Identification and Study of cis regulatory elements and phylogenetic relationship of TaSRG and other salt response genes

Paper Details

Research Paper 01/07/2014
Views (588)
current_issue_feature_image
publication_file

Identification and Study of cis regulatory elements and phylogenetic relationship of TaSRG and other salt response genes

Sirvan Saeediazar, Hamid Najafi Zarrini, Gholamali Ranjbar, Parviz Heidari
J. Biodiv. & Environ. Sci. 5(1), 1-5, July 2014.
Copyright Statement: Copyright 2014; The Author(s).
License: CC BY-NC 4.0

Abstract

Salt stress is the major limiting factor in agriculture that affects on all developmental stages including germination, seedling and vegetative stages. Under salt stress, induce the expression of many plant genes. These genes encode the defending proteins, and regulatory proteins that regulate the stress signal transduction. The TFs interact with cis-elements in the promoter regions of several stress-related genes and thus up-regulate the expression of many downstream genes resulting in imparting abiotic stress tolerance. The identification of cis-regulatory DNA elements responsive to stress is important for studying gene regulation and for biotechnological applications. In this study, we identified cis-regulatory elements and also investigated the phylogenetic relationship of salt response genes of wheat, rice, barley, maize and Arabidopsis. The result of phylogenetic tree showed that TaSRG, LTP and IPK2 genes have located in one branch. The analysis of 5´UTR of salt response genes showed four elements have the most frequencies that including, TATA Box (24.55%), Unnamed-4 (24.55%), CAAT Box (17.43%) and SP1(5.33%), respectively. The TaSRG gene also is a cis elements-rich gene in which TATA Box (5′-TATAAA-3′) and CAAT (5′-CAAT-3′) Box have most frequencies. The most important identified cis regulatory elements in response to stress are ABRE, G-box, MBS, TGA-element. This results indicated that gene expression control in different checkpoints of cell cycle may be dependent to both the frequency of enhancers and stress responsive cis regulatory elements under abnormal conditions.

Agarwal PK, Jha B. 2010. Transcription factors in plants and ABA dependent and independent abiotic stress signaling. Biologia Plantarum 54, 201-212.

Chandna R, Azooz MM, Ahmad P. 2013. Recent Advances of Metabolomics to Reveal Plant Response During Salt Stress. In: Ahmad P, Azooz MM, Prasad MNV, eds. Salt Stress in Plants. NewYork, US: Springer publishing, 1-14 P.

Dare AP, Schaffer RJ, Wang KL, Allan AC, Hellens RP. 2008. Identification of a cis-regulatory element by transient analysis of co-ordinately regulated genes. Plant Methods 4(17), 1-10.

He X, Hou X, Shen Y, Huang Z. 2011.TaSRG, a wheat transcription factor, significantly affects salt tolerance in transgenic rice and Arabidopsis. FEBS Letters 585, 1231-1237.

Ibraheem O, Bothab CEJ, Bradley G. 2010. In silico analysis of cis-acting regulatory elements in 5‘regulatory regions of sucrose transporter gene families in rice (Oryza sativa Japonica) and Arabidopsis thaliana. Computational Biology and Chemistry 34, 268-283.

Lata C, Yadav A, Prasad M. 2011. Role of plant transcription factors in abiotic stress tolerance. In: Shanker A and Venkateshwarulu B, eds. Abiotic Stress Response in Plants, INTECH Open Access Publishers, 269-296 P.

Priest HD, Filichkin SA, Mockler TC. 2009. cis-Regulatory elements in plant cell signaling. Current Opinion in Plant Biology 12, 643–649.

Sadegh Nejad E, Askari H, Hamzelou S, Gholami M. 2013. Regulation of core cell cycle genes by cis-regulatory elements in Arabidopsis thaliana. Plant Knowledge Journal 2(2), 69-75.

Tajrishi MM, Tuteja N. 2011. Isolation and in silico analysis of promoter of a high salinity stress-regulated pea DNA helicase 45. Plant Signaling & Behavior 6(10), 1447-1450.

Wittkopp PJ, Kalay G. 2012. Cis-regulatory elements: molecular mechanisms and evolutionary processes underlying divergence. Nature Reviews Genetics 13, 59-69.

Won SK, Lee YJ, Heo YK, Cho M, Chocis HT. 2009. Element and Transcriptome Based Screening of Root Hair-Specific Genes and Their Functional Characterization in Arabidopsis. Plant Physiology 150, 1459–1473.

Related Articles

Bacteriological analysis of selected fishes sold in wet markets in Tuguegarao city, Cagayan, Philippines

Lara Melissa G. Luis, Jay Andrea Vea D. Israel, Dorina D. Sabatin, Gina M. Zamora, Julius T. Capili, J. Biodiv. & Environ. Sci. 27(2), 1-9, August 2025.

Effect of different substrates on the domestication of Saba comorensis (Bojer) Pichon (Apocynaceae), a spontaneous plant used in agroforestry system

Claude Bernard Aké*1, Bi Irié Honoré Ta2, Adjo Annie Yvette Assalé1, Yao Sadaiou Sabas Barima1, J. Biodiv. & Environ. Sci. 27(1), 90-96, July 2025.

Determinants of tree resource consumption around Mont Sangbé national park in western Côte d’Ivoire

Kouamé Christophe Koffi, Serge Cherry Piba, Kouakou Hilaire Bohoussou, Naomie Ouffoue, Alex Beda, J. Biodiv. & Environ. Sci. 27(1), 71-81, July 2025.

Fishing ground and seasonal availability of diamondback squid (Thysanoteuthis rhombus) along southern Tañon Strait: Local fishermen’s insights

Robinson S. Amihan Jr., Hannah Abigail R. Daita, J. Biodiv. & Environ. Sci. 27(1), 61-70, July 2025.

Characteristics of the mycobiota of cultivated plants grown in the Kur-Araz valley according to ecolo-trophic relationships

Anakhanum Yusifova, Sanubar Aslanova, Basti Asadova, Irada Mammadova, Aytan Safarova, J. Biodiv. & Environ. Sci. 27(1), 55-60, July 2025.

Screening of an medicinal plant Crinum asiaticum L. bulb extracts for their proximate composition, phytochemical analysis and antioxidant activity

K. Gowthaman, P. Prakash, V. Ambikapathy, S. Babu, A. Panneerselvam, J. Biodiv. & Environ. Sci. 27(1), 41-54, July 2025.

Immunomodulatory effect of Panchagavya and Lactobacillus probiotics on Oreochromis mossambicus (W. K. H. Peters)

R. Keerthiga, M. Kannahi, J. Biodiv. & Environ. Sci. 27(1), 30-40, July 2025.