DIFFERENTIAL GENE EXPRESSION IN RESPONSE TO SALT STRESS IN Vicia monantha

Authors

  • REEM M. ABD EL-MAKSOUD Agricultural Genetic Engineering Research Institute (AGERI), Agricultural Research Center (ARC), Giza, Egypt
  • A. M. AGEEZ1 Agricultural Genetic Engineering Research Institute (AGERI), Agricultural Research Center (ARC), Giza, Egyp
  • DINA A. EL-KHISHIN Agricultural Genetic Engineering Research Institute (AGERI), Agricultural Research Center (ARC), Giza, Egypt
  • EMAN M. FAHMY
  • FATTHY M. ABDEL-TAWAB Department of Genetics, Faculty of Agriculture, Ain Shams University, Cairo

Abstract

Vicia monantha is a member of the family Fabaceae, belonging to the genus Vicia. It is a wild plant species that is native to the Northern African region, particularly Algeria and Egypt. It is char- acterized by its noticeable withstanding of severe environmental conditions. Such wild plants are considered as an excellent source of stress-related genes awaiting their isolation and identification.
Some species of Vicia, such as V. faba (broad bean), V. narbonensis (narbon vetch), V. villosa (hairy vetch) and V. sativa (common vetch), represent eco- nomically important crops that are widely cultivated as a green manure cover, as well as grain and straw crops for animals and a soil binder throughout the North Temperate Zone of the new and old worlds.
Wild Vicia species, such as V. cordata, V. nigra, V. narbonensis, V. sativa, V. monantha and V. villosa, are of great interest to agronomists and plant breeders as crop plants in their own right and as possible sources of germplasm for cultivated Vicia faba (Atlas of legume plant of the North West of Egypt, 1993).
Plants are frequently exposed to stresses, which are usually defined as external factors exerting disadvantageous influences on them (Levitt, 1972). Water deficit, chilling and freezing, heat stress, salinity and oxygen deficiency are major stress factors restricting plant growth (Boyer, 1982; Salisbury and Ross, 1989). Some of which (such as temperature) can become stressful in a few minutes; others may take days to weeks (soil water) or even months (mineral nutrients) to become stressful. Salinity can affect any process in the plant life cycle, so that tolerance will involve a complex interplay of characters. Many researchers investi- gated details of the physiology and biochemistry of salt tolerance and also looked at methods to screen overall plant performance that could be used in breeding programs. In general, plants are relatively tolerant during germination but become more sensitive during emergence and early seedling up to later stages of growth (Azhar and McNeilly, 1989; Abdel-Tawab et al., 1998). Drought and salinity are becoming particularly wide- spread in many regions, and are expected to cause serious salinization of more than 50% of all arable lands by the year 2050. Drought, salinity, extreme temperatures and oxidative stress are often intercon- nected, and may induce similar cellular damage. For example, drought and/or salinization are manifested primarily as osmotic stress, resulting in the disruption of homeostasis and ion distribution in the cell (Serrano et al. 1999; Zhu, 2001).
Cloning and characterization of environmental stress-induced genes have greatly contributed to our understanding of the physiological responses of plant cells at the molecular level to different environmental factors. cDNA-amplified fragment length polymorphism (cDNA- AFLP) is an efficient, sensitive, and re- producible technology for the isolation of differentially expressed genes (Bachem et al., 1996). It requires no prior sequence information and is, therefore, a useful tool for the identification of novel genes (Ditt et al., 2001). cDNA-AFLP is widely avail- able at a low cost for various plant spe- cies, even if there is little information at the molecular level (Breyne and Zabeau, 2001; Bei et al., 2006; El-Khishin, 2003; Ge et al., 2007; Niranjan et al., 2006; Roshandel, 2007). It is a polymerase chain reaction (PCR)-based technology like differential display (DD), but featuring higher reproducibility and availability. The most critical advantage is that cDNA- AFLP is based on linker-ligated PCR, whereas DD is based on arbitrarily primed PCR (Bachem et al., 1996; Pardee and McClelland, 1999; Shokry et al., 2007).
The objective of this study was to isolate and characterize some of the key expressed sequence tags (ESTs) in re- sponse to salt stress in Vicia monantha using cDNA-AFLP technique, clone and sequence the isolated ESTs and determine gene functions for each EST.

