, Lee HJ, Kim KA, Goh CH, Woo Y, Oh SH, Han YS, Kang H (2008) Glycine-rich RNA-binding protein 7 affects abiotic stress responses by regulating stomata opening and closing in Arabidopsis thaliana. Plant J 55(3):455–466

    Article  PubMed  CAS  Google Scholar 

  10. Wang YC, Ma H, Liu GF, Zhang DW, Ban QY, Zhang GD, Xu CX, Yang CP (2008) Generation and analysis of expressed sequence tags from a NaHCO3-treated Limonium bicolor cDNA library. Plant Physiol Biochem 46(11):977–986

    Article  PubMed  CAS  Google Scholar 

  11. Elstner EF, Heupel A (1976) Inhibition of nitrite formation from hydroxylammonium chloride-simple assay for superoxide dismutase. Anal Biochem 70:616–620

    Article  PubMed  CAS  Google Scholar 

  12. Beers RF, Sizer IW (1952) Spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem 195:133–140

    PubMed  CAS  Google Scholar 

  13. Bates LE, Waldren RP, Teare ID (1973) Rapid determination of free proline for water stress studies. Plant Soil 39:205–207

    Article  CAS  Google Scholar 

  14. Touyz RM, Milne FJ (1991) A method for determining the total magnesium, calcium, sodium and potassium contents of human platelets. Miner Electrolyte Metab 17:173–178

    PubMed  CAS  Google Scholar 

  15. Agarwal P, Agarwal PK, Joshi AJ, Sopory SK, Reddy MK (2010) Overexpression of PgDREB2A transcription factor enhances abiotic stress tolerance and activates downstream stress-responsive genes. Mol Biol Rep 37:1125–1135

    Article  PubMed  CAS  Google Scholar 

  16. Wu S, Su Q, An LJ (2010) Isolation of choline monooxygenase (CMO) gene from Salicornia europaea and enhanced salt tolerance of transgenic tobacco with CMO genes. Indian J Biochem Biophys 47:298–305

    PubMed  CAS  Google Scholar 

  17. Leshem Y, Seri L, Levine A (2007) Induction of phosphatidylinositol 3-kinase-mediated endocytosis by salt stress leads to intracellular production of reactive oxygen species and salt tolerance. Plant J 51:185–197

    Article  PubMed  CAS  Google Scholar 

  18. Xu DQ, Huang J, Guo SQ, Yang X, Bao YM, Tang HJ (2008) Overexpression of a TFIIIAtype zinc finger protein gene ZFP252 enhances drought and salt tolerance in rice (Oryza sativa L.). FEBS Lett 582:1037–1043

    Article  PubMed  CAS  Google Scholar 

  19. Trovato M, Mattioli R, Costantino P (2008) Multiple roles of proline in plant stress tolerance and development. Rendiconti Lincei 19:325–346

    Article  Google Scholar 

  20. Mansour M (1998) Protection of plasma membrane of onion epidermal cells by glycinebetaine and proline against NaCl stress. Plant Physiol Biochem 36:767–772

    Article  CAS  Google Scholar 

  21. Srinivas V, Balasubramanian D (1995) Proline is a protein-compatible hydrotrope. Langmuir 11:2830–2833

    Article  CAS  Google Scholar 

  22. Tester M, Davenport R (2003) Na+ tolerance and Na+ transport in higher plants. Ann Bot 91:503–527

    Article  PubMed  CAS  Google Scholar 

  23. Garg A, Kim JK, Owens TG, Raneala AP, Chio YD, Kochian LV, Wu R (2002) Trehalose accumulation in rice plants confers high tolerance levels to different abiotic stresses. Proc Natl Acad Sci USA 99:15898–15903

    Article  PubMed  CAS  Google Scholar 

  24. Obata T, Kitamoto HK, Nakamura A, Fukuda A, Tanaka Y (2007) Rice shaker potassium channel OsKAT1 confers tolerance to salinity stress on yeast and rice cells. Plant Physiol 144:1978–1985

    Article  PubMed  CAS  Google Scholar 

  25. Kishor P, Hong Z, Miao GH, Hu C, Verma D (1995) Overexpression of [delta]-pyrroline-5-carboxylate synthetase increases proline production and confers osmo tolerance in transgenic plants. Plant Physiol 108:1387–1394

    PubMed  CAS  Google Scholar 

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Acknowledgments

This work was supported by Fundamental Research Funds for the Central Universities (DL09DA01), Genetically modified organisms breeding major projects (2009ZX08009-098B) and National High Technology Research and Development Program of China (863 Program) (2009AA10Z107).

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Correspondence to Chuan-Ping Yang.

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Wang, C., Zhang, DW., Wang, YC. et al. A glycine-rich RNA-binding protein can mediate physiological responses in transgenic plants under salt stress. Mol Biol Rep 39, 1047–1053 (2012). https://doi.org/10.1007/s11033-011-0830-2

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  • DOI: https://doi.org/10.1007/s11033-011-0830-2

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