Isolation and Characterization of Cab8 Gene from Wild Vicia Cinera Species

Authors

  • RANIA M. ABOU ALI Agricultural Genetic Engineering Research Institute (AGERI), ARC, Giza, Egypt
  • MENNATALLAH M. EL-HEFNAWY October University for Modern Sciences and Arts (MSA), 6 October City, Egypt
  • A. M. K. NADA Agricultural Genetic Engineering Research Institute (AGERI), ARC, Giza, Egypt October University for Modern Sciences and Arts (MSA), 6 October City, Egypt

Abstract

Drought stress is a limiting factor to the agricultural productivity in tropical, semi-arid and arid regions. More than
95% of Egypt’s land is desert, while less than 3% is confined to farming and agriculture. Drought stress causes cellular water deficits, which results in the loss of turgor, change in cell volume, change in membrane integrity, concentration of solutes, denaturation of proteins and several physiological and molecular components (Bartels and Souer, 2003; Griffiths and Parry, 2002; Lawlor and Cornic, 2002; Parry et al., 2002; Raymond and Smirnoff, 2002). Under such severe conditions, cells need to induce gene(s) producing some products that may act to sustain the cellular functions through osmotic adjustments and cellular structure protection (Bray, 2002).
High drought conditions and high light intensity from the sun is very damaging to plants subjected to these conditions. The morphology, molecular and biochemical characteristics of the plant structure contribute to maximizing the photon capture and their use in CO2 fixation (Larcher, 1995).
Photooxidative stress was known to be the cause of the oxidative stress, but it has been proven that it also results from drought and salinity stresses. Oxidative stress is characterized by the accumulation of harmful reactive oxygen species (ROS) in plant tissues, and it is one of the most deleterious stresses. Most of the environmental stresses result in the overproduction of ROS, which consequently causes an oxidative stress. The reaction of ROS with lipids and proteins results in the fast accumulation of toxic products, which brings severe damage to the plants. One of these toxic products is lipid peroxide which causes cellular damage (Chia et al., 1984; Dhindsa et al., 1981).

References

Altschul, S. F., T. L. Madden, A. A. Schaffer, J. H. Zhang, Z. Zhang, W. Miller, D. J. Lipman (1997). Gapped BLAST and PSI-BLAST: a new generation of protein data- base search programs. Nucleic Ac- ids Research, 25: 3389-3402.

Bartels, D. and E. Souer (2003). Molecu- lar responses of higher plants to dehydration. Plant responses to ab- iotic stress. Topics in Current Ge- netics. Berlin; Springer; 4: 9-38.

Bray, E. A. (2002). Classification of genes differentially expressed during water-deficit stress in Arabidopsis thaliana: an analysis using mi- croarray and differential expression data. Ann. Bot., 89: 803-811.

Chia, L. S., C. I. Mayfeld and J. E. Thompson (1984). Simulated acid rain induces lipid peroxidation and membrane damage in foliage. Plant Cell Environ., 7: 333-338.

Dhindsa, R. S., P. Plumb-Dhindsa and T. A. Thorpe (1981). Leaf senes- cence: correlated with increased levels of membrane permeability and lipid peroxidation, and de- creased levels of superoxide dis- mutase and catalase. J. Exp. Bot., 32: 93-101.

Diab A. A., A. Ageez, B. A. Abdelgawad and T. Z. Salem (2007). Cloning, sequence analysis and in silico mapping of a drought-inducible gene coding for s- adenosylmethionine decarboxylase from durum wheat. World Applied Sciences J., 2: 333-340.

Gepts P, W. Beavis, E. Brummer, R., Shoemaker H. Stalker, N. Weeden and N. Young (2005). Legumes as a Model Plant Family. Genomics for Food and Feed Report of the Cross-Legume Advances through Genomics Conference. Plant Physiology, 137: 1228-1235.

Griffiths, H. and M. A. J. Parry (2002). Plant responses to water stress. Ann. Bot., 89: 801-802.

Jurgen, K. (1992). Identification of the photosystem I antenna polypep- tides in barley. Isolation of three pigment-binding antenna com- plexes. Eur. J. Biochem., 206: 209-215.

Kalo, P., A. Seres, S. A. Taylor, J. Jakab, Z. Kevei, A. Kereszt, G. Endre, T. H. N. Ellis and G. B Kiss. (2004). Comparative mapping between Medicago sativa and Pisum sati- vum. Mol. Genet. Genome, 272:235-246.

Larcher, W. (1995). Plant under stress. Physiological Plant Ecology. Ed. 3rd. Springer. Berlin., pp321-448.

Lawlor, D. W. and G. Cornic (2002). Pho- tosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant Cell Environ., 25: 275-294.

Lee, J. M., D. Grant, C. E. Vallejos and R. C. Shoemaker (2001). Genome or- ganization in dicots. II. Arabidop- sis as a ‘‘bridging species’’ to re- solve genome evolution events among legumes. Theor. Appl. Genet., 103: 765-773.

O’Rourke, E. J., C. Chevalier, S. Boiteux, A. Labigne, L. Ielpi and J. P. Radi- cella (2000). A novel 3- methyladenine DNA glycosylase from Helicobacter pylori defines a new class within the endonuclease III family of base excision repair glycosylases. J. Biol. Chem., 275: 20077-20083.

Parry, M. A. J., P. J. Andralojc, S. Khan, , P. J. Lea and A. J. Keys (2002). Rubisco activity: effects of drought stress. Ann. Bot., 89: 833-839.

Raymond, M. J. and N Smirnoff (2002). Proline metabolism and transport in maize seedlings at low water po- tential. Ann. Bot., 89: 813-823.

Saitou, N. and M. Nei (1987). The neigh- borjoining method: a new method for reconstructing phylogenetic trees. Mol.Biol. Evol., 4: 406-425.

Sambrook, J., E. F. Fritsch and T Mani- atis. (1989). Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.

Thompson, J. D., D. G. Higgins and T. J. Gibson (1994). CLUSTAL W: im- proving the sensitivity of progres- sive multiple sequence alignment through sequence weighting, posi- tions-specific gap penalties and weight matrix choice. Nucleic Ac- ids Res., 22: 4673-4680.

Wang J., H. Zhang and H. Goodman (1994). An Arabidopsis Cab gene homologous to Cab-8 of tomato. Plant Physiol., 104: 297

Wojciechowski, M. F., M. Lavin and M. J. Sanderson (2004). A phylogeny of legumes (Leguminosae) based on analyses of the plastid matK gene resolves many well-supported sub- clades within the family. Am. J. Bot., 91: 1846-1862.

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2016-01-08

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