An Accurate Representation of the Number of bZIP Transcription Factors in the Triticum aestivum (Wheat) Genome and the Regulation of Functional Genes during Salt Stress

• Published in: Current issues in molecular biology Vol. 46; no. 5; pp. 4417 - 4436
• Main Authors: Liu, Xin, Sukumaran, Selvakumar, Viitanen, Esteri, Naik, Nupur, Hassan, Sameer, Aronsson, Henrik
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 07.05.2024
• Subjects: BARI Gom-25; Biological Sciences; Biologiska vetenskaper; bZIP; salinity; salt stress; transcription factor; wheat; salinity; transcription factor; bZIP; salt stress; wheat; BARI Gom-25
• ISSN: 1467-3045; 1467-3037; 1467-3045
• DOI: 10.3390/cimb46050268

Climate change is dramatically increasing the overall area of saline soils around the world, which is increasing by approximately two million hectares each year. Soil salinity decreases crop yields and, thereby, makes farming less profitable, potentially causing increased poverty and hunger in many areas. A solution to this problem is increasing the salt tolerance of crop plants. Transcription factors (TFs) within crop plants represent a key to understanding salt tolerance, as these proteins play important roles in the regulation of functional genes linked to salt stress. The basic leucine zipper (bZIP) TF has a well-documented role in the regulation of salt tolerance. To better understand how bZIP TFs are linked to salt tolerance, we performed a genome-wide analysis in wheat using the Chinese spring wheat genome, which has been assembled by the International Wheat Genome Sequencing Consortium. We identified 89 additional bZIP gene sequences, which brings the total of bZIP gene sequences in wheat to 237. The majority of these 237 sequences included a single bZIP protein domain; however, different combinations of five other domains also exist. The bZIP proteins are divided into ten subfamily groups. Using an in silico analysis, we identified five bZIP genes ( , , , , and ) that were involved in regulating salt stress. By scrutinizing the binding properties to the 2000 bp upstream region, we identified putative functional genes under the regulation of these TFs. Expression analyses of plant tissue that had been treated with or without 100 mM NaCl revealed variable patterns between the TFs and functional genes. For example, an increased expression of was correlated with an increased expression of the corresponding functional genes in both root and shoot tissues, whereas downregulation in root tissues strongly decreased the expression of two functional genes. Identifying strategies to sustain the expression of the functional genes described in this study could enhance wheat's salt tolerance.