Author Biography

  • EMAN M. FAHMY

    Genetics Dept., Fac. Agric., Ain Shams Univ., Shoubra El-Kheima, Cairo, Egypt

References

Abdel-Tawab, F. M., R. S. Dhindsa, M. A. Rashed, A. Bahieldin and A. Abo- Doma (1998). Molecular genetic markers for salt tolerance in sorghum. International Congress on Molecular Genetics, Cairo, Egypt (21- 25 Feb), 1: 195-204.

Aly, A. E. and M. T. Hassan (1993). Atlas of legume plants of the North West coastal of Egypt.

Azhar, F. M. and T. McNeilly (1989). The response of four sorghum acces- sions/cultivars to salinity during plant development. J. Agronomy and Crop Science, 163: 33-43.

Bachem, C. W., R. S. van der Hoeven, S. M. de Bruijn, D. Vreugdenhil, C. W. B. Bachem, R. S. van der Hoeve., S. M. de Bruijn, D. Vreugdenhil, M. Zabeau and R. G. F. Visser (1996). Visualization of differential gene expression using a novel method of RNA fingerprint- ing based on AFLP analysis of gene expression during potato tuber development. The Plant Journal, 9: 745-753.

Bei-CaiLi, Zhang-XueYong, Wen-XiaoJie and Liu-Xu (2006). Isolation of TaVHA-C, a gene in wheat related to salt-tolerance via cDNA-AFLP. Scientia-Agricultura-Sinica, 39: 1736-1742.

Boyer, J. S. (1982). Plant productivity and environment science, 28: 443-448.

Breyne P. and M. Zabeau (2001). Ge- nome-wide expression analysis of plant cell cycle modulated genes. Current Opinion in Plant Biology,4: 136-142.

Ditt, R. F., E. W. Nester and L. Comai (2001). Plant gene expression response to Agrobacterium tumefa- ciens. Proceedings of the National Academy of Sciences, 98: 10954-10959.

El-Khishin, D. A. (2003). Assessment of genetic diversity in some wild and cultivated Vicia Spp. as revealed by AFLP analysis. Egypt. J. Genet. Cytol., 32: 341-356.

Ge-RongChao, Chen-GuiPing, Zhao- BaoCun, Shen-YinZhu and Huang- ZhanJing (2007). Cloning and functional characterization of a wheat serine/threonine kinase gene (TaSTK) related to salt-resistance. Plant-Science, 173: 55-60.

Hagen, G. and T. J. Guilfoyle (1985). Rapid induction of selective tran- scription by auxins. Mol. Cell Biol., 5: 1197-1203.

Hsieh, T. H., J. T. Lee, P. Z. Yang, L. H. Chiu, Y. Y. Charng, Y. C. Wang and M. T. Chan (2002a). Heterolo- gous expression of the Arabidopsis C-repeat/Dehydration Response Element Binding factor 1 gene confers elevated tolerance to chilling and oxidative stresses in transgenic tomato. Plant Physiol., 129: 1086-1094.

Hsieh, T. H., J.T. Lee, Y. Y. Charng and M. T. Chan (2002b). Tomato plants ectopically expressing Arabidopsis CBF1 show enhanced resistance to water deficit stress. Plant Physiol., 130: 618-626.

Jaglo-Ottosen, K. R., S. J. Gilmour, D. G. Zarka, O. Schabenberger and M. F. Thomashow (1998). Arabidopsis CBF1 overexpression induces COR genes and enhances freezing tolerance. Science, 280: 104-106.

Kasuga, M., Q. Liu, S. Miura, K. Yama- guchi-Shinozaki and K. Shinozaki (1999). Improving plant drought, salt, and freezing tolerance by gene transfer of a single-inducible tran- scription factor. Nature Biotech., 17: 287-291.

Kim, D. J. and S. Smith (1994). Molecular cloning of cucumber phosphoe- nolpyruvate carboxykinase and developmental regulation of gene expression. Plant Mo1. Biol., 26:423-434.

Lee, J. T., V. Prasad, P. T. Yang, J. F. Wu, TH. D. Ho, Y. Y. Chang and M. T. Chan (2003). Expression of Arabi- dopsis CBF1 regulated by an ABA/stress inducible promoter in transgenic tomato confers stress tolerance without affecting yield. Plant Cell Environ., 26: 1181-1190.

Levitt, J. (1972). Responses of plants to environmental stresses. Academic Press Inc., New York and London.

Liu, K., B. C. Kang, H. Jiang, S. L. Moore, H. Li, C. B. Watkins, T. L. Setter and M. M. Jahn (2005). A GH3-like gene, CcGH3, isolated from Capsicum chinense L. fruit is regulated by auxin and ethylene. Plant Mol. Biol., 58: 447-464.

McGrath, J. Mitchell, Abla Elawady, Dina El-Khishin, Rachel P. Naegele, Kevin M. Carr and Benildo de los Reyes (2008). Sugar beet Germina- tion: Phenotypic selection and Molecular profiling to identify genes involved in abiotic stress response. Acta Hort., 782: 35-49.

Niranjan Baisakh, Prasanta K. Subudhi and Neil P. Parami (2006). cDNA- AFLP analysis reveals differential gene expression in response to salt stress in a halophyte Spartina alterniflora Loisel. Plant Science,

: 1141-1149.

Owens, C. L., M. F. Thomashow, J. F. Hancock and A. F. Iezzoni (2002). CBF1 orthologs in sour cherry and strawberry and the heterologous expression of CBF1 in strawberry. J. Amer. Soc. Hort. Sci., 127: 489-494.

Pardee, A. B. and M. McClelland (1999). Expression genetics: differential display. In Expression Genetics: Differential Display (eds A.B. Pardee & M. McClelland), pp. 1-7. Eaton Publishing, Westborough, MA, USA.

Riechmann, J. L., J. Heard, G. Martin, L. Reuber, C. Jiang, J. Keddie, L. Adam, O. Pineda, O. J. Ratcliffe, R. R. Samaha, R. Creelman, M. Pilgrim, P. Broun, J. Z. Zhang, D. Ghandehari, B. K. Sherman and G. Yu (2000). Arabidopsis transcrip- tion factor: genome wide compara- tive analysis among eukaryotes. Science, 290: 2105-2110.

Roshandel, P. (2007). The possible in- volvement of Myb, Wak and Rim2 proteins in salt tolerance in rice. Indian Journal of Plant Physiology, 12: 215-221.

Salisbury, F. B. and C. W. Ross (1989). Plant Physiology. 3rd ed. Wadsworth Publishing Company, Belmont, CA, USA.

Sambrook, J., E. F. Fritsch, and T. Mani- atis (2001). Molecular Cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY). Volume 1, Third edition, 1: 116-118.

Serrano, R., J. M. Mulet, G. Rios, J. A. Marquez, I. F. de Larrinoa, M. P. Leube, I. Mendizabal, A. Pascual- Ahuir, M. Proft, R. Ros and C. Montesinos (1999). A glimpse of the mechanisms of ion homeostasis during salt stress. J. Exp. Bot., 50:1023-1036.

Shokry, A., F. M. Abdel-Tawab, A. Bahieldin, Hala F. Eissa, O. M. Saleh and Gh. A. Gad El-Karim (2007). Functional Genomics for salt tolerance in rice (oryza sativa L.). Egypt. J. Genet. Cytol., 36:207-217.

Terol, J., C. Domingo and M. Talon (2006). The GH3 family in plants: genome wide analysis in rice and evolutionary history based on EST analysis. Gene, 371: 279-290.

Vos, P., R. Hogers, M. Bleeker, M. Reijans, T. Van de Lee, M. Hornes, A. Freijters, J. Pot, J. Peleman, M. Kuiper and M. Zabeau (1995). AFLP: a new technique for DNA fingerprinting. Nuc. Acids Res., 23: 4407-4414.

Zhu, J. K. (2001). Plant salt tolerance. Trends Plant Sci., 6: 66-71.

Downloads

Published

2016-01-08

Issue

Section

Articles

Most read articles by the same author(s)

1 2 > >